- T Cell Subsets in Renal Transplant Rejection
- HLA Typing with Matching of the Recipient and an Allograft Donor
- Types of Transplant Rejection Based on the Time to Onset
- Clinical Severity of Reaction in Food Allergy
- Risk Factors for Severe Reaction in Peanut Allergy
- Symptom Score of Verwimp et al for Cow's Milk Protein Intolerance in Infants
- Grading Reaction Severity in Peanut and Nut Allergy
- Recommendations of Bock et al for Reducing the Risk of a Food-Related Allergic Reaction in a School
- Equations of Vanto et al for Predicting Tolerance to Milk By 4 Years of Age in an Infant with Cow's Milk Hypersensitivity
- Conditions That Can Be Confused with a Food Allergy
- Cross Reactions Between Fruits and Vegetables with Airborne Pollens
- Food Protein-Induced Enterocolitis Syndrome (FPIES) in Infants and Young Children
- Inhalation of a Food Allergen
- Risk Factors of Nowak-Wegrzyn et al for a Reaction During an Oral Food Challenge
- When To and Not To Perform an Oral Food Challenge
- Kiss-Induced Allergic Symptoms Associated with a Food Allergy
- Clinical Findings Associated with Cow's Milk Allergy in an Infant
- Pulmonary Disease Associated with Cow Milk Allergy in Infants (Heiner Syndrome, Cow Milk-Induced Pulmonary Hemosiderosis)
- Pork-Cat Syndrome
- Allergy to Galactose-[alpha]-1,3-Galactose (alpha Gal) and Allergy to Meat
- Risk Factors for Hidden Food Allergens
- Food Protein-Induced Enterocolitis Syndrome (FPIES) Associated with Rice
- Clinical Findings of Elizur et al That Can Help to Identify an Infant Mislabelled As Having Cow Milk Allergy
- Types of Cow Milk Allergy (CMA)
- CSF-to-Serum Albumin Index and the Intactness of the Blood-Brain Barrier
- CSF IgG-to-Albumin Ratio and CNS Production of Antibody
- CSF-to-Serum IgG Index and CNS Production of Antibody
- CSF IgG Index
- CNS IgG Synthesis Rate
- CSF Kappa and Lambda Free Light Chain (KFLC and LFLC) Indices
- Criteria of Holmes et al for the Diagnosis of the Chronic Fatigue Immune Dysfunction Syndrome
- Prognostic Factors of Hartz et al for Patients with the Chronic Fatigue Syndrome
- Oxford Research Criteria for the Diagnosis of the Chronic Fatigue Syndrome
- Criteria of Fukuda et al for Chronic Fatigue Syndrome (International Chronic Fatigue Syndrome Study Group)
- Oxford Research Criteria for Post-Infectious Fatigue Syndrome (PIFS)
- Ratio of Kappa-to-Lambda Light Chains in the Serum
- Relative Staining of Kappa-to-Lambda Light Chains in Bone Marrow Biopsies
- Criteria for Decreased Levels of Serum Immunoglobulin A (IgA Deficiency States)
- Differential Diagnosis of Marked Hypergammaglobulinemia
- Patterns of Immunofluorescent Antinuclear Antibodies (ANA)
- Clinical Indications for Measurement of Anti-Neutrophil Cytoplasmic Antibodies (ANCA)
- Conditions Associated with a Positive Assay for Rheumatoid Factor (RF)
- 1982 ACR Criteria for the Diagnosis of Systemic Lupus Erythematosus
- Systemic Lupus Erythematosus Disease Activity Index (SLEDAI)
- SLICC/ACR Damage Index for Systemic Lupus Erythematosus
- The Lupus Activity Criteria Count (LACC)
- Systemic Lupus Activity Measure (SLAM)
- Flare Severity Score of Lockshin et al for Patients with Systemic Lupus Erythematosus
- The Activity Index of le Riche for Systemic Lupus Erythematosus
- The Neonatal Lupus Syndromes
- The SELENA Flare Tool
- Diagnostic Features of Drug-Induced Lupus Erythematosus (DIL)
- Risk Factors for Drug-Induced Lupus Erythematosus
- Management of a Patient with Drug-Induced Lupus Erythematosus
- The European Consensus Lupus Activity Measurement (ECLAM)
- Model of Ward et al for Predicting In-Hospital Mortality for a Patient with Systemic Lupus Erythematosus (SLE)
- Clinical Features of Protein-Losing Enteropathy in a Patient with Systemic Lupus Erythematosus
- Criteria of Zeitouni et al for Rowell's Syndrome (Lupus Erythematosus with Erythema multiforme-like Skin Lesions)
- Total Activity Score of the Cutaneous LE Disease Area and Severity Index (CLASI)
- Total Damage Score of the Cutaneous LE Disease Area and Severity Index (CLASI)
- British Isles Lupus Assessment Group (BILAG) Index
- The Revised British Isles Lupus Assessment Group (BILAG) Index 2004
- Risk Factors of Yip et al for Left Ventricular Systolic Dysfunction in a Patient with Systemic Lupus Erythematosus (SLE)
- University College Hospital (UCH) and Middlesex Score for Disease Activity in Systemic Lupus Erythematosus (SLE)
- Grading Organ Involvement for the University College Hospital (UCH) and Middlesex Score for Disease Activity in Systemic Lupus Erythematosus (SLE)
- The BILAG Categories for General Non-Specific Manifestations of SLE
- The BILAG Categories for Mucocutaneous Manifestations of SLE
- The BILAG Categories for Musculoskeletal Manifestations of SLE
- The BILAG Categories for Cardiovascular and Respiratory Manifestations of SLE
- The BILAG Categories for Vasculitis Manifestations of SLE
- The BILAG Categories for Hematological Manifestations of SLE
- The BILAG Categories for Nervous System Manifestations of SLE Identified on the Initial Assessment
- The BILAG Categories for Nervous System Manifestations of SLE Identified on a Followup Assessment
- The BILAG Categories for Renal Manifestations of SLE Identified on the Initial Assessment
- The BILAG Categories for Renal Manifestations of SLE on a Followup Assessment: Proteinuria
- The BILAG Categories for Renal Manifestations of SLE on a Followup Assessment: Hypertension and Renal Function
- The BILAG Categories for Renal Manifestations of SLE on a Followup Assessment: Final Diagnosis
- Risk Factors of Karassa et al for Central Nervous System (CNS) Involvement in a Patient with Systemic Lupus Erythematosus
- ANA Negative Systemic Lupus Erythematosus (SLE)
- Psychosis and Visceral Involvement in a Patient with Systemic Lupus Erythematosus and Anti-Ribosomal P Protein Antibody
- Clinical Features of Mucosal Lupus Erythematosus
- Clinical Features of Chilblain Lupus Erythematosus Hutchinson
- Alopecia and Other Changes in Hair Associated with Lupus Erythematosus
- Use of the BILAG Index to Define a Lupus Flare
- Severity of CNS Changes on Cranial MRI in a Patient Systemic Lupus Erythematosus
- Neuropsychiatric Syndromes in Systemic Lupus Erythematosus (SLE)
- Risk Factors of Tomietto et al for Cognitive Impairment in Systemic Lupus Erythematosus (SLE)
- Risk Factors of Mikdashi et al for Epilepsy in a Patient with Systemic Lupus Erythematosus (SLE)
- Shrinking Lungs Syndrome (SLS) in a Patient with Systemic Lupus Erythematosus
- Acute Reversible Hypoxia Syndrome in a Patient with Systemic Lupus Erythematosus
- Clinical Features of Acute Lupus Pneumonitis
- Lupus Demylinating Syndrome (Lupoid Sclerosis)
- Risk Factors of Mikdashi et al for Ischemic Stroke in a Patient with Systemic Lupus Erythematosus
- Rhupus Syndrome
- Modified Classification of Saketkoo and Quinet for Lupus Arthropathy
- Index of van Vugt et al for Jaccoud’s Arthropathy
- Flow Diagram of van Vugt et al for Classifying a Patient with SLE and a Deforming Arthropathy
- Clinical and Laboratory Features of a Patient with Systemic Lupus Erythematosus (SLE) and Biopsy-Proven Myositis
- American Rheumatism Association (ARA) Criteria for the Diagnosis of Rheumatoid Arthritis
- Classification Tree for Diagnosis of Rheumatoid Arthritis
- The Rheumatoid Arthritis Disease Activity Index (RADAI)
- Criteria of Pinals et al for Complete Clinical Remission in Rheumatoid Arthritis
- Felty's Syndrome
- Issues Impacting the Decision to Use Second Line Drugs in the Management of a Patient with Rheumatoid Arthritis
- Criteria of Steinbrocker et al for Therapeutic Response in a Patient with Rheumatoid Arthritis
- The Index of Mallya and Mace for Disease Activity in Rheumatoid Arthritis
- Rheumatoid Arthritis Disease Activity Scores (DAS) of van der Heijde et al
- Disease Activity Index of Scott for Evaluating Improvement Following Treatment of Rheumatoid Arthritis
- Algorithm of Fehring and Brooks for Treatment of a Patient with Rheumatoid Arthritis and Neck Pain
- Sakaguchi-Kauppi Method to Screen for Vertical Atlantoaxial Dislocation in a Patient with Rheumatoid Arthritis
- The PIP Joint Synovitis Score for a Patient with Rheumatoid Arthritis
- The Stoke Index of Davis et al for Measuring Disease Activity in a Patient with Rheumatoid Arthritis
- Algorithm of Brennan et al for Predicting the Risk of Developing Radiological Erosions in a Patient with Early Rheumatoid Arthritis
- Articular Index (AI) Score of Ritchie et al for a Patient with Rheumatoid Arthritis
- Clinical Practice Decision Tree of the French Society of Rheumatology for the First Disease Modifying Antirheumatic Drug in Very Early Rheumatoid Arthritis
- Decision Tree of Nell et al for Identifying the Risk of Developing Erosive Disease in a Patient with Early Arthritis
- Disease Activity Score of Prevoo et al for Rheumatoid Arthritis Based on Separate 28 Joint Counts for Tender and Swollen Joints (DAS28, DAS28T+S, DAS28 ESR)
- The Index of Lansbury and Haut for Quantifying the Total Joint Inflammation and Deformity in a Patient with Rheumatoid Arthritis
- Grades of Larsen for Radiographic Changes in Rheumatoid Arthritis
- American College of Rheumatology Criteria for Improvement in Rheumatoid Arthritis Based on a 20 Percent Improvement in the Core Data Set (ACR20)
- EULAR Therapeutic Response Criteria in a Patient with Rheumatoid Arthritis Based on the Change in DAS28 or DAS Scores
- Model of Drossaers-Bakker et al for Identifying a Patient at Risk for Severe Rheumatoid Arthritis Within 12 Years Based on Baseline Parameters
- Classification of Pellicci et al for Rheumatoid Arthritis Affecting the Cervical Spine
- Indications of Bouchaud-Chabot and Liote for Surgery in a Patient with Rheumatoid Arthritis Involving the Cervical Spine
- 2009 ACR/EULAR Criteria for Rheumatoid Arthritis
- DAS28 Scores Using C-Reactive Protein (DAS28 CRP)
- DAS Scores Using C-Reactive Protein (DAS CRP)
- RAPID3 (Routine Assessment of Patient Index Data 3)
- 2010 American College of Rheumatology (ACR) and European League Against Rheumatism (EULAR) Classification Criteria for Rheumatoid Arthritis
- Indications for Considering a Total Joint Arthroplasty in a Patient with Rheumatoid Arthritis
- Semiquantitative Scales of Szkudlarek et al to Describe the Ultrasonographic Changes in Joints Affected by Rheumatoid Arthritis
- Rheumatoid Meningitis
- The Simplified Disease Activity Index (SDAI) and Clinical Disease Activity Index (CDAI) for a Patient with Rheumatoid Arthritis
- American College of Rheumatology (ACR) and European League Against Rheumatism (EULAR) Criteria for Remission in Rheumatoid Arthritis for a Clinical Trial
- 7 Joint Ultrasound Score of Backhaus et al (German US7 Score) : Subscore for Erosions
- 7 Joint Ultrasound Score of Backhaus et al (German US7 Score): Subscore for Tenosynovitis and Paratendonitis
- 7 Joint Ultrasound Score of Backhaus et al (German US7 Score): Subscore for Synovitis Using Gray-Scale Ultrasound (GSUS)
- 7 Joint Ultrasound Score of Backhaus et al (German US7 Score): Subscore for Synovitis Using Power Doppler Ultrasound (PDUS)
- Algorithm of Nam et al for Management of a Patient with Early Inflammatory Arthritis
- American College of Rheumatology (ACR) Criteria for Polyarteritis Nodosa
- Classification Tree for the Diagnosis of Polyarteritis Nodosa
- Criteria of Ozen et al for Diagnosis of Polyarteritis Nodosa in Childhood
- Criteria for Polyarteritis Nodosa from the International Consensus Conference on the Nomenclature of Systemic Vasculitis (Chapel Hill Conference)
