Results 181 to 190 of about 5,699 (211)
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PATH TO DIAGNOSIS IN FAMILIAL MEDITERRANEAN FEVER (FMF)
[No abstract available]Karup, Sejla +6 more
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[Familial Mediterranean Fever (FMF): from diagnosis to treatment].
Sante (Montrouge, France), 2005Familial Mediterranean Fever (FMF), also known as paroxysmal polyserositis, is an autosomal recessive disease affecting mainly Mediterranean populations (Jews, Armenians, Arabs, Turks). It is characterised by recurrent crises of fever and serosal inflammation, leading to abdominal, thoracic or articular pain.
Myrna, Medlej-Hashim +3 more
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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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Familial Mediterranean Fever (FMF): a single centre retrospective study in Amsterdam.
The Netherlands journal of medicine, 2019Familial Mediterranean Fever (FMF) is the earliest described and most prevalent hereditary auto-inflammatory disease. Its clinical presentation is diverse, leading to possible delay in diagnosis and treatment. Due to immigration, FMF became common in non-Mediterranean European regions.
Hageman, I.M.G. +4 more
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Ethnic Distribution and Amyioidosis in Familial Mediterranean Fever (FMF)
Pathologia et Microbiologia, 2010H, HELLER, E, SOHAR, M, PRAS
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Trends in colchicine treatment in Familial Mediterranean fever (FMF)
2008[No abstract available]
La Regina, M. +3 more
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Y688X, the first nonsense mutation in familial Mediterranean fever (FMF)
Human Mutation, 2000C, Notarnicola +3 more
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