Results 131 to 140 of about 6,939 (203)

Homozygous MEFV Gene Variant and Pyrin-Associated Autoinflammation With Neutrophilic Dermatosis: A Family With a Novel Autosomal Recessive Mode of Inheritance.

JAMA Dermatol, 2021
Vahidnezhad H, Youssefian L, Saeidian AH, Ziaee V, Mahmoudi H, Parvaneh N, Ashjaei B, Shahrokh S, Kamyab Hesari K, Soltani Zangbar M, Yousefi M, Zeinali S, Uitto J.   +12 more
europepmc   +1 more source

Exploring the Role of MEFV Gene Mutations in Pediatric Drug-Resistant Epilepsy. [PDF]

Iran J Child Neurol
Habibi A, Raeeskarami SR, Hadipour F, Hadipour Z, Salehzadeh F, Shervin Badv R, Ziaee V, Sadeghi P.   +7 more
europepmc   +1 more source

Assessment of Surrogate Markers for Cardiovascular Disease in Familial Mediterranean Fever-Related Amyloidosis Patients Homozygous for M694V Mutation in MEFV Gene. [PDF]

Life (Basel), 2022
Sahin S, Romano M, Guzel F, Piskin D, Poddighe D, Sezer S, Kasapcopur O, Appleton CT, Yilmaz I, Demirkaya E.   +9 more
europepmc   +1 more source

The MEFV gene and clonal myeloid disorders

The Turkish Journal of Pediatrics, 2012
openaire   +4 more sources

Anakinra-Dependent Recurrent Pericarditis: The Role of the R202Q Variant of the MEFV Gene. [PDF]

J Clin Med
Andreis A, Dossi FC, De Ferrari GM, Alunni G, Imazio M.   +4 more
europepmc   +1 more source

Increasing Importance of Genotype-Phenotype Correlations Associated with Common and Rare MEFV Gene Mutations in FMF Patients in the Last Thirty Years. [PDF]

J Clin Med
Yildirim S, Bekis Bozkurt H, Erguven M.
europepmc   +1 more source

A patient with P369S/R408Q variants in the MEFV gene presented with clinical features of Kikuchi disease and Mollaret meningitis, successfully treated with colchicine. [PDF]

BMC Neurol
Handa H, Sugiyama A, Kubosawa H, Nakagawa Y, Kishida D, Uzawa A, Aotsuka A, Kuwabara S.   +7 more
europepmc   +1 more source

Generation of iPSCs from a Patient with the M694V Mutation in the MEFV Gene Associated with Familial Mediterranean Fever and Their Differentiation into Macrophages. [PDF]

Int J Mol Sci
Grigor'eva EV, Karapetyan LV, Malakhova AA, Medvedev SP, Minina JM, Hayrapetyan VH, Vardanyan VS, Zakian SM, Arakelyan A, Zakharyan R.   +9 more
europepmc   +1 more source

Coexistence of PFAPA syndrome and FMF in Armenian children [PDF]

, 2015
G Amaryan, N Mkrtchyan, T Sarkisian
core   +2 more sources

MEFV gene mutation spectrum in patients with familial mediterranean fever

Pediatrics & Neonatology, 2023
openaire   +3 more sources