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Abstract Number: 1320
Activity Tracker Bracelets Captures Familial Mediterranean Fever Attacks and Their Impact on Daily Physical Activities
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Abstract Number: 1321
Clinical and Genetic Analysis of the Patients Mimicking Familial Mediterranean Fever
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Abstract Number: 1322
Comparison of Serum Hepcidin and Calprotectin Levels in Patients with Familial Mediterranean Fever (FMF) and Healthy Subjects
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Abstract Number: 1323
Evaluation of Prolidase and HIF-1α Levels in Patients with Familial Mediterranean Fever (FMF)
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Abstract Number: 1324
Anakinra Treatment in Refractory Cases of Adult-Onset Still Disease: Case Series
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Abstract Number: 1325
Canakinumab Treatment in Adult-Onset Still’s Disease: Case Series
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Abstract Number: 1326
Does Testing for SAA Is More Beneficial Than CRP for the Follow-up of Patients with Familial Mediterranean Fever ?
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Abstract Number: 1327
The Effect of Etoposide on Inducing Remission in Refractory Adult-Onset Still’s Disease: A Retrospective, Single-Center Study
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Abstract Number: 1328
Recurrent Pericarditis: A Challenge in Autoinflammatory Disease Clinic and the Role of Anakinra
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Abstract Number: 1329
Combination of Methotrexate and Leflunomide in Refractory Chronic Adult Onset Still’s Disease: Case Series and Literature Review
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Abstract Number: 1330
Dyskeratotic Cells in Persistent Pruritic Skin Lesions Are Apoptotic and Associated with High Levels of Serum IL-18, and Possibly Predict the Outcomes in Adult-Onset Still’s Disease
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Abstract Number: 1331
Moving from Dermatomyositis Associated with Anti-Melanoma Differentiation-Associated Gene 5 Antibody to Anti-Melanoma Differentiation-Associated Gene 5 Syndrome
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Abstract Number: 1332
Proteomic Discovery Analysis Identifies Unique Proteins and Pathways Correlating with Different Clinical Activity and Damage Measures in Juvenile Dermatomyositis (JDM)
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Abstract Number: 1333
Abnormal Function of High Density Lipoproteins in Idiopathic Inflammatory Myopathies
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Abstract Number: 1334
Low Density Granulocytes As Biomarkers of Disease Activity and Damage in Patients with Idiopathic Inflammatory Myopathies
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