Results 111 to 120 of about 5,699 (211)

Familial Mediterranean fever: New phenotypes

, 2012
Familial Mediterranean fever (FMF) is an inherited autosomal recessive disorder, ethnically restricted and commonly found among individuals of Mediterranean descent, caused by MEditerranean FeVer gene (MEFV) mutations on chromosome 16.
Manna, Raffaele, Soriano, Alessandra
core   +1 more source

Assessment of Interleukin-33 Levels in Patients with Familial Mediterranean Fever

Romanian Journal of Internal Medicine
This study was designed to evaluate the relationship between serum interleukin-33 (IL-33) levels and clinical features of the disease in patients with Familial Mediterranean Fever (FMF).
Demirezen Asil, Güler Aslihan Avanoğlu, Karadeniz Hazan, Kavutçu Mustafa, Tufan Abdurrahman   +4 more
doaj   +1 more source

Familial Mediterranean fever

, 2002
Background. The pathogenesis of familial Mediterranean fever (IMF) is unknown, and since no specific laboratory test is yet available, the diagnosis of FMF remains clinical.
Cetinkaya, R, Odabas, AR, Bilen, Habib, Selcuk, Y   +3 more
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Familial Mediterranean fever

, 2003
Familial Mediterranean fever (FMF) is the most frequent periodic syndrome characterized by recurrent attacks of polyserositis. Fever, abdominal pain, chest pain, and arthritis/arthralgia are the leading symptoms.
Bakkaloglu, A
core   +1 more source

Diagnosis of Familial Mediterranean Fever (FMF) with Fuzzy Logic

Ikonion Journal of Mathematics
In this work, we developed a fuzzy decision-making method to help diagnose of Familial Mediterranean Fever (FMF), with the support of a doctor who is an expert in the field, and we briefly called it the FMF fuzzy diagnosis method (FMF-FDM). In the decision-making mechanism, we used the Mamdani method, which is one of the fuzzy logic inference methods.
Ebru Gülender, Naim Cagman, Berrin Akın   +2 more
openaire   +1 more source

Current therapeutic options for managing familial Mediterranean fever

, 2015
Introduction: Familial Mediterranean fever (FMF) is a monogenic autoinflammatory disease characterized by recurrent attacks of fever and serositis. Although colchicine prevents the recurrence of FMF attacks and the development of secondary amyloidosis ...
ÖZEN, SEZA, BİLGİNER, YELDA, Batu, EZGİ DENİZ, Arici, ZEHRA SERAP   +3 more
core   +1 more source

Sacroiliitis in familial Mediterranean fever: an unusual presentation in childhood

The Turkish Journal of Pediatrics, 1999
Familial Mediterranean fever (FMF) is an autosomal recessively transmitted disease characterized by attacks of fever and serositis. The course of arthritis, which is a common manifestation of FMF, is generally benign.
N Beşbaş, S Ozdemir, I Saatçi, A Bakkaloğlu, S Ozen, U Saatçi   +5 more
doaj  

Lithium prophylaxis in familial Mediterranean fever

, 1979
Familial Mediterranean fever (FMF), also called familial paroxysmal polyserositis or periodic disease, is a heredo-familial disorder of recurrent course, peculiar ethnic distribution and unknown etiology.
Loukopoulos, D.L., Christodoulou, G.N., Madianos, M.G., Stefanis, C.N.   +3 more
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MULTIPLE SCLEROSIS ASSOCIATED WITH FAMILIAL MEDITERRANEAN FEVER

, 1997
IN THİS PAPER WE PRESENT TWO PATİENTS WİTH RELAPSİNG REMİTTİNG DEFİNİTE MULTIPLE SCLEROSIS WHO HAD FAMILIAL MEDİTERRANEAN FEVER (FMF) BEGİNNİNG İN ...
YÜCE, AYŞE, İDİMAN, EGEMEN, Tataroğlu, M. Cengiz, KUTLUK, M.KÜRŞAT, Tankurt, İ. Ethem, İDİMAN, FETHİ   +5 more
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Familial Mediterranean fever : a common hereditary disease in Malta

, 2008
Familial Mediterranean Fever (FMF), also known as recurrent polyserositis, is an autosomic recessive disease affecting the inflammatory pathway Other related inherited conditions include hyperimmunoglobulinaemia D with periodic fever syndrome (HIDS) and ...
Scerri, Christian A.
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