- Clinical Features of Polyarteritis Nodosa Associated with Viral Hepatitis B
- Polyarteritis Nodosa in a Neonate Born to a Mother with Polyarteritis Nodosa
- American College of Rheumatology (ACR) Criteria for the Diagnosis of Churg-Strauss Syndrome
- Classification Tree for the Diagnosis of Churg-Strauss Syndrome
- Criteria for Churg-Strauss Syndrome from the International Consensus Conference on the Nomenclature of Systemic Vasculitis (Chapel Hill Conference)
- Clinical Features of Churg-Strauss Syndrome
- American College of Rheumatology (ACR) Criteria for the Diagnosis of Wegener's Granulomatosis
- Classification Tree for the Diagnosis of Wegener's Granulomatosis
- Histologic Diagnosis of Wegener's Granulomatosis Based on Biopsy from the Head and Neck
- Criteria for a Major Exacerbation of Wegener's Granulomatosis
- Disease Activity Index for Wegener's Granulomatosis
- Histopathologic Findings of Matsubara et al in a Nasal Biopsy from a Patient with Wegener's Granulomatosis
- Criteria for Wegener's Granulomatosis from the International Consensus Conference on the Nomenclature of Systemic Vasculitis (Chapel Hill Conference)
- Prognostic Features for a Patient with Wegener's Granulomatosis
- Prognostic Factors of Slot et al for a Patient with PR3-ANCA Associated Vasculitis with Renal Involvement
- Clinical and Laboratory Findings Associated with Wegener's Granulomatosis
- Criteria for Limited Wegener's Granulomatosis from the Wegener's Granulomatosis Etanercept Trial
- ELK Classification of DeRemee et al for Wegener's Granulomatosis
- Modified ELK Score of Reinhold-Keller et al for Describing the Extent of Wegener's Granulomatosis
- Predictors of Kamali et al for Survival in a Patient with Wegener's Granulomatosis
- Modified Birmingham Vasculitis Activity Score (BVAS) for Wegener's Granulomatosis
- American College of Rheumatology (ACR) Criteria for the Diagnosis of Temporal (Giant Cell) Arteritis
- Classification Tree for the Diagnosis of Temporal (Giant Cell) Arteritis
- Criteria of Chuang et al for Polymyalgia Rheumatica
- Criteria of Healey for Polymyalgia Rheumatica
- Criteria for Large Vessel Vasculitis (Giant Cell vs Takayasu Arteritis) from the International Consensus Conference on the Nomenclature of Systemic Vasculitis (Chapel Hill Conference)
- Criteria of Bird et al for Polymyalgia Rheumatica
- Risk Factors of Larsson et al for Giant Cell Arteritis in Women
- Algorithm of Shmerling for a Patient with Possible Temporal Arteritis
- Risk Factors of Nesher et al for Cranial Ischemic Complications in a Patient with Giant Cell Arteritis
- Clinical Features of Temporal (Giant Cell) Arteritis
- Temporal Artery Biopsy Formula of Younge et al
- Reasons for a False Negative Temporal Artery Biopsy in a Patient with Giant Cell Arteritis
- Algorithm of Hellman and Hunder for Using Color Doppler Ultrasonography in the Evaluation of a Patient Suspected of Having Giant Cell Arteritis
- 2012 EULAR/ACR Scoring Algorithm for Polymyalgia Rheumatica (PMR)
- Patient Factors of Breuer et al Associated with the Diagnosis of Giant Cell Arteritis Following a Negative Temporal Artery Biopsy
- Indications of Alberts and Mosen for Performing a Temporal Artery Biopsy Following Duplex Ultrasonography
- American College of Rheumatology (ACR) Criteria for the Diagnosis of Hypersensitivity Vasculitis
- Classification Tree for the Diagnosis of Hypersensitivity Vasculitis
- Criteria for Cutaneous Leukocytoclastic Angiitis from the International Consensus Conference on the Nomenclature of Systemic Vasculitis (Chapel Hill Conference)
- American College of Rheumatology (ACR) Criteria for the Diagnosis of Henoch-Schonlein Purpura
- Classification Tree for the Diagnosis of Henoch-Schonlein Purpura
- Criteria for Henoch-Schonlein Purpura from the International Consensus Conference on the Nomenclature of Systemic Vasculitis (Chapel Hill Conference)
- American College of Rheumatology (ACR) Criteria for the Diagnosis of Takayasu Arteritis
- Classification Tree for the Diagnosis of Takayasu Arteritis
- Criteria of Ishikawa for the Diagnosis of Takayasu Arteritis
- Criteria of Sharma et al for the Diagnosis of Takayasu Arteritis
- Criteria of Kerr et al for Active Takayasu Arteritis
- Criteria for the Diagnosis of Behcet’s Disease from the International Study Group for Behcet’s Disease
- Diagnostic Criteria for Behcet’s Syndrome from the Behcet’s Disease Research Committee of Japan
- Behcet's Disease Activity Index of Lawton et al
- Mouth and Genital Ulcers with Inflamed Cartilage (MAGIC Syndrome)
- Clinical and Laboratory Findings in Neuro-Behcet's Disease
- Findings Suggesting a Poor Prognosis in a Patient with Neuro-Behcet's Disease
- Criteria of Dilsen et al for the Skin Pathergy Test (SPT) in Behcet’s Disease
- Pseudo-Behcet Syndrome
- Disease Activity Index for Intestinal Behcet’s Disease (DAIBD) of Cheon et al
- Monitoring the Change in the Disease Activity Index for Intestinal Behcet’s Disease (DAIBD) Over Time
- Clinical Stage and Grade of Acute GVHD by Glucksberg et al
- International Bone Marrow Transplant Registry (IBMTR) Severity Index for Grading Acute Graft versus Host Disease
- Histopathologic Grading of Acute Graft versus Host Disease
- Acute Graft versus Host Activity Index (aGVHDAI) of Leisenring et al
- Prognostic Factor Score of Akpek et al for a Patient with Chronic Graft-versus-Host Disease (GVHD)
- Indications of Irani et al for Requesting a Surgical Consult in a Patient with Severe Acute Gastrointestinal Graft-versus-Host Disease (GVHD)
- Risk Factors of Jacobsohn et al for Overall Survival in a Child with Chronic Graft-versus-Host Disease (GVHD) Following Allogeneic Hematopoietic Stem Cell Transplant (HSCT)
- Criteria for the Diagnosis of Sjogren's Syndrome
- Histologic Grading of a Labial Salivary Gland Biopsy in Patients with Sjogren's Syndrome
- Criteria of Fox et al for Sjogren's Syndrome (La Jolla or California Criteria)
- Criteria of Homma et al for Sjogren's Syndrome (Japanese Ministry of Health and Welfare)
- Criteria of Segerberg-Konttinen et al for Sjogren's Syndrome
- Criteria of Skopouli et al for Sjogren's Syndrome (Greek Criteria)
- Criteria of Manthorpe et al for Sjogren's Syndrome (Copenhagen Criteria)
- Criteria of Vitali et al for Sjogren's Syndrome (Preliminary European Criteria)
- Classification Tree of Vitali et al for Primary Sjogren's Syndrome
- Exclusion Conditions in the Diagnosis of Sjogren's Syndrome
- Sjogren's Syndrome Disease Damage Index (SSDDI)
- Sjogren's Syndrome Disease Activity Index (SSDAI)
- Ultrasonographic Score of Hocevar et al for the Major Salivary Glands in Primary Sjogren's Syndrome
- Classification of Makula et al for Ultrasonographic Changes in the Parotid Gland Associated with Primary Sjogren's Syndrome
- Classification of Niemela et al for Ultrasonographic Changes in Salivary Glands Associated with Primary Sjogren's Syndrome
- Secondary Sjogren's Syndrome Associated with Hepatitis C Virus (HCV)
- Criteria of the Sjogren’s International Collaborative Clinical Alliance (SICCA) Research Groups for Sjogren’s Syndrome
- Criteria of McAdam et al for the Diagnosis of Relapsing Polychondritis
- Systemic Disorders Associated with Relapsing Polychondritis
- Birmingham Vasculitis Activity Score (BVAS)
- Vasculitis Damage Index (VDI)
- Systemic Necrotizing Vasculitis Damage Index (SNVDI)
- The French Five Factor Score (FFS)
- Criteria of Shionoya for Thromboangiitis Obliterans (TAO, Buerger's Disease)
- Vasculitis Associated with Cocaine or Amphetamine Abuse, Including Pseudo-Wegener's Granulomatosis
- Differential Diagnosis of a Pulmonary-Renal Vasculitic Syndrome
- Clinical Features of Degos Syndrome (Malignant Atrophic Papulosis, Lymphocytic Arteriolitis)
- Clinical and Laboratory Features of Schnitzler's Syndrome
- Criteria of Lipsker et al for Schnitzler's Syndrome
- Criteria of Scott and Bacon for Systemic Rheumatoid Vasculitis
- Differential Diagnosis of Small Vessel Vasculitis
- Clinical Classification of the European Vasculitis Study Group (EVSG) for the Disease Severity of an ANCA-Associated Vasculitis
- Causes of Pseudovasculitis
- Criteria for Reiter's Syndrome
- Screening Questionnaire for Ankylosing Spondylitis
- Rome Criteria for Ankylosing Spondylitis
- New York Criteria for Ankylosing Spondylitis
- Modified New York Criteria for Ankylosing Spondylitis
- Criteria of Amor et al for Spondylarthropathy
- The European Spondylarthropathy Study Group (ESSG) Criteria for Spondylarthropathy
- Prediction of Longterm Outcome in Spondyloarthropathy Using the Score of Amor et al
- Disease Activity Index for Reactive Arthritis (DAREA)
- Criteria of Creemers et al for Active Disease in Ankylosing Spondylitis
- Ankylosing Spondylitis Disease Activity Score (AS-DAS) of Creemers et al
- The Bath Ankylosing Spondylitis Disease Activity Index (BASDAI)
- Articular Index of Dougados et al for Patients with Ankylosing Spondylitis
- Criteria of the Ankylosing Spondylitis Working Group for Clinical Remission
- Criteria of the Ankylosing Spondylitis Working Group for Clinical Response to Therapy
- Bath Ankylosing Spondylitis Functional Index (BASFI)
- Mander Enthesis Index (MEI) in Ankylosing Spondylitis
- Reduced Mander Enthesis Index of Heuft-Dorenbosch et al for Ankylosing Spondylitis
- Concise Enthesis Index of Heuft-Dorenbosch et al for Ankylosing Spondylitis (Maastrich Ankylosing Spondylitis Enthesitis Score, MASES)
- Criteria of Sieper and Braun for Reactive Arthritis
- Criteria of the Deutschen Gesellschaft fur Rheumatologie for Reactive Arthritis
- Stoke Ankylosing Spondylitis Spine Score (SASSS)
- Bath Ankylosing Spondylitis Radiology Index (BASRI, BASRI-s)
- MRI Chronicity Index and Activity Index of Bollow et al in a Patient with Sacroiliitis
- Bath Ankylosing Spondylitis Metrology Index (BASMI)
- Modified Schober Index of Macrae and Wright for Measuring Back Flexion
- Early Diagnostic Criteria of Mau et al for Ankylosing Spondylitis
- ILAR (International League of Associations for Rheumatology) Criteria for Juvenile Enthesitis-Related Arthritis
- Prognostic Factors of Leirisalo-Repo for Reactive Arthritis and the Spondyloarthropathies
- Edmonton Ankylosing Spondylitis Metrology Index (EDASMI)
- Clinical Features of Arthritis Associated with Ulcerative Colitis
- Criteria of Rudwaleit et al for Inflammatory Back Pain in a Young to Middle-Aged Adult with Chronic Back Pain
- ASAS Criteria for Inflammatory Back Pain in Patients with Chronic Back Pain
- ASAS Classification Criteria for Axial Spondyloarthritis
- Ankylosing Spondylitis Disease Activity Score (ASDAS) of the Assessment in SpondylArthritis international Society (ASAS)
- Berlin MRI Spine Score for Ankylosing Spondylitis (AS)
- Reactive Arthritis Associated with Tuberculosis (Tuberculous Rheumatism, Poncet’s Disease)
- Risk Factors of Poddubnyy and Sieper for Radiographic Progression in Anklyosing Spondylitis and Axial Spondyloarthritis
- ARA Scleroderma Criteria Cooperative Study Preliminary Clinical Criteria for Systemic Sclerosis
- Hidebinding/Tethering Skin Score of Furst et al for Scleroderma
- Rodnan Score for Progressive Systemic Sclerosis
- Modified Rodnan Skin Score in Scleroderma Using 17 Sites
- Modified Rodnan Skin Score in Scleroderma Using 5 Sites
- Organ System Indices of Furst et al in Systemic Sclerosis
- Kahaleh Skin Score in Scleroderma
- Predictors of Steen et al for Scleroderma Renal Crisis
- Risk Model of Bryan et al for 5 Year Survival in a Patient with Scleroderma
- Criteria of Valentini et al (European Scleroderma Study Group) for Activity of Systemic Sclerosis
