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From the literature - FMF

2014
Familial Mediterranean Fever (FMF) is the most common hereditary autoinflammatory syndrome. It is caused by mutations in the MEFV gene which en- codes the pyrin protein, which has an important role in the activation of IL-1β (1). The condition manifests as attacks of serositis, com- monly involving the abdomen, chest or joints, typically accompanied by
GALLIZZI, Romina, Mirella Crapanzano
openaire   +1 more source

Secondary amyloidosis due to FMF.

Hepato-gastroenterology, 2007
Familial Mediterranean fever (FMF) is an ethnically restricted disease with an autosomal recessive inheritance characterized by recurrent attacks of fever, painful manifestations in the abdomen, chest and joints. The disease affects mainly non-Ashkenazi Jews, Armenians, Turks Arabs and other people of Mediterranean origin.
Ozlem, Yonem, Yusuf, Bayraktar
openaire   +1 more source

FMF

2009
Robert J. Desnick   +48 more
openaire   +2 more sources

FMF-Kongreß Hamburg '94

nachbarsprache niederländisch, Bd. 9 Nr. 2 (1994)
openaire   +1 more source

Febbre Mediterranea familiare (FMF)

2012
Familial Mediterranean fever (FMF) is also called recurrent polyserositis, and its prominent features include brief recurrent episodes of peritonitis, pleuritis, and arthritis, usually with accompanying fever. FMF occurs within individuals of Mediterranean descent than in persons of any other ethnicity, and genetic testing is now available for ...
Cantarini, L.   +7 more
openaire   +1 more source

Follikuläre Mycosis fungoides (FMF)

Der Hautarzt, 2001
F. Zipprich   +3 more
openaire   +1 more source

Familial Mediterranean fever (FMF) phenotype in patients homozygous to the MEFV M694V mutation.

European Journal of Medical Genetics, 2019
C. Grossman   +3 more
semanticscholar   +1 more source

On demand use of anakinra for attacks of familial Mediterranean fever (FMF)

Clinical Rheumatology, 2018
H. Babaoğlu   +9 more
semanticscholar   +1 more source

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