Results 151 to 160 of about 846,391 (207)

Characterizing MEFV gene variants in Jordanian patients with Familial Mediterranean Fever. [PDF]

Hum Genomics
Alwazani WA, Fuqaha NA, Medras Z, Rjoub YA, Altaany K.   +4 more
europepmc   +1 more source

The clinical significance of heterozygous E148Q variant in patients with familial Mediterranean fever. [PDF]

Clin Rheumatol
Aktaş A, Aljaber Y, Avad H, Cansu DÜ, Bal C, Korkmaz C.   +5 more
europepmc   +1 more source

Evidence of the role of Midkine and Pleiotrophin in the pathogenesis of Familial Mediterranean Fever. [PDF]

Eur J Pediatr
Abdallah ZY, Eldeen GN, Sokkar MF, Abdelkawy RFM, Lotfy RS, Hussein SH, Hamed K, El-Bassyouni HT.   +7 more
europepmc   +1 more source

Association Between Familial Mediterranean Fever and P-Wave Dispersion Under Colchicine Treatment. [PDF]

Diagnostics (Basel)
Cüre O, Durak H, Çetin M, Kızılkaya B.   +3 more
europepmc   +1 more source

The effect of colchicine on micronutrients in children with newly diagnosed familial Mediterranean fever. [PDF]

J Pediatr (Rio J)
Kaba Ö, Tanatar A, Koç R, Karadağ ŞG, Çakan M, Aktay Ayaz N.   +5 more
europepmc   +1 more source

Subclinical inflammation in pediatric familial Mediterranean fever: predictors and follow-up results of a retrospective single-center cohort study. [PDF]

Clin Rheumatol
Bahçeci O, Aydin F, Taş Aslan Ö, Sarisoy D, Erorhan E, Özçakar ZB.   +5 more
europepmc   +1 more source

Polyarteritis nodosa in patients with Familial Mediterranean Fever (FMF): A concomitant disease or a feature of FMF?

Seminars in Arthritis and Rheumatism, 2001
Familial Mediterranean Fever (FMF) is caused by mutations in the gene encoding pyrin and is characterized by self-limited, recurrent attacks of fever and serositis. Vasculitis has been increasingly reported in FMF. A study evaluating the prognosis in FMF and polyarteritis nodosa (PAN) patients has not been reported previously.To determine the special ...
Eldad Ben-Chetrit, Nesrin Besbas, K Tinaztepe   +2 more
exaly   +4 more sources

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Dominant inheritance in two families with familial Mediterranean fever (FMF)

American Journal of Medical Genetics Part A, 1995
AbstractFamilial Mediterranean fever (FMF) is an autosomal‐recessive disease which affects almost exclusively people of Mediterranean and Middle Eastern origin. We examined the possibility of a dominant inheritance of FMF among our 3,000 patients in Israel.Two hundred forty FMF patients were members of 77 families in which the disease affected more ...
Y, Yuval, M, Hemo-Zisser, D, Zemer, E, Sohar, M, Pras   +4 more
exaly   +3 more sources