- Criteria of Valentini et al (European Scleroderma Study Group) for Activity of Diffuse and Limited Systemic Sclerosis
- Criteria of Steen et al for Scleroderma Renal Crisis
- Classification of Maricq for Changes Seen in the Fingernail Capillaries of a Patient with Scleroderma
- Nailfold Capillary Microscopic Profiles of Joyal et al in a Patient with Systemic Sclerosis
- Criteria of LeRoy and Medsger for Limited Forms of Systemic Sclerosis (lSSc)
- Criteria of LeRoy and Medsger for Limited Cutaneous (lcSSc, CREST Syndrome) or Diffuse Cutaneous Systemic Sclerosis (dcSSc)
- Clinical Features of Occupation-Related Scleroderma
- Criteria of Lally et al for Rapidly (Fulminant) Progressive Systemic Sclerosis
- Clinical Findings Associated with Involvement of the Esophagus or Stomach in Systemic Sclerosis
- Presenting Symptoms of Progressive Systemic Sclerosis
- Criteria of the PRES/ACR/EULAR for the Diagnosis of Juvenile Systemic Sclerosis
- Osteolysis with Bone Resorption in Systemic Sclerosis
- Prognostic Factors of Martini et al for a Patient with Juvenile Systemic Sclerosis
- Diagnostic Clues of Hudson for the Diagnosis of Systemic Sclerosis
- Drug-Induced Scleroderma
- Lung Severity Scale of Medsger et al for a Patient with Systemic Sclerosis
- Cardiac and Vascular Severity Scales of Medsger et al for a Patient with Systemic Sclerosis
- General and Skin Severity Scales of Medsger et al for a Patient with Systemic Sclerosis
- Renal and Gastrointestinal Scales of Medsger et al for a Patient with Systemic Sclerosis
- Joint and Muscle Scales of Medsger et al for a Patient with Systemic Sclerosis
- Prognostic Factors of Hachulla et al for a Patient with Systemic Sclerosis
- Criteria of Penn et al for Scleroderma Renal Crisis
- Factors Associated with a Poor Prognosis for a Patient with Scleroderma Renal Crisis
- Scleroderma Associated with Silica Exposure (Erasmus Syndrome)
- Conditions in the Differential Diagnosis of Scleroderma (Scleroderma-Like Fibrosing Skin Disorders)
- Classification Criteria of Tanimoto et al for Polymyositis and Dermatomyositis
- Childhood Myositis Assessment Scale (CMAS) for the Evaluation of Muscle Function in Juvenile Idiopathic Inflammatory Myopathy
- Prognostic Factors of Benbassat et al for a Patient with Polymyositis or Dermatomyositis
- Criteria of Bohan and Peter for the Diagnosis of Polymyositis and Dermatomyositis
- Overlap Syndrome in a Patient with Dermatomyositis
- Criteria of Marie et al for Remission of Polymyositis or Dermatomyositis
- Prognostic Factors of Marie et al for a Patient with Polymyositis or Dermatomyositis
- Prognostic Factors of Maugars et al for a Patient with Dermatomyositis or Polymyositis
- Risk Factors of Chen et al for Underlying Malignancy in a Patient with Dermatomyositis or Polymyositis
- Dermatomyositis Sine Myositis
- Diagnostic Criteria for Sporadic Inclusion Body Myositis
- Staging the Airway Risk in a Patient with Angioedema
- Triage Algorithm for a Patient with Angioedema of the Head and Neck
- Types of Angioneurotic Edema
- Risk Factors of Kostis et al for Enalapril-Induced Angioedema
- Classification of Kostis et al for the Severity of Angioedema Based on Treatment Intensity
- Criteria of Agostini et al for the Diagnosis of Angioedema Associated with a Deficiency of C1-Inhibitor
- Criteria of Agostoni et al for Determining the Severity of Hereditary Angioedema
- Angioedema Associated with Estrogen Excess
- Clinical Features of Gleich's Syndrome (Episodic Angioedema with Eosinophilia)
- Conditions That May Be Confused with Angioedema
- Persistent, Nonepisodic Angioedema with Eosinophilia of Chikama et al
- Nodules, Eosinophilia, Rheumatism, Dermatitis and Swelling (NERDS)
- Thymidine Incorporation by Lymphocytes and the Stimulation Index (SI)
- Lymphocyte Cytotoxicity (LCT) Assay for Detecting Antibodies to HLA Antigens
- Clinical Classification of Osserman and Genkins for Myasthenia Gravis
- Clinical Crisis in Patients with Myasthenia Gravis
- Predictors of Favorable Response to Thymectomy in Patients with Myasthenia Gravis
- Prognostic Factors of Tellez-Zenteno et al in Patients with Myasthenia Gravis Following Thymectomy
- Clinical Distinction of Myasthenia Gravis from Lambert-Eaton Myasthenic Syndrome
- Clinical Classification of the Myasthenia Gravis Foundation of America (MGFA) for Myasthenia Gravis
- Quantitative Score (QMG) for Disease Severity of the Myasthenia Gravis Foundation of America (MGFA)
- Clinical Score of Besinger et al for a Patient with Myasthenia Gravis
- Ice Pack Test for Evaluating a Patient with Ptosis
- Red Flags of Spillane et al for an Imminent Myasthenic Crisis
- Clinical Features of the Stiff Man Syndrome
- Paraneoplastic Stiff Man Syndrome
- Criteria of Brown and Marsden for the Stiff Man Plus Syndromes
- Progressive Encephalomyelitis with Rigidity
- Jerking Stiff Man Syndrome
- Stiff Limb Syndrome
- Screening Questionnaire for Latex Allergy
- Risk Factors for a Person Having a Latex Allergy
- Clinical Features of Latex Allergy in an Infant
- Bronchoconstriction and Asthma Associated with Latex Allergy
- Healthcare Equipment and Materials That May Contain Natural Rubber Latex (NRL)
- Latex-Fruit Syndrome
- Allergic Reactions to a Latex Condom
- Criteria of Bennett for the Diagnosis of Psoriatic Arthritis
- Risk Factors of Gladman et al for Mortality in Patients with Psoriatic Arthritis
- Classification of Moll and Wright for Psoriatic Arthritis
- Risk Factors of Gladman et al for Identifying a Patient at Diagnosis of Psoriatic Arthritis Who Is at Risk for Disease Progression
- Tool of Helliwell et al for Evaluating Dactylitis in a Patient with Psoriatic Arthritis
- Criteria of Southwood et al for the Diagnosis of Juvenile Psoriatic Arthritis (Vancouver Criteria)
- Criteria for the Diagnosis of Psoriatic Arthritis of the CASPAR Investigators
- Criteria of Vasey and Espinoza for Psoriatic Arthritis
- Modified Criteria of McGonagle et al for the Diagnosis of Psoriatic Arthritis
- Criteria of Fournie et al for Psoriatic Arthritis
- ILAR (International League of Assocations for Rheumatology) Criteria for Juvenile Psoriatic Arthritis
- Score of Wassenberg et al for Radiographic Changes in a Patient with Psoriatic Arthritis
- Classification of Disease Severity in Psoriatic Arthritis Based on Therapy and Disability
- Psoriatic Arthritis Response Criteria of Clegg et al (PsARC)
- Allergic Rhinitis Severity Score of Lunn et al
- Score for Allergic Rhinitis (SFAR) of Annesi-Maesano et al
- Allergic Rhinitis Severity Score of Berges-Gimeno et al
- Classification of Bousquet et al for Allergic Rhinitis
- Total Nasal Symptom Score (TNSS), Cough Score and Overall Symptom Score of Gawchik et al for a Patient with Allergic Rhinitis
- Indications for Referring a Patient with Allergic Rhinitis to a Specialist
- Model of Visser et al for Early Prediction of Outcome in Patients with Arthritis
- Synovialitis Score of Krenn et al for Grading Histologic Features of Chronic Synovitis
- Tool of Len et al for Identifying a Pediatric Patient with Chronic Arthropathy Who Should Be Referred to a Rheumatologist
- Prediction Rule of van der Helm-van Mil et al for Evaluating a Patient with a Recent Onset of Undifferentiated Arthritis
- Clinical Features of Parvovirus B19-Associated Arthropathy
- Relapsing Seronegative Symmetric Synovitis with Pitting Edema (RS3PE)
- Steroid Pseudorheumatism (Arthralgias and Myalgias Associated with Steroid Withdrawal)
- Arthritis Associated with Intestinal Bypass for Morbid Obesity (Intestinal Bypass Arthritis)
- Risk Factors of Gonzalez-Lopez et al for Subsequent Development of a Connective Tissue Disorder in a Patient with Palindromic Rheumatism
- Leprosy Presenting as an Autoimmune or Rheumatic Disorder
- Food-Induced Allergic Arthritis
- Dialysis-Related Amyloid Arthropathy (Beta2-Microglobulin Amyloid Arthropathy)
- Septic Focus Syndrome
- Early Persistent Inflammatory Synovitis Assessment (EPISA) Score of El Miedany et al
- Clinical Findings Associated with Viral Hepatitis C-Associated Arthropathy
- Differential Diagnosis of Recurrent or Relapsing Arthritis
- Celiac Disease Arthropathy (Arthritis of Celiac Disease)
- Evaluation of the Immune Status in a Patient With Bacterial Meningitis or Invasive Bacterial Infection
- Clinical Features of the X-Linked Hyper-IgM Syndrome
- Clinical Features of the Wiskott-Aldrich Syndrome (WAS)
- Clinical Features of Hyper-IgE Syndrome (HIES, Job Syndrome)
- Clinical Features of TAP Deficiency Syndrome (Type 1 BLS)
- Clinical Features of Selective IgA Deficiency (IgAD)
- Drug-Induced IgA Deficiency
- Algorithm of Snowden et al for Evaluating a Patient with Rheumatoid Arthritis and a Gold-Induced Immunoglobulin Deficiency
- When to Screen a Patient for a Primary Antibody Deficiency
- When to Suspect Autosomal Recessive Agammaglobulinemia (ARA)
- Drug-Induced Hypogammaglobulinemia
- Transient Hypogammaglobulinemia of Infancy (THI)
- Common Variable Immunodeficiency (CVID)
- Clinical and Laboratory Features of Agammaglobulinemia
- Causes of Acquired Hypogammaglobulinemia
- Specific Antibody Deficiency (SAD) and Poor Response to Polysaccharide Vaccines
- Clinical Findings in an Infant with Omenn's Syndrome
- Clinical Features of X-Linked Severe Combined Immunodeficiency (SCID)
- Clinical Features of Severe Combined Immunodeficiency (SCID) Associated with Adenosine Deaminase (ADA) Deficiency
- Lymphocyte Phenotypes Associated with Various Combined Immunodeficiencies
- Clinical Features of ZAP70-Related Severe Combined Immunodeficiency (SCID)
- Monocytopenia Immunodeficiency Syndrome (MonoMAC) with Bone Marrow Failure
- The 10 Warning Signs for Primary Immunodeficiency in Children of the Jeffrey Modell Foundation Medical Advisory Board
- Warning Signs of Subbarayan et al for Primary Immunodeficiency Disease in Children
- Severe Combined Immunodeficiency (SCID) Associated with CD3 delta Deficiency Involving T Lymphocytes
- Predisposition to Infection Associated with Anticytokine Autoantibodies
- When to Suspect the Presence of an Anticytokine Autoantibody
- Score of Agarwal and Cunningham-Rundles for Management of a Patient with Hypogammaglobulinemia
- Solar Urticaria
- Aquagenic Urticaria and Aquagenic Pruritus
- Cholinergic Urticaria (Generalized Heat-Induced Urticaria)
- Dermographism (Dermatographism)
- Classification of Fukunaga et al for Cholinergic Urticaria Based on Autologous Skin Testing
- Separating a Significant Cold Agglutinin from a Laboratory Annoyance
- Autoimmune Hemolytic Disease Associated with a Mature Teratoma or Other Ovarian Tumor
- Paroxysmal Cold Hemoglobinuria (PCH, Donath Landsteiner Antibody-Related Hemolysis)
- Indications for a Patient to Carry an Epinephrine (Adrenaline) Auto-Injector
- Grades of Laxenaire for the Severity of an Anaphylactoid Reaction
- Grading System of Brown for a Generalized Hypersensitivity Reaction
- Risk Factors of Brown for Hypoxia in a Patient with a Generalized Hypersensitivity Reaction
- Risk Factors of Brown for Hypotension in a Patient with a Generalized Hypersensitivity Reaction
- Impact of Beta-Adrenergic Blocking Agents on a Patient with Anaphylaxis
- Criteria of Sampson et al for Anaphylaxis
- Grading Scheme of Ring and Messmer for Anaphylactic Symptoms
- Nitritoid Reaction Following Gold Salt (Sodium Aurothiomalate) Therapy
- Biphasic Anaphylactic Event
- Serum Tryptase Activity
- Classification of Montgomery et al for an Allergic Reaction to Isosulfan Blue Dye During Lymphatic Mapping
- Cytokine Release Syndrome (CRS)
- Clinical Features Associated with Interleukin-6 (IL-6, Interleukin-6 Syndrome)
- Clinical Features of the Jarisch-Herxheimer Reaction
