Results 51 to 60 of about 846,391 (207)
Rheumatoid Arthritis and Familial Mediterranean Fever or Sacroiliitis Accompanied by FMF
Case Reports in Rheumatology, 2013 The coexistence of rheumatoid arthritis (RA) and familial Mediterranean fever (FMF) has been rarely seen in case reports in the literature. Herein, we wanted to present a patient who had been followed up and treated as RA, but on investigation we concluded that he really had FMF and its joint complaints associated with sacroiliitis.
Ali Şahin +2 more
openaire +3 more sources
Colchicine has Dose‐Dependent Therapeutic Effects in a LPS‐Induced Experimental Endotoxemia Model
Pharmacology Research &Perspectives, Volume 14, Issue 2, April 2026.ABSTRACT Colchicine is an ancient medication that has long been used for anti‐inflammatory properties. Because of unfavorable and toxic consequences of colchicine, selecting an appropriate dose is critical. The effects of three different doses (0.5, 1 or 5 mg/kg) of colchicine were evaluated.
Meliksah Demir +5 more
wiley +1 more source
Familial Mediterranean Fever (FMF) in Turkey Results of a Nationwide Multicenter Study
, 2005 : Familial Mediterranean fever (FMF) is an autosomal recessive disease that is prevalent among eastern Mediterranean populations, mainly non-Ashkenazi Jews, Armenians, Turks, and Arabs.
Turkish FMF Study Group*
core +1 more source
Nonalcoholic fatty liver disease and familial Mediterranean fever: Are they related? [PDF]
Srpski Arhiv za Celokupno Lekarstvo, 2012 Introduction. Familial Mediterranean fever (FMF) is a periodic febrile disease characterized by acute recurrent episodes of serositis. Liver disease is not considered a part of the spectrum of clinical manifestations of FMF. Objective.
Sarkis Cihat +7 more
doaj +1 more source
Pediatric Allergy and Immunology, Volume 37, Issue 8, August 2026.
Blandine Monjarret +12 more
wiley +1 more source
Internal Medicine Journal, Volume 56, Issue 4, Page 589-597, April 2026.Abstract Background To identify early diagnostic clues, we analysed cerebrospinal fluid and serum biomarkers in patients with autoimmune glial fibrillary acidic protein astrocytopathy (GFAP‐A) and compared biomarker trends with those in patients with viral meningoencephalitis, tuberculous meningoencephalitis, and anti‐N‐methyl‐D‐aspartate receptor ...
Siruo Guo +3 more
wiley +1 more source
Concurrent TNFRSF1A R92Q and pyrin E230K mutations in a child with multiple sclerosis [PDF]
, 2010 We report a 16-year-old female patient with a severe course of multiple sclerosis and concomitant symptoms suggestive of a hereditary autoinflammatory disease.
K Huss +16 more
core +1 more source
Familial Mediterranean Fever and Transverse Myelitis: A Causal Relation?
Neurology and Therapy, 2023 Familial Mediterranean fever (FMF) is a rare autoinflammatory disorder characterized mainly by recurrent self-limited episodes of fever and polyserositis.
Ali Motahharynia +4 more
doaj +1 more source
Journal of Cellular and Molecular Medicine, Volume 30, Issue 7, April 2026.ABSTRACT Glioblastoma (GB), defined as IDH‐wildtype CNS WHO grade 4 tumour according to the 2021 WHO classification of CNS tumours, remains a uniformly lethal malignancy in which the efficacy of temozolomide (TMZ) continues to be constrained by both intrinsic tumur biology and the pharmacological barrier imposed by the blood–brain barrier (BBB).
Fabiola De Luca +7 more
wiley +1 more source
Tuberculosis Presenting as Migratory Arthritis: A Case Report from Iraq
Clinical Case Reports, Volume 14, Issue 3, March 2026.ABSTRACT Extrapulmonary tuberculosis is uncommon, and musculoskeletal involvement presenting as migratory arthritis is particularly rare in immunocompetent individuals, often leading to misdiagnosis and delayed treatment. We report the case of a 66‐year‐old man with diabetes mellitus who presented with recurrent migratory inflammatory arthritis ...
Farah Jaafar Mahdi +7 more
wiley +1 more source