Results 201 to 210 of about 30,113 (242)
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Molecular Study of FMF Patients in Armenia
Current Drug Target -Inflammation & Allergy, 2005Familial Mediterranean Fever (FMF, MIM 249100), or Periodic disease, is a recessively transmitted and ethnically restricted condition prevalent in population from the Mediterranean decent. FMF notoriously has been hard to diagnose until mutations in the MEFV gene have been identified and as a tremendous help are used for the diagnosis of difficult ...
T, Sarkisian +2 more
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Febbre Mediterranea Familiare (FMF)
Acta geneticae medicae et gemellologiae, 1960RiassuntoNell'articolo vengono esposte le nostre osservazioni a proposito della FMF in base alle quali abbiamo inquadrato una nuova entità nosologica.Applicando dei criteri diagnostici definiti (a - attacchi febbrili ricorrenti accompagnati da b - dolori addominali, toracici o articolari) escludendo fattori causali noti, abbiamo diagnosticato la ...
Ezra Sohar +4 more
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Familiäres Mittelmeerfieber (FMF)
2010Das familiare Mittelmeerfieber ist eine autosomal rezessiv vererbte Erkrankung, die vor allem bei Menschen aus dem ostlichen Mittelmeer vorkommt. Das FMF ist gekennzeichnet durch meist in unregelmasigen Abstanden auftretende Fieberattacken ohne erkennbare Ursache, einhergehend mit Arthritis, Peritonitis und/oder seltener Pleuritis.
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Canakinumab In Patients With FMF
2013[No abstract available]
Uğurlu, Serdal +4 more
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European Journal of Neurology, 2011
To describe and characterize the association between familial Mediterranean fever (FMF) and multiple sclerosis (MS). The patient registry of The National Center for FMF was screened for the coexistence of FMF and MS. Tel-Hashomer criteria were used for the diagnosis of FMF, and FMF severity was evaluated, using the simplified FMF severity scale ...
G, Yahalom +7 more
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To describe and characterize the association between familial Mediterranean fever (FMF) and multiple sclerosis (MS). The patient registry of The National Center for FMF was screened for the coexistence of FMF and MS. Tel-Hashomer criteria were used for the diagnosis of FMF, and FMF severity was evaluated, using the simplified FMF severity scale ...
G, Yahalom +7 more
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Neurospora fmf-1: lure and lore
Journal of GeneticsThe Neurospora crassa fmf-1 mutant has a unique phenotype. It arrests sexual development when the fruiting bodies (perithecia) attain only 40% of their normal diameter, regardless of whether the mutant participates in a cross with the wild type (fmf-1 x fmf-1+) as the male or female parent.
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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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Secondary amyloidosis due to FMF.
Hepato-gastroenterology, 2007Familial 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
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