- Infections Associated with a Jarisch-Herxheimer Reaction
- Hereditary Defects in the Interferon-gamma and Interleukin-12 Pathway (Hereditary Susceptibility to Mycobacteria and Intracellular Pathogens)
- Clinical Features of a Systemic Allergic Contact Dermatitis Reaction
- Systemic Allergic Contact Dermatitis with a Bathing Trunk Distribution (Baboon Syndrome)
- Grading Scale of Williams et al for Uroshiol Contact Dermatitis Following Exposure to Poison Ivy or Poison Oak
- Clinical Features of Metal Sensitivity in a Patient with an Orthopedic Implant
- Clinical Features of Mercury Sensitivity Associated with Dental Amalgam
- Clinical Features of Nickel Sensitivity
- Contact Allergic Reactions Following Exposure to Smoke from Burning Poison Ivy or Poison Oak
- Contact Allergic Dermatitis to Lacquer (Sap of the Rhus Tree)
- Systemic Allergic Dermatitis Following Oral Intake of Urushiol from the Rhus Tree as an Herbal Medicine
- Contact Allergic Dermatitis to Mango
- Contact Allergic Dermatitis to the Fruit of the Ginkgo Tree
- Contact Allergy to Polyvinylpyrrolidone, Including Povidone-Iodine
- Allergic Contact Sensitivity to Fiberglass (Fiberglass Dermatitis)
- Oral Allergy Syndrome (OAS, Mucosal Contact Urticaria, Food Contact Hypersensitivity Syndrome)
- Hypersensitivity Reaction to a Ventriculoperitoneal Shunt
- Phytodermatitis Associated with Metopium toxiferum (Poison Wood, Poison Bark)
- Phytodermatitis Associated with Parthenium Species
- Kimura's Disease
- Types of Brouet et al for Cryoglobulins
- Clinical Findings in a Patient with Cryoglobulinemia
- Reasons for Failure to Detect a Cryoglobulin
- Clinical Findings in a Patient with Cryofibrinogen
- Criteria for Essential Cryoglobulinemic Vasculitis from the International Consensus Conference on the Nomenclature of Systemic Vasculitis (Chapel Hill Conference)
- Cryocrit
- Criteria of Roccatello et al for Response to Therapy for a Patient with Cryoglobulinemia
- Cryogelation Associated with Waldenstrom's Macroglobulinemia
- Clinical Features of Goodpasture's Disease
- Differential Diagnosis of Goodpasture's Syndrome
- Risk Factors for Exacerbation of Goodpasture's Disease
- Prognostic Factors of Levy et al for a Patient with Goodpasture's Disease
- Clinical Features of the Autoimmune Lymphoproliferative Syndrome (ALPS)
- Lofgren's Syndrome
- Clinical Features Associated with an Acute vs Chronic Course in Systemic Sarcoidosis
- Indications for Oral Corticosteroid Therapy in a Patient with Sarcoidosis
- Criteria of Mana for Disease Activity in Sarcoidosis
- Sarcoidosis Following Therapy with a Tumor Necrosis Factor (TNF) alpha Blocking Agent
- Method of Judson for Assessing the Clinical Severity of Sarcoidosis
- Acute Sarcoid Myositis (Acute Sarcoid Myopathy)
- Blau Syndrome and NOD2 Mutations (Granulomatous Dermatitis, Uveitis and Arthritis)
- Prognostic Factors of Neville et al for a Patient with Sarcoidosis
- Reactivation of Sarcoidosis in a Patient Being Treated with Interferon
- Late-Onset Sarcoidosis
- Sarcoidosis Severity Scores of Wasfi et al
- Clinical Severity Score of Gedalia et al for a Pediatric Patient with Sarcoidosis
- Response Criteria of Gedalia et al in a Pediatric Patient with Sarcoidosis Treated with Methotrexate
- Causes of a Misleading Allergen Skin Test
- Skin Index of Ueno et al in Allergen Testing
- Clinical Findings in Retroperitoneal Fibrosis
- Causes of Retroperitoneal Fibrosis
- Algorithm of Vaglio et al for the Management of a Patient with Retroperitoneal Fibrosis
- Criteria of the Japanese Adult Still's Disease Research Committee for Adult Still's Disease (Yamaguchi Criteria)
- Criteria of Fautrel et al for Adult Onset Still's Disease (AOSD)
- Criteria of Cush et al for Adult Onset Still's Disease
- Clinical Findings of Efthimiou et al for Adult Onset Still's Disease
- Risk Factors of Kong et al for Relapse in a Patient with Adult-Onset Still's Disease
- Response Criteria of Fautrel et al to Therapy for Adult Still's Disease
- Criteria of the Pediatric Rheumatology International Trials Organization (PRINTO) for Improvement in Juvenile Arthritis
- ILAR (International League of Associations for Rheumatology) Criteria for Idiopathic Juvenile Oligoarthritis
- ILAR (International League of Associations for Rheumatology) Criteria for Idiopathic Juvenile Polyarthritis
- ILAR (International League of Associations for Rheumatology) Criteria for Idiopathic Juvenile Systemic Arthritis
- ILAR (International League of Associations for Rheumatology) Criteria for "Other" Juvenile Arthritis
- The Pediatric Escola Paulista de Medicina Range of Motion (EPM-ROM) Scale for Juvenile Rheumatoid Arthritis
- American Rheumatism Association (ARA) Criteria for Juvenile Rheumatoid Arthritis
- Risk of Malignancy in a Patient with Juvenile Arthritis Treated with a Tumor Necrosis Factor (TNF) alpha Inhibitor
- Criteria of Wallace et al for Inactive Juvenile Idiopathic Arthritis (JIA)
- Predictors of Schneider et al for Poor Functional Outcome in a Patient with Systemic-Onset Juvenile Rheumatoid Arthritis (JRA)
- Criteria of Chamot et al for the SAPHO Syndrome
- Criteria of Alarcon-Segovia and Villareal for the Diagnosis of Mixed Connective Tissue Disease
- Criteria of Sharp for the Diagnosis of Mixed Connective Tissue Disease
- Criteria of Kasukawa et al for the Diagnosis of Mixed Connective Tissue Disease
- Discriminant Function of Ishikawa et al for Distinguishing Mixed Connective Tissue Disease from Progressive Systemic Sclerosis
- Diagnostic Criteria of Scully et al for Familial Mediterranean Fever
- Clinical Features of the Hyper-IgD Syndrome
- Clinical Features of the TNF-Receptor Associated Periodic Syndrome (TRAP, Familial Hibernian Fever)
- Criteria of Livneh et al for Complete or Incomplete Attacks in a Patient with Familial Mediterranean Fever
- Criteria of Livneh et al for the Diagnosis of Familial Mediterranean Fever
- Simplified Criteria of Livneh et al for the Diagnosis of Familial Mediterranean Fever
- Clinical Features of the Familial Cold Autoinflammatory Syndrome (Familial Cold Urticaria)
- Clinical Score of Settin et al for Familial Mediterranean Fever (FMF)
- Indications for Using Colchicine in a Patient with Familial Mediterranean Fever
- Clinical Features of Muckle-Wells Syndrome
- Clinical Features of Chronic Infantile Neurological Cutaneous Articular Syndrome (CINCA Syndrome, NOMID)
- Criteria for Microscopic Polyangiitis from the International Consensus Conference on the Nomenclature of Systemic Vasculitis (Chapel Hill Conference)
- Differentiating Microscopic Polyangiitis from Polyarteritis Nodosa (PAN)
- Clinical Features of Microscopic Polyangiitis
- Criteria of Moore for Isolated Angiitis of the Central Nervous System
- High Risk Profile of Benseler et al for a Child with Primary Central Nervous System Vasculitis
- Criteria of Calabrese and Mallek for Primary Angiitis of the Central Nervous System (PACNS)
- Benign Angiopathy of the Central Nervous System (Benign Angiitis of the Central Nervous System, BACNS)
- Differential Diagnosis of Primary Angiitis of the Central Nervous System (PACNS)
- Clinical Features of Cogan Syndrome
- Risk of Exposure to Cockroach Allergens
- Reducing Exposure to Dust Mite Allergens
- Pancake Syndrome (Oral Mite Anaphylaxis)
- Diseases That May Be Seen in a Patient with an Inherited Complement Deficiency
- Body Fluid to Serum CH50 Ratio
- Screening for a Complement Deficiency Using the CH50 and AH50
- Criteria of Grotz et al for the Hypocomplementemic Urticarial Vasculitis Syndrome (HUVS, Anti-C1q Syndrome)
- Clinical Features of Hereditary C3 Deficiency
- SLE and Other Clinical Features of a Homozygous Deficiency in a Component of the Classical Complement Pathway
- Risk for Neisseria Infections in a Patient Treated with Eculizumab
- Preliminary Criteria of Mosca et al for Undifferentiated Connective Tissue Disease
- Clinical and Laboratory Findings in a Patient with Undifferentiated Connective Tissue Disease
- Findings in a Patient with Apparent Undifferentiated Connective Tissue Disease Who May Progress to Systemic Lupus Erythematosus (SLE)
- Allergy to Ethylene Oxide
- Clinical Clues of Naschitz for Occult Neoplasia in a Patient Presenting with a Rheumatic Disorder
- Palmar Fasciitis and Polyarthritis Syndrome (PFPAS)
- Paraneoplastic Autoimmune Multiorgan Syndrome (PAMS)
- Minimum Workup of Mourad et al to Qualify for Fever of Unknown Origin
- Algorithm of Mourad et al for Evaluating a Patient with Fever of Unknown Origin (FUO)
- Conditions Associated with Fever of Unknown Origin (FUO)
- Drugs That Can Cause Fever of Unknown Origin
- Diagnostic Approach of Wagner et al to Identify Large Vessel Vasculitis in a Patient with Fever of Unknown Origin (FUO)
- Criteria for the Diagnosis of a Fever of Unknown Origin (FUO)
- Clinical Features of Serum Sickness
- Drugs That Can Cause a Serum Sickness Like Reaction (SSLR)
- Features of a Serum Sickness-Like Reaction
- Classification of Gell and Coombs for Hypersensitivity Reactions
- Contraindications to a Corticosteroid Injection
- “Steroid Flare” Following an Intraarticular Injection of a Corticosteroid
- Clinical Features of Chronic Recurrent Multifocal Osteomyelitis
- Clinical Features of Chronic Nonbacterial Osteomyelitis (CNO)
- Response to Therapy by a Patient with Chronic Recurrent Multifocal Osteomyelitis
- Criteria of Masaki et al for IgG4-Positive Multi-Organ Lymphoproliferative Syndrome
- Criteria of Yamamoto et al for Mikulicz's Disease with Involvement of Lacrimal and Salivary Glands
- FDG PET-CT Scan for Evaluation of the Patient for IgG4-Related Plasmacytic Syndrome
- Reducing Exposure to Pet Dander
- Christmas Tree Syndrome (Christmas Tree Allergy)
- Recommendations of Kurlandsky et al to Reduce Allergen Exposure Associated with a Coniferous Tree or Other Plant Decorations
- Airborne Contact Dermatitis (ABCD)
- Criteria of Umeki for Eosinophilic Pneumonia
- Distinguishing Acute and Chronic Eosinophilic Pneumonia
- Risk Factors of Scranton et al for a Biphasic Reaction Associated with Allergen Immunotherapy
- Indications of Li et al for Allergen Immunotherapy in a Patient with Allergic Rhinitis and/or Allergic Asthma
- Contraindications to Performing a Radioallergosorbent Test (RAST) to Detect Specific IgE Antibody
- CAP System Scoring Scheme for a Radioallergosorbent Test (RAST)
- Indications to Performing a Radioallergosorbent Test (RAST) to Detect Specific IgE Antibody
- Clinical Features of Sclerosing Mediastinitis
- Causes of the Abnormal Immunological Response in Sclerosing Mediastinitis
- Prognostic Factors for a Patient with Sclerosing Mediastinitis
- Clinical and Laboratory Features of the Antisynthetase Syndrome
- Mechanic's Hands
- Daily Urticaria Activity Score (UAS)
- Using the Urticaria Activity Score (UAS) to Measure Response to Therapy for Chronic Urticaria
- Symptom Score of Mlynek et al for a Patient with Chronic Urticaria
- Scoring System of Kaplan et al for Urticaria Severity
- Clinical and Laboratory Features of Chronic Autoimmune Urticaria
- Autologous Serum Skin Test (ASST) in Chronic Idiopathic Urticaria
- Criteria of Rodriguez for an Autoimmune Disorder
- Moyamoya Syndrome in a Patient with Systemic Lupus Erythematosus (SLE)
- Score of Crowson et al for Predicting the Risk of a Serious Infection in a Patient with Rheumatoid Arthritis (RA)
- Additional Clinical and Laboratory Findings in Behcet’s Disease
- Prognostic Score of Wingard et al for a Patient with Chronic Graft-versus-Host Disease After Bone Marrow Transplantation
- Chronic Graft-versus-Host Disease (GVHD) Score of Lee et al.
