Results 161 to 170 of about 6,939 (203)

The Relationship Between Gene Subtypes, Symptoms, and Cardiac Function in Patients with Familial Mediterranean Fever. [PDF]

J Clin Med
Kızılkaya B, Cure O, Durak H, Çetin M.   +3 more
europepmc   +1 more source

Familial Mediterranean Fever: A Comprehensive Review of Pathogenesis, Genetics, and Epigenetic Regulation. [PDF]

Balkan Med J
Ugurlu S, Kilinc OC, Karacan I, Parlar K.   +3 more
europepmc   +1 more source

Co-occurrence of autoimmune diseases and metabolic disorders in familial mediterranean fever patients: review of literature and case reports. [PDF]

Front Immunol
Chaaban A, Baalbaki N, Narch R, Eldawra E, Kobeissy PH, Ibrahim JN.   +5 more
europepmc   +1 more source

Evaluation of pediatric FMF patients with biallelic pathogenic exon 10 variants: focus on chest pain. [PDF]

Eur J Pediatr
Tunce E, Atamyıldız Uçar S, Çağlar Eİ, Kara Çanlıoğlu N, Sözeri B.   +4 more
europepmc   +1 more source

Comparative analysis of exon 10 and non-exon 10 variants in children with familial mediterranean fever: a retrospective cohort study. [PDF]

Eur J Pediatr
Menentoğlu B, Arık SD, Prencuva Akyürek P, Akgün Ö, Aktay Ayaz N.   +4 more
europepmc   +1 more source

Inflammatory bowel disease in children with MEFV gene variants

Inflammatory bowel disease in children with MEFV gene variants
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Inflammatory bowel disease of children with MEFV gene variants

Inflammatory bowel disease of children with MEFV gene variants
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MEFV gene mutations in Turkish children with juvenile idiopathic arthritis

European Journal of Pediatrics, 2013
Mutations of the Mediterranean fever (MEFV) gene, which encodes pyrin protein, leads to familial Mediterranean fever (FMF) and a connection between MEFV mutations and rheumatic diseases has been suggested. The aim of this study was to explore the frequency and clinical significance of MEFV mutations in children with juvenile idiopathic arthritis (JIA).
Elif, Comak, Cagla Serpil, Dogan, Sema, Akman, Mustafa, Koyun, Arife Uslu, Gokceoglu, Ibrahim, Keser   +5 more
openaire   +4 more sources

The association of TNFRSF1A gene and MEFV gene mutations with adult onset Still’s disease

Rheumatology International, 2012
Adult onset Still's disease (ASD) is a systemic inflammatory disorder of unknown etiology. ASD is characterized by fever with unknown etiology, rash, arthritis, and involvement of several organ systems. FMF and TRAPS are two important autoinflammatory diseases which characterized with recurrent inflammatory attacks.
Ekmekci, Sema Sirma, Azakli, Hulya, YAZICI, AYTEN, ERBAĞ, Gokhan, Abaci, Neslihan, COŞAN, Fulya, Ustek, Duran, ÇEFLE, AYŞE, YILMAZER, Baris, Emrence, Zeliha   +9 more
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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