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[Amyloidosis of familial Mediterranean fever (FMF)--insights to FMF phenotype II].
Harefuah, 2007Amyloidosis is the most grievous manifestation of Familial Mediterranean Fever (FMF), occurring in a high proportion of untreated patients. Continuously elevated serum amyloid A (SAA) levels during remissions, rather than a pulsatile rise during FMF attacks, underlies the development of amyloidosis.
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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
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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
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Active learning for OPM in FMF systems
Physical Communication, 2023Mohammad Ali Amirabadi +2 more
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Familial Mediterranean Fever (FMF)
2014Familial Mediterranean Fever (FMF) is an autosomal recessive genetic disease that affects males and females. FMF gene is on the short arm of chromosome 16. It is most often found in Jews, Arabs, Turks, and Armenians. Amyloidosis is charecterized by the deposition of a particular protein between the cells in the tissue.
ALBAYRAK, Onur, ÇÜRÜK, M. Akif
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The arthritis of familial mediterranean fever (FMF)
Arthritis & Rheumatism, 1966H, Heller +7 more
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