- Clinical Score of Jacobsohn et al for Grading Chronic Graft-versus-Host Disease (GVHD)
- Criteria of Jacobsohn et al for Therapeutic Response in a Patient Being Treated for Chronic Graft-versus-Host Disease (GVHD)
- Chronic GVHD Risk Score of Arora et al
- Revised Classification Score of Cornec et al for Primary Sjogren's Syndrome (SS)
- Ultrasound Inhomogeneity Score of Milic et al for a Patient with Sjogren's Syndrome
- Paraneoplastic Scleroderma (Sclerodermiform Paraneoplastic Syndrome)
- Disease Severity Score of La Torre et al for Juvenile Systemic Sclerosis
- Predisposition to Fungal Infections Associated with Hereditary CARD9 Deficiency
- Hereditary Conditions Associated with Impaired Interleukin-17 (IL-17) Function and Mucocutaneous Candidiasis
- Definition of Micek et al for Immunosuppression
- Tulip Fingers
- Revised Criteria of Oliveira et al for Autoimmune Lymphoproliferative Syndrome (ALPS)
- Nomenclature of Oliveira et al for Autoimmune Lymphoproliferative Syndrome (ALPS)
- Recommended Initial Evaluation of a Patient with Sarcoidosis from the ATS/ERS/WASOG Statement
- Clinical Features of Cellucci et al for a Child with Primary Angiitis of the Central Nervous System
- Laboratory Findings of Cunha et al Associated with Tumor-Related Tumor Necrosis Factor
- Naproxen Test (Naprosyn Test, NSAID Test) for Fever of Unknown Origin (FUO) Associated with an Underlying Cancer
- Aseptic Abscess Syndrome (AAS)
- Conditions Associated with the Splendore-Hoeppli Phenomenon
- Histologic Features of the Splendore-Hoeppli Phenomenon
- Criteria of Damiani and Levine for the Diagnosis of Relapsing Polychondritis
- 1997 ACR Update in the Criteria for the Diagnosis of Systemic Lupus Erythematosus
- Clinical and Laboratory Findings of Lupus Enteritis
- Intestinal Ischemia or Infarction in Rheumatoid Arthritis
- Algorithm of Dammacco and Sansonno for Managing a Patient with HCV-Related Cryoglobulinemia
- Predictors of van Dartel et al for Serious Infection in a Patient with Rheumatoid Arthritis Treated with Anti-Tumor Necrosis Factor (TNF alpha) Therapy
- Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) (German)
- Chronic Fatigue Syndrome Severity Score of Baraniuk et al
- Criteria of the Institute of Medicine (IOM) for Myalgic Encephalitis/Chronic Fatigue Syndrome (ME/CFS, Systemic Exertional Intolerance Disease, SEID)
- Risk Factors of Gustafsson et al for a First Cardiovascular Event in a Patient with Systemic Lupus Erythematosus
- Risk Factors of Martinez-Martinez et al for Mortality in a Patient with Systemic Lupus Erythematosus (SLE) and Diffuse Alveolar Hemorrhage (DAH)
- Rheumatoid Arthritis Observation of Biologic Therapy (RABBIT) Risk Scores for Serious Infection
- Rheumatoid Nodulosis
- Accelerated Nodulosis and Vasculitis Associated with Methotrexate Therapy in a Patient with Rheumatoid Arthritis
- Simplified Model of de Punder et al for Predicting Joint Damage Progression in a Patient with Rheumatoid Arthitis
- Extended Model of de Punder et al for Predicting Joint Damage Progression in a Patient with Rheumatoid Arthitis
- Subglottic Stenosis and Other Manifestations of Wegener?s Granulomatosis (Granulomatosis with Polyangiitis) Involving the Laryngotracheobronchial Tree
- Carotidynia in Takayasu Arteritis
- Sjogren's Syndrome Associated with Sarcoidosis
- Pseudo-Asthma Secondary to Relapsing Polychondritis
- Criteria of Michet et al for the Diagnosis of Relapsing Polychondritis
- Prognostic Factors of Michet et al for a Young Adult with Relapsing Polychondritis
- Histologic Findings in Relapsing Polychondritis
- Susac Syndrome
- Lymphocytopenia Associated with a Lymphatic Malformation
- Cytokine Storm Associated with TGN1412 (Anti-CD28 Monoclonal Antibody)
- Indications of Shohat and Halpern for Evaluating a Patient for Familial Mediterranean Fever
- Phenotypes of Familial Mediterranean Fever (FMF)
- Klassifikationskriterien für die rheumatoide Arthritis der American Rheumatism Association 1987 (German)
- Klassifikationskriterien für die rheumatoide Arthritis der American College of Rheumatology (ACR)/European League Against Rheumatism (EULAR) 2010 (German)
- Kriterien der kompletten Remission für die rheumatoide Arthritis der American Rheumatism Association 1981 (German)
- Risk Factors for Acute Myocardial Infarction in a Patient with Systemic Lupus Erythematosus
- Revised Cutaneous Lupus Erythematosus Disease Area and Severity Index (RCLASI): Skin Lesions Activity
- Revised Cutaneous Lupus Erythematosus Disease Area and Severity Index (RCLASI): Mucous Membrane Lesion Activity
- Revised Cutaneous Lupus Erythematosus Disease Area and Severity Index (RCLASI): Alopecia Activity
- Revised Cutaneous Lupus Erythematosus Disease Area and Severity Index (RCLASI): Skin Lesion Damage
- Revised Cutaneous Lupus Erythematosus Disease Area and Severity Index (RCLASI): Alopecia Damage
- Revised Cutaneous Lupus Erythematosus Disease Area and Severity Index (RCLASI): Total Activity and Damage Scores
- Clues to Large Granular Lymphocytic Leukemia as the Cause of Rheumatoid Arthritis
- Scoring Method of Zayat et al for Bone Erosions in Rheumatoid Arthritis Using Ultrasonography
- Flares in Rheumatoid Arthritis (RA)
- Overall Status of Rheumatoid Arthritis (OSRA) of Symmons et al
- Tendon Disorders in Rheumatoid Arthritis
- Classification of Klauser et al for Wrist Tenosynovitis in Rheumatoid Arthritis Using Ultrasonography
- Scoring Fatty Lesions and Erosions Involving the Sacroiliac Joints (SIJ) on MRI in a Patient with Axial Spondyloarthritis
- Screening Criteria from the Dublin Uveitis Evaluation Tool (DUET) for Spondyloarthritis and Inflammatory Backache
- Risk Factors of Maurer et al for Worsening of Skin Fibrosis in a Patient with Diffuse Cutaneous Systemic Sclerosis (dcSSc)
- Immunodeficiency Associated with Thymoma (Good's Syndrome)
- WHIM Syndrome (Warts, Hypogammaglobulinemia, Infection, Myelokathexis)
- Osteolytic Bone Lesions in Osseous Sarcoidosis Mimicking Metastatic Carcinoma
- MRI Tenosynovitis Score of Lambot et al in a Patient with Juvenile Idiopathic Arthritis
- Risk Factors of Guillaume et al for Complications in a Patient Presenting with Oligoarticular Juvenile Rheumatoid Arthritis (JRA)
- Classification of Dale et al for Radiographic Changes in the Knee for a Patient with Juvenile Rheumatoid Arthritis (JRA)
- Eurofever Clinical Criteria for TRAPS (TNF-Receptor Associated Periodic Syndrome)
- Eurofever Clinical Criteria for CAPS (Cryopyrin-Associated Periodic Syndrome)
- Eurofever Clinical Criteria for MKD (Mevalonate Kinase Deficiency, Hyper-IgD Syndrome)
- Eurofever Clinical Criteria for FMF (Familial Mediterranean Fever)
- Criteria of Yalcinkaya et al for the Diagnosis of Familial Mediterranean Fever in a Child
- Predictors of Legge et al for Progression of Organ Damage in a Patient with Systemic Lupus Erythematosus (SLE)
- Familial Chilblain Lupus (FCL)
- Elderly Onset Rheumatoid Arthritis (EORA, Late Onset RA) versus Younger-Onset Rheumatoid Arthritis (YORA)
- Risk Factors of Salmon et al for Serious Infection in a Patient with Rheumatoid Arthritis Treated with Abatacept (Orencia)
- Criteria of Grossman et al for Diagnosis of Giant Cell Arteritis (Temporal Arteritis) When the Temporal Artery Biopsy (TAB) Is Negative
- PEDBD Classification of Kone-Paut et al for Pediatric Behcet’s Disease
- Sclerotic-Type (Scleroderma-Like) Chronic Graft versus Host Disease (GVHD) Following Allogeneic Hematopoietic Stem Cell Transplant (HSCT)
- National Institutes of Health Criteria for Clinical Trials in Chronic Graft-versus-Host Disease (GVHD): Skin Involvement
- National Institutes of Health Criteria for Clinical Trials in Chronic Graft-versus-Host Disease (GVHD): Mouth and Gastrointestinal Tract Involvement
- National Institutes of Health Criteria for Clinical Trials in Chronic Graft-versus-Host Disease (GVHD): Lung Involvement
- National Institutes of Health Criteria for Clinical Trials in Chronic Graft-versus-Host Disease (GVHD): Ocular (Eye) Involvement
- National Institutes of Health Criteria for Clinical Trials in Chronic Graft-versus-Host Disease (GVHD): Female Genital Tract Involvement
- National Institutes of Health Criteria for Clinical Trials in Chronic Graft-versus-Host Disease (GVHD): Liver (Hepatic) Involvement
- National Institutes of Health Criteria for Clinical Trials in Chronic Graft-versus-Host Disease (GVHD): Joint and Fascia Involvement
- National Institutes of Health Criteria for Clinical Trials in Chronic Graft-versus-Host Disease (GVHD): Other Site Involvement
- National Institutes of Health Criteria for Clinical Trials in Chronic Graft-versus-Host Disease (GVHD): Performance Score and Summary Status
- National Institutes of Health Criteria for Clinical Trials in Chronic Graft-versus-Host Disease (GVHD): Categories of Acute and Chronic GVHD
- National Institutes of Health Criteria for Clinical Trials in Chronic Graft-versus-Host Disease (GVHD): Global Score
- EULAR Primary Sjogren’s Syndrome Disease Activity (ESSDAI): Constitutional Subscore
- EULAR Primary Sjogren’s Syndrome Disease Activity (ESSDAI): Lymphadenopathy Subscore
- EULAR Primary Sjogren’s Syndrome Disease Activity (ESSDAI): Glandular Subscore
- EULAR Primary Sjogren’s Syndrome Disease Activity (ESSDAI): Articular Subscore
- EULAR Primary Sjogren’s Syndrome Disease Activity (ESSDAI): Cutaneous Subscore
- EULAR Primary Sjogren’s Syndrome Disease Activity (ESSDAI): Pulmonary Subscore
- EULAR Primary Sjogren’s Syndrome Disease Activity (ESSDAI): Renal Subscore
- EULAR Primary Sjogren’s Syndrome Disease Activity (ESSDAI): Muscle Subscore
- EULAR Primary Sjogren’s Syndrome Disease Activity (ESSDAI): Peripheral Nervous System (PNS) Subscore
