Results 171 to 180 of about 6,236 (217)

Cachexia as an unusual presentation of familial Mediterranean fever: A case report. [PDF]

World J Clin Cases
Sira AM, Shoeir SA, Sira MM.
europepmc   +1 more source

Familial Mediterranean Fever: A Diagnostic and Therapeutic Challenge. [PDF]

Cureus
Sia R.
europepmc   +1 more source

A semi-automated ASC speck assay to evaluate pyrin inflammasome activation. [PDF]

Clin Transl Immunology
Dai P, Skinner O, Lin X, Telfser A, Ruiz-Diaz S, Saldanha RG, Frith K, Lin MW, Preece K, Gray PE, Pinzon-Charry A, Sullivan A, Adelstein S, Tong WW, Parker MJ, Girgis L, Wainstein B, Ojami S, Deenick EK, Goldstein LD, Rogers MJ, Phan TG.   +21 more
europepmc   +1 more source

Idiopathic recurrent pericarditis in children: a tertiary care cohort highlighting the emergence and effectiveness of interleukin-1 blockade. [PDF]

Eur J Pediatr
Gunalp A, Akay N, Kirali M, Torunoglu Z, Aslan E, Gul U, Konte EK, Senturk NGK, Yildiz M, Haslak F, Adrovic A, Sahin S, Barut K, Dedeoglu R, Kasapcopur O.   +14 more
europepmc   +1 more source

Case Report: Diagnostic difficulties, treatment, and association of the MEFV E148Q variant in a patient with PASH syndrome. [PDF]

Front Med (Lausanne)
Qin Q, Cao C, Liang J, Li B, Su J.
europepmc   +1 more source

Pediatric COPA Syndrome Overlapping With Heterozygous Familial Mediterranean Fever: A Dual Inflammatory Disorder. [PDF]

Case Rep Pediatr
Khalaf L, Lahlouh M, Abdul-Haleem K, Hamdan M.   +3 more
europepmc   +1 more source

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Clinical significance of MEFV gene variation R202Q

Clinical Rheumatology, 2021
The aim of this study was to evaluate the phenotypic features and the clinical significance of the R202Q mutation of the MEFV gene.We retrospectively reviewed the medical records of Familial Mediterranean Fever patients with M694V/- and M694V/R202Q mutations.
Kandur, Yasar, Kocakap, Derya Beyza Sayin, Alpcan, Aysegul, Tursun, Serkan   +3 more
openaire   +3 more sources

Clinical significance of MEFV mutations in ankylosing spondylitis

Joint Bone Spine, 2009
The aim of the present study was to investigate the prevalence of MEFV gene mutations in patients with ankylosing spondylitis (AS) and to assess the clinical significance of the MEFV gene mutations in AS.Eighty AS patients and 85 healthy controls were examined for 12 common MEFV mutations via strip-assay technique.
Gamze Alayli, Serbulent Yigit
exaly   +4 more sources

MEFV Gene Mutations in a Patient with Eosinophilic Gastroenteritis

Southern Medical Journal, 2010
Eosinophilic gastroenteritis (EG) is an uncommon gastrointestinal disease affecting both children and adults. The underlying molecular mechanism predisposing to the clinical manifestation of eosinophilic gastroenteritis is unknown. A 39-year-old man who was followed up with the diagnosis of familial Mediterranean fever (FMF) was admitted to our clinic ...
Gulay, Kocak, Erdem, Kocak, Seref Rahmi, Yilmaz, Seyfettin, Koklu, Murat, Duranay, Funda, Yalcin, Yildiz, Albayrak   +6 more
openaire   +2 more sources