- EULAR Primary Sjogren’s Syndrome Disease Activity (ESSDAI): Central Nervous System (CNS) Subscore
- EULAR Primary Sjogren’s Syndrome Disease Activity (ESSDAI): Hematological Subscore
- EULAR Primary Sjogren’s Syndrome Disease Activity (ESSDAI): Biological Subscore
- EULAR Primary Sjogren’s Syndrome Disease Activity (ESSDAI): Total Score
- EULAR Sjogren's Syndrome Patient Reported Index (ESSPRI)
- Simplified Version of the Ankylosing Spondylitis Disease Activity Score (SASDAS)
- Reactive Arthritis in a Patient with Giardiasis
- American College of Rheumatology (ACR) Composite Response Index for Systemic Sclerosis (CRISS): Failure to Improve
- American College of Rheumatology (ACR) Composite Response Index for Systemic Sclerosis (CRISS): Probability of Improvement
- Red Flags of Li et al for a Patient with Scleroderma
- Predictive Factors of Xu et al for Rapidly-Progressive Interstitial Lung Disease (ILD) in a Patient with Clinically Amyopathic Dermatomyositis (CADM)
- Ocular Myasthenia Gravis (OMG)
- Pediatric Myasthenia Gravis
- Preliminary Criteria of De Vita et al for the Diagnosis of Cryoglobulinemic Vasculitis
- Criteria of Ravelli et al for Macrophage Activation Syndrome (MAS) Complicating Systemic Juvenile Idiopathic Arthritis (JIA)
- Risk Factors of Guzman et al for Flares in a Patient with Juvenile Idiopathic Arthritis (JIA)
- Chronic Arthritis Score (CASco) of Cattalini et al for Evaluating a Child with Musculoskeletal Complaints
- International Severity Scoring System of Demirkaya et al for Familial Mediterranean Fever (FMF, ISSF)
- Diagnostic Criteria of Jansson et al for Nonbacterial Osteitis (NBO)
- Lupus Low Disease Activity State (LLDAS) of Franklyn et al for a Patient with SLE
- Classification Criteria of the American College of Rheumatology (ACR) and the European League Against Rheumatism (EULAR) for Primary Sjogren's Syndrome (SS)
- Prognostic Factors of Brito-Zeron et al for a Patient with Primary Sjogren's Syndrome
- Revised Criteria of Valentini et al for Activity of Systemic Sclerosis (Revised EUSTAR Activity Index)
- Dermatomyositis Skin Severity Index (DSSI) of Carroll et al
- STING-Associated Vasculopathy with Onset in Infancy (SAVI)
- Skin Lesions in Patients with IgG4-Related Disease
- Allergy to Alpha-Gal (Red Meat Allergy Syndrome)
- Time Course of an Immune Response to an Antigenic Stimulus (Primary and Secondary Immune Response)
- SLEDAI-2K Score for Systemic Lupus Erythematosus (SLE)
- Lupus Headache
- Lupus Tumidus (Lupus Erythematosus Tumidus)
- Extra-Articular Involvement and Complications of Rheumatoid Arthritis
- Leeds Enthesitis Index (LEI) of Healy and Helliwell
- Enthesitis Index of the Spondyloarthritis Research Consortium of Canada (SPARCC)
- ASAS Classification Criteria for Peripheral Spondyloarthritis
- Capillaroscopic Skin Ulcer Risk Index (CSURI) for a Patient with Systemic Sclerosis
- Significance of Skin Telangiectasia for a Patient with Systemic Sclerosis Based on the Study of Hurabielle et al
- Clinical Findings of McCann and Pain Associated with Severe Juvenile Dermatomyositis (JDM)
- Clinical Predictors of Wang et al for Prognosis in a Patient with Myasthenia Gravis
- Drug-Induced Exacerbation of Myasthenia Gravis (MG)
- Refractory Myasthenia Gravis (MG)
- Diagnostic Criteria of Sudulagunta et al for Myasthenia Gravis (MG)
- Clinical Features of Myasthenia Gravis Associated with Anti-MuSK (IgG4-Related MG)
- Transient Neonatal Myasthenia Gravis (TNMG)
- Eosinophilic Arthritis
- Idiopathic CD4 Lymphocytopenia (ICL, Pseudo-HIV Disease)
- Age-Related Immunodeficiency (Senile Immunodeficiency, Immune Senescence)
- Immunocompromising Conditions of Tande et al
- Autoimmune Paraneoplastic Syndromes in Patients with the Myelodysplastic Syndrome (MDS)
- Criteria of Vodovar et al for Drug Fever (DF)
- Cardiovascular Manifestations in IgG4-Related Disease
- Prognostic Factors of Shi et al for a Patient with Antisynthetase Autoantibodies
- Autoinflammatory Disease Damage Index (ADDI) of ter Haar et al
- Lupus Mesenteric Vasculitis
- Differential Diagnosis of an Elevated Serum Creatine Kinase (CK) in a Patient with Systemic Lupus Erythematosus (SLE)
- Pseudo-SLE Associated with Parvovirus B19 Infection
- Diffuse Alveolar Hemorrhage (DAH) in a Patient with Systemic Lupus Erythematosus (SLE)
- Intestinal Pseudo-Obstruction (IPO) in Systemic Lupus Erythematosus (SLE)
- Predictors of Lim et al for the Damage Trajectory of a Patient with Juvenile-Onset Systemic Lupus Erythematosus (SLE)
- Hyperviscosity Syndrome in Rheumatoid Arthritis (RA)
- Criteria of de Hair et al for Difficult-to-Treat Rheumatoid Arthritis (RA)
- Clinical and Laboratory Findings Associated with a Worse Prognosis for a Patient with Rheumatoid Arthritis (RA)
- EULAR/PReS Criteria for Childhood Vasculitides: Childhood Polyarteritis Nodosa (PAN)
- EULAR/PReS Criteria for Childhood Vasculitides: Description of Childhood Cutaneous Polyarteritis
- Markers of Kato et al for Relapse of Cutaneous Polyarteritis Nodosa
- EULAR/PReS Criteria for Childhood Vasculitides: Wegener's Granulomatosis (Granulomatosis with Polyangiitis)
- Risk Factors of Charlier et al for Major Infections in a Patient with Wegener's Granulomatosis
- Aortitis in a Patient with Giant Cell Arteritis (GCA)
- EULAR/PReS Criteria for Childhood Vasculitides: Henoch Schonlein Purpura
- 2008 Criteria of EULAR/PRINTO/PRES for Pediatric Henoch-Schonlein Purpura
- Indications for Admitting a Patient with Henoch-Schonlein Purpura (HSP) Into the Hospital
- EULAR/PReS Criteria for Childhood Vasculitides: Takayasu Arteritis
- Risk of Malignancy in a Patient with Intestinal Behcet's Disease
- EULAR/PReS Criteria for Childhood Vasculitides: Classification
- Combined Arteritis Damage Score (CARDS) of Nakagomi et al for Large Vessel Vasculitis
- Criteria of Poddubnyy et al for Referral of a Patient with Suspected Axial Spondyloarthritis to a Rheumatologist (ASAS Recommendations)
- Scleroderma Acrosclerosis
- Classification of Peterson et al for Morphea (Localized Scleroderma, Mayo Clinic Classification)
- Skin Thickness Progression Rate (STPR) of Domsic et al for a Patient with Diffuse Scleroderma
- Prediction Rule of Domsic et al for Two Year Mortality for a Patient with Early Diffuse Cutaneous Systemic Sclerosis
- 2013 ACR/EULAR Classification Criteria for Systemic Sclerosis
- Systemic Sclerosis and Systemic Lupus Erythematosus (SLE) Overlap Syndrome (Lupoderma)
- Juvenile Idiopathic Inflammatory Myopathy with Anti-HMGCR Autoantibodies
- Predictors of Mazzoli et al for Progression from Ocular to Generalized Myasthenia Gravis
- Fetal Acetylcholine Receptor (ACR) Inactivation Syndrome
- Myasthenia Gravis Status and Treatment Intensity (MGSTI)
- PURE-4 Scale of Audureau et al Psoriatic Arthritis Screening
- EULAR Criteria for Arthralgia at Risk for Rheumatoid Arthritis
- Clinical Prediction Rule of van de Stadt et al for Predicting Arthritis in a Seropositive Patient with Arthralgia
- Arthralgia or Arthritis Associated with Parasitic Disease
- HUPI Index of Castrejon et al for Evaluating a Patient with Early Arthritis
- ICF Syndrome (Immunodeficiency, Centromeric Instability, Facial Anomalies)
- Granulomatous Common Variable Immune Deficiency (CVID) Mimicking Sarcoidosis
- Differentiating Common Variable Immunodeficiency (CVID) from IgG Deficiency
- Allergic Contact Cheilitis
- Predictors of Vorselaars et al for Relapse of Sarcoidosis Following Discontinuation of Infliximab Therapy
- 10 Joint Juvenile Arthritis Disease Activity Score (JADAS-10) of Consolaro et al
- Disease Activity States of Consolaro et al for Nonsystemic Juvenile Idiopathic Arthritis Based on the 3-Item cJADAS10
- NLRP1-Associated Autoinflammation with Arthritis and Dyskeratosis (NAIAD)
- Chronic Atypical Neutrophilic Dermatosis with Lipodystrophy and Elevated Temperature (CANDLE) Syndrome
- Paraneoplastic Large Vessel Vasculitis with Aortitis
- Clinical Score of Jansson et al for Nonbacterial Osteitis (NBO)
- Criteria of Masaki et al for IgG4-Related Mikulicz's Disease
- Criteria of Kawano et al for IgG4-Related Kidney Disease
- Comprehensive Criteria for the Diagnosis (CCD) of Umehara et al for IgG4-Related Disease
- Organ Involvement in IgG4-Related Disease
- Differential Diagnosis of an Elevated Serum IgG4 Concentration
- Clinical Features of the Aicardi-Goutieres Syndrome
- Clinical and Pathologic Features of Eosinophilic Fasciitis (EF, Shulman Disease)
- Systemic Immune-Inflammation Index (SIII)
- Platelet-to-Lymphocyte Ratio (PLR)
- Neutrophil-to-Lymphocyte Ratio (NLR)
- EULAR Criteria for Arthralgia That Is Suspicious for Progression to Rheumatoid Arthritis (RA)
- Double and Triple Seronegative Rheumatoid Arthritis
- Prognostic Factors of Fan et al for a Pediatric Patient with Takayasu's Arteritis
- Risk Factors of Gordon et al for Scleroderma Renal Crisis That Can Be Identified at the Time of Scleroderma Diagnosis
- Diagnostic Criteria for Nakajo-Nishimura Syndrome (NNS)
- Joint Contractures, Muscular Atrophy, Microcytic Anemia and Panniculitis-Associated Lipodystrophy (JMP Syndrome)
- Japanese Autoinflammatory Syndrome with Lipodystrophy (JASL)
- Lupus Mimics/Mimickers
- 2019 EULAR/ACR Classification Criteria for Systemic Lupus Erythematosus
- Rheumatoid Arthritis Refractory to Therapy
- Clinical Arthritis Rule (CARE) of ten Brinck for Recognition of Early Inflammatory Arthritis
- Japanese Vasculitis Activity Score (JVAS) for MPO-ANCA Positive Microscopic Polyangiitis with Renal Involvement
- Risk Factors of Yamaguchi for Severe Infection in a Patient with ANCA-Associated Vasculitis Receiving Immunosuppressive Therapy
- Grading System of Lee et al for the Cytokine Release Syndrome (CRS)
- Predictive Factors of Yang et al for Macrophage Activation Syndrome (MAS) in a Patient with Adult-Onset Still's Disease (AOSD)
- Risk Factors for Candida Pericarditis
- Systemic Lupus Erythematosus Disease Activity Score (SLE-DAS) of Jesus et al
- Criteria of Brunner et al for a Flare in Childhood-Onset Systemic Lupus Erythematosus (SLE): SLEDAI-Based Flare Score
- Criteria of Brunner et al for a Flare in Childhood-Onset Systemic Lupus Erythematosus (SLE): BILAG-Based Flare Score
- Model of Elman et al for the Diagnosis of Discoid Lupus Erythematosus (DLE)
- Criteria of Aletaha et al for Disease Activity in Rheumatoid Arthritis
- Risk Factors of Hocevar et al for a Severe Cranial Ischemic Event Associated with Giant Cell Arteritis
- Risk Factors of Salvarani et al for Cranial Ischemic Events (CIE) Associated with Giant Cell Arteritis
- Clinical Findings of van der Geest in the Diagnosis of Giant Cell Arteritis (GCA)
- Indian Takayasu's Arteritis Activity Score (ITAS2010 and ITAS.A)
- Score of Davatchi et al for the Diagnosis of Behcet's Disease
- Endothelial Activation and Stress Index (EASIX) of Luft et al in Acute Graft-versus-Host Disease (GVHD)
- Relapsing Polychondritis Damage Index (RPDAM) of Mertz et al
- Relapsing Polychondritis Disease Activity Index (RPDAI) of Arnaud et al
- ASAS Classification Criteria for Axial Spondyloarthritis: Sets 1 and 2
- Glasgow Ultrasound Enthesitis Scoring System (GUESS) for the Lower Extremities
- Scleroderma Clinical Trials Consortium Damage Index (SCTC-DI)
- Linear Scleroderma (Morphea) with Facial En Coup Sabre (ECS)
- Angioedema Associated with Angiotensin Converting Enzyme Inhibition (ACEI)
- Scurvy Mimicking a Rheumatic Disorder
- Differential Diagnosis of Acute Monoarthritis
- Indications to Refer a Patient with Acute Monoarthritis
- Criteria of Davila et al for Severe Cytokine Release Syndrome (CRS)
- Rituximab-Associated Flare of Mixed Cryoglobulinemia Vasculitis
- IgG4-Related Disease (IgG4-RD) Responder Index of Carruthers et al
- Celiac Disease Co-Existing with Systemic Lupus Erythematosus
- Predictors of Cho et al for a Flare in a Stable Asian Patient with Systemic Lupus Erythematosus (SLE)
- Criteria of Polachek et al for Low Disease Activity (LDA) in a Patient with Systemic Lupus Erythematosus (SLE)
- Criteria of Zen et al for Minimal Disease Activity (MDA) in a Patient with Systemic Lupus Erythematosus (SLE)
- Responder Index of Furie et al for a Patient with Systemic Lupus Erythematosus (SLE)
- Lupus Hepatitis
- Refractory Ascites in a Patient with Systemic Lupus Erythematosus (SLE)
- Risk Factors of Huang et al for Seizures in a Patient with Systemic Lupus Erythematosus (SLE)
- Oral Mucosal Lupus Erythematosus
- Definition of Remission in Systemic Lupus Erythematosus (DORIS)
- Lupus Myelitis
- Systemic Lupus Erythematosus (SLE) Associated Acute Pancreatitis
- Lupus Esophagus
- Systemic Lupus Erythematosus (SLE) Associated Sjogren's Syndrome
- EULAR Definition of Difficult-to-Treat Rheumatoid Arthritis
- Matrix of Vanier et al for Prediction of Rapid Radiographic Progression of Early Rheumatoid Arthritis (RA)
- Manifestations of Henoch-Schonlein Purpura in the Central Nervous System
- Angiographic Classification of Numano et al for Takayasu Arteritis
- Classification of Goel et al for Angiographic Distribution of Takayasu Arteritis
- Distal Renal Tubular Acidosis Associated with Sjogren's Syndrome
- ANCA-Associated Vasculitis with Bronchiectasis
- Vasculitis Associated with Myelodysplastic Syndrome or Chronic Myelomonocytic Leukemia (CMML)
- Risk Factors of Michelena et al for Renal Impairment in Axial Spondyloarthritis
- Gastrointestinal Involvement in Systemic Sclerosis (Scleroderma)
- Risk Factors of Mihai et al for Gangrene in a Patient with Systemic Sclerosis
- Systemic Sclerosis-Related Myocarditis
- Hand Morbidities Associated with Systemic Sclerosis
- Spanish Scleroderma Risk Score (RESCLESCORE) of Rubio-Rivas et al
- Predictors of Panopoulos et al for Mortality in a Patient with Systemic Sclerosis
- Prediction Rule of van den Hombergh et al for Diffuse Cutaneous Systemic Sclerosis
- Predictors of Scussel-Lonzetti et al for Mortality Due to Systemic Sclerosis
- Prediction Rule of Domsic et al for 5-Year Mortality Rate for a Patient with Early Diffuse Cutaneous Systemic Sclerosis
- Model of Beretta et al for 5-Year Mortality for a Patient with Systemic Sclerosis
- Polymyositis with Mitochondrial Pathology (PM-Mito)
- Poor Prognostic Factors (PPF) in Psoriatic Arthritis and Response to Abatacept Therapy
- Loss of Immune Memory (Immune Amnesia) Following an Acute Measles Infection
- Congenital Sideroblastic Anemia, B-Cell Immunodeficiency, Periodic Fevers and Developmental Delay (SIFD) Associated with Mutations in TRNT1
- Opioid-Related Immunosuppression
- T-Cell Exhaustion
- LRBA Deficiency
- Delayed Pressure Urticaria (DPU)
- Therapy of Cold Agglutinin Disease with Sutimlimab
- University of Pennsylvania (Penn) Cytokine Release Syndrome (CRS) Grading System
- Muscular Sarcoidosis
- Algorithm of Bilgin et al for Distinguishing Adult-Onset Still's Disease (AOSD) from Other Causes of Fever of Unknown Origin (FUO)
- MS Score of Minoia et al for Macrophage Activiation Syndrome (MAS) in Systemic Juvenile Idiopathic Arthritis (sJIA)
- Systemic Manifestation Score (SMS) of Saccomanno et al for a Patient with Systemic Juvenile Idiopathic Arthritis (sJIA)
- Predictors of Saccomanno et al for Response to Anakinra by a Patient with Systemic Juvenile Idiopathic Arthritis (sJIA)
- Clinical Features of the VEXAS Autoinflammatory Syndrome Associated with Somatic Mutations in UBA1
- Modified Score of Pras et al for Severity of Familial Mediterranean Fever (FMF) in Children
- Score of Pras et al for Severity of Familial Mediterranean Fever (FMF)
- SS2 Score of Mor et al for the Clinical Severity of Familial Mediterranean Fever (FMF)
- Auto-Inflammatory Diseases Activity Index (AIDAI) Diary: Daily Record for a Patient with Familial Mediterranean Fever (FMF)
- Auto-Inflammatory Diseases Activity Index (AIDAI) Diary: Daily Record for a Patient with Mevalonate Kinase Deficiency (MKD)
- Auto-Inflammatory Diseases Activity Index (AIDAI) Diary: Daily Record for a Patient with Tumor Necrosis Factor-1 Associated Periodic Syndrome (TRAPS)
- Auto-Inflammatory Diseases Activity Index (AIDAI) Diary: Daily Record for a Patient with Cryopyrin-Associated Periodic Syndrome (CAPS)
- Misdiagnosis of Antisynthetase Syndrome (Anti-Jo-1 Syndrome) as Rheumatoid Arthritis
- Diagnostic Criteria of Pinal-Fernandez et al al for Eosinophilic Fasciitis (EF, Shulman Disease)
- Lymphocyte-to-Monocyte Ratio
- Neutrophil-to-Platelet Ratio (NPR)
- Systemic Inflammation/Inflammatory Response Index (SIRI)
- The World Allergy Organization Subcutaneous Immunotherapy Systemic Reaction Grading System
- Subclinical Rejection (SCR, Subclinical Acute Rejection)
- Elevated Serum Lactate in a Patient with Chronic Fatigue Syndrome
- Pediatric Systemic Lupus Erythematosus (SLE) Associated with Constitutional Mismatch Repair Deficiency (CMMRD)
- Criteria of Lambers et al for Incomplete Systemic Lupus Erythematosus (SLE)
- Risk Factors of Curtis et al for Gastrointestinal Perforation in a Patient with Rheumatoid Arthritis
- Predictors of Syngle et al for Autonomic Neuropathy in a Patient with Rheumatoid Arthritis
- Systemic Sclerosis-Mixed Connective Tissue Disease (SSc-MCTD)
- Systemic Sclerosis Overlap Syndromes
- Drug-Induced Arthritis and Arthralgia
- Immune Deficiency and Dysregulation Activity (IDDA) Score of Tesch et al: Manifestation Grades
- Immune Deficiency and Dysregulation Activity (IDDA) Score of Tesch et al: Additional Findings
- Immune Deficiency and Dysregulation Activity (IDDA) Score of Tesch et al: Final Score Determination
- Clinical Findings That May Be Clues to a Primary Immunodeficiency
- ESID/PAGID 1999 Criteria for Common Variable Immunodeficiency Disorder (CVID)
- ESID 2014 Criteria for Common Variable Immunodeficiency Disorder (CVID)
- Differential Diagnosis of a Patient with Hypopigmentation and Primary Immunodeficiency
- Vici Syndrome (VICIS)
- Diagnostic Criteria of Ameratunga et al for Common Variable Immune Deficiency (CVID)
- Interleukin 1 Receptor Associated Kinase 4 (IRAK-4) Deficiency
- X-Linked Agammaglobulinemia (XLA)
- Griscelli Syndrome
- Immunodeficiency Associated with an IgG Subclass Deficiency
- MYD88 Deficiency
- Immunodeficiency Associated with LAMTOR2 (p14) Deficiency
- IKBKG and NFKBIA Deficiencies
- Photoallergic Contact Dermatitis (PACD) Score of Cazzaniga et al
- Criteria of Kahn and Appleboom for Mixed Connective Tissue Disease (MCTD)
- Clinical and Laboratory Findings of John et al for Mixed Connective Tissue Disease (MCTD)
- Refractory Familial Mediterranean Fever (FMF)
- Prognostic Factors of Tang et al for Microscopic Polyangiitis (mPA) with Diffuse Alveolar Hemorrhage (DAH)
- Hiker's Feet in Anti-Synthetase Syndrome
- Criteria of Shoenfeld and Agmon-Levin for Autoimmune/Inflammatory Syndrome Induced Adjuvants (ASIA)
- Neurologic Severity Scale of Adang et al for Aicardi Goutieres Syndrome (AGS Scale)
- SLEDAI 2K glucocorticoid index
- Infections That Mimic Rheumatoid Arthritis
- General Synovitis Score (GSS) and Immunologic Synovitis Score (ISS) for Evaluating a Patient with Rheumatoid Arthritis (RA)
- 2022 ACR/EULAR Classification Criteria for Eosinophilic Granulomatosis with Polyangiitis (EGPA)
- 2022 ACR/EULAR Classification Criteria for Granulomatosis with Polyangiitis (GPA)
- Polymyalgia Rheumatica Activity Score (PMR-AS)
- Score of Nagamori et al for Predicting Severe Gastrointestinal Disease Due to Henoch-Schonlein Purpura
- Prognostic Factors of Sugiyama et al for Interstitial Lung Disease (ILD) in a Patient with Polymyositis or Dermatomyositis
- Autoimmune Findings as a Warning Sign of Primary Immunodeficiency in a Pediatric Patient
- Pulmonary Complications Associated with Primary Immunodeficiency Syndromes
- Neonatal Lymphopenia and Severe Combined Immunodeficiency (SCID)
- PSTPIP1-Associated Myeloid-Related Proteinemia Inflammatory (PAMI) Syndrome
- 2022 ACR/EULAR Classification Criteria for Microscopic Polyangiitis (MPA)
- Advanced Lung Cancer Inflammation Index (ALI)
- Gustave Roussy Immune Score (GRIm-Score) of Bigot et al
- Predictors of Carvalho et al for Infection in a Hospitalized Patient with Systemic Lupus Erythematosus (SLE)
- Evaluation of a Patient with Systemic Lupus Erythematosus (SLE) with Hospitalization as the Presenting Event
- Bullous Systemic Lupus Erythematosus (SLE)
- SLE Risk Probability Index (SLERPI)
- Predictors of Floris et al for a Flare in Systemic Lupus Erythematosus (SLE)
- Geode in Rheumatoid Arthritis
- Criteria of Yamamoto and Oiwa for the Diagnosis of Polyarteritis Nodosa (PAN)
- Giant Cell Arteritis (GCA) Halo Score
- Prediction Model of Ing et al for Suspected Giant Cell Arteritis (GCA)
- Model of Weis et al for Identifying a Patient Whose Temporal Artery Biopsy is LIkely to Be Positive for Giant Cell Arteritis (GCA)
- Differential Diagnosis of Cutaneous Leukocytoclastic Vasculitis
- Neonatal Behcet's Disease
- Nomogram of Gendreau et al for Poor Outcome in a Patient with Systemic Vasculitis Involving the Gastrointestinal Tract
- Cutaneous Manifestations of ANCA-Associated Vasculitis
- Conditions Associated with HLA-B27
- Markers of Dumitru et al for Subclinical Heart Involvement in a Patient with Systemic Sclerosis
- Risk Factors of Mihai et al for Gangrene in a Patient with Systemic Sclerosis
- Risk Factors of Dein et al for Pseudo-Obstruction in Systemic Sclerosis
- Prognostic Factors of Sag et al for a Patient with Juvenile Dermatomyositis
- PRINTO Criteria for Clinically Inactive Juvenile Dermatomyositis
- Manual Muscle Testing on a Subset of Eight Muscles (MMT8) in Idiopathic Inflammatory Myopathies
- Muscle Biopsy Scoring System of Wedderburn et al for Juvenile Dermatomyositis: Inflammatory and Vascular Domains
- Muscle Biopsy Scoring System of Wedderburn et al for Juvenile Dermatomyositis: Muscle Fiber, Connective Tissue and Global Domains
- Skin Conditions Associated with Primary Immunodeficiencies: Eczema
- Skin Conditions Associated with Primary Immunodeficiencies: Abscess
- Skin Conditions Associated with Primary Immunodeficiencies: Disseminated Warts (HPV-Positive Skin Lesions)
- Skin Conditions Associated with Primary Immunodeficiencies: Granuloma Formation
- Skin Conditions Associated with Primary Immunodeficiencies: Mucocutaneous Candidiasis
- Skin Conditions Associated with Primary Immunodeficiencies: Nail Changes
- Skin Conditions Associated with Primary Immunodeficiencies: Hair Anomaly
- Skin Conditions Associated with Primary Immunodeficiencies: Psoriasis-Like
- Skin Conditions Associated with Primary Immunodeficiencies: SLE-like Skin Lesions
- Skin Conditions Associated with Primary Immunodeficiencies: Alopecia
- Skin Conditions Associated with Primary Immunodeficiencies: Mycobacterial Infection
- Mucocutaneous Conditions Associated with Primary Immunodeficiencies: Oral Changes
- Skin Conditions Associated with Primary Immunodeficiencies: Skin Ulcers
- Skin Conditions Associated with Primary Immunodeficiencies: Molluscum Contagiosum
- Skin Conditions Associated with Primary Immunodeficiencies: Skin Pigmentation
- Skin Conditions Associated with Primary Immunodeficiencies: Skin Rash
- Skin Conditions Associated with Primary Immunodeficiencies: Petechiae
- Skin Conditions Associated with Primary Immunodeficiencies: Miscellaneous Skin Changes
- Infections in the Differential Diagnosis of Adult Still's Disease
- Paraneoplastic Adult Still's Disease
- Refractory Systemic Onset Juvenile Idiopathic Arthritis (SJIA)
- FMF50 for Assessing Responsiveness of Therapy in Familial Mediterranean Fever (FMF)
- 2019 ACR and EULAR Criteria for IgG4-Related Disease: Exclusion Criteria
- 2019 ACR and EULAR Criteria for IgG4-Related Disease: Inclusion Criteria
- 2019 ACR and EULAR Criteria for IgG4-Related Disease: Criteria for Diagnosis
- Model of Hoi et al for Calculating the Probability of High Disease Activity (HDA) in Systemic Lupus Erythematosus (SLE)
- 2022 ACR/EULAR Classification Criteria for Giant Cell Arteritis (GCA)
- Post-Streptococcal Henoch Schonlein Purpura
- Clinical Features of Childhood Sjogren Syndrome
- Pseudo-Ankylosing Spondylitis Associated with Ochronosis
- Criteria of Oldroyd et al for Cancer Screening in a Patient with Idiopathic Inflammatory Myopathy
- Seronegative Polyarthritis Without Myositis Associated with Anti-NXP2 Antibodies
- Cancer Screening Protocol of Oldroyd et al in a Patient with Idiopathic Inflammatory Myopathy
- Differential Diagnosis of an Arthropathy Affecting the Spine and Peripheral Joints
- Criteria for Primary Natural Killer Cell Deficiency (NKD)
- Classification for Primary Natural Killer Cell Deficiency (NKD)
- Diagnostic Algorithm Natural Killer Cell Deficiency (NKCD)
- Anti-PL12 Syndrome (Anti-Aminoacyl-tRNA Synthetase Syndrome, ARS)
- Derived Neutrophil to Lymphocyte Ratio (dNLR)
- Systemic Inflammation Score (SIS) of Chang et al
- Memorial Sloan Kettering Prognostic Score (MPS)
- Pan-Immune-Inflammation Value (PIV)
- Predictors of Assuncao et al for Hospitalization of a Patient with Systemic Lupus Erythematosus (SLE)
- Model of Vanier et al for Predicting Rapid Radiographic Progression of Early Rheumatoid Arthritis
- Predictors of Khader et al for Remission of Rheumatoid Arthritis with Biologic Therapy
- Algorithm of Lecler et al for Diagnosis of Giant Cell Arteritis (GCA) by Imaging Studies
- Algorithm of Lecler et al for Diagnosis of Giant Cell Arteritis (GCA) by Imaging Studies: MRI Scoring
- Score of El-Dairi e al for Giant Cell Arteritis
- Conditions in the Differential Diagnosis of Giant Cell Arteritis
- Diagnostic Models of Czihal et al for Giant Cell Arteritis
- Clinical Criteria for Giant Cell Arteritis Based on the GiACTA Trial
- Score of Laskou et al for Diagnosis of Giant Cell Arteritis (GCA, Southend Score)
- Prognostic Model of Levine et al for Acute Graft-versus-Host Disease Using Serum Biomarkers (Ann Arbor Score)
- Day 100 Score of Metafuni et al for Prediction Moderate to Severe cGVHD After a Hematopoietic Cell Transplant
- High-Risk Indicators of Fan et al for Central Nervous System (CNS) Involvement in Primary Sjogren's Syndrome
- Clinical Findings of Fan et al for Central Nervous System (CNS) Involvement in Primary Sjogren's Syndrome
- Nomogram of Ye et al for Predicting Axial Spondyloarthritis
- Systemic Sclerosis Sine Scleroderma (ssSSc)
- ONCOREUM Score of Civino et al for Distinguishing Childhood Cancer with Arthropathy from Juvenile Idiopathic Arthritis (JIA)
- Model of Xu et al for Predicting Bloodstream Infection (BSI) in a Patient with Fever of Unknown Origin (FUO)
- Model of Zhang et al for Enteritis in Systemic Lupus Erythematosus (SLE)
- Equations of Pu et al for Converting the DAS28CRP and DAS28ESR to the SDAI
- Predictors of Khader et al for Remission in a Patient with Rheumatoid Arthritis Treated with a Biologic
- French Vasculitis Study Group Relapse Score (FRS) of Samson et al for Granulomatosis with Polyangiitis or Microscopic Polyangiitis
- E-CASE Score of Takahashi et al for the Diagnosis of Eosinophilic Granulomatosis with Polyangiitis (EGPA)
- Model of Moudrous et al for Diagnosis of Giant Cell Arteritis (GCA)
- JSpAflare Measure of Weiss et al for a Flare of Juvenile Spondyloarthritis
- Morphea Activity Measure for a Pediatric Patient with Morphea: Domain Subscore
- Morphea Activity Measure for a Pediatric Patient with Morphea: Total Activity Score
- Risk Factors of Xie et al for Mortality in a Patient with Anti-MDA5 Antibody Positive Dermatomyositis
- Diagnostic Algorithm of Daghor-Abbaci et al for Adult-Onset Still's Disease (AOSD)
- Model of van Straalen et al for Predicting Juvenile Idiopathic Arthritis (JIA)
- Predictors of Fredeau et al for Progression from Discoid Lupus Erythematosus to Systemic Lupus Erythematosus
- Comedonic Lupus Erythematosus (Comedonic Discoid Lupus)
- Takayasu Arteritis Integrated Disease Activity Index (TAIDAI) of Marvisi et al
- Positron Emission Tomography Vascular Activity Score (PETVAS)
- International Criteria for Behcet's Disease (ICBD)
- Conditions That May Mimic a Large Vessel Vasculitis
- Nomogram of Bai et al for Survival After Ankylosing Spondylitis Cervical Fracture with Neurologic Impairment (ASCF-NI)
- Scleromyositis (Overlap Syndrome of Scleroderma and Dermatomyositis/Polymyositis
- DOCK-8 Deficiency Primary Immunodeficiency Syndrome
- Autoimmune Hemolytic Disease (AIHD) Associated with Myelodysplastic Syndrome (MDS)
- Autoimmune Hemolytic Disease (AIHD) in Infectious Mononucleosis (Epstein Barr Virus, EBV)
- Endothelial Activation and Stress Index (EASIX) and Its Variations in the Prediction Cytokine Release Syndrome After Chimeric Antigen Receptor T (CART) Cell Therapy
- Autoimmune Progesterone Dermatitis (APD)
- Risk Factors of Lavigne et al for Systemic Adverse Effects Following Ultrasound or Fluoroscopy Guided Glucocorticoid Injection
- Neutrophil to Albumin and Neutrophil Percent to Albumin Ratios
- Neutrophil to Lymphocyte Ratio (NLR) to Albumin Ratio
- Lymphocyte-Albumin-Neutrophil Ratio (LANR)
- CARWL Index (CRP to Albumin Ratio and Weight Loss)
- Inflammation-Immunity-Nutrition Score (IINS) of Zhang et al
- Inflammatory Burden Index (IBI) of Xie et al
- Clinical Features of the Anti-GQ1b Antibody Syndrome
