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Familial Mediterranean fever in Arab children: The high prevalence and gene frequency
European Journal of Pediatrics, 1996Over a period of 3 years, 192 children with familial Mediterranean fever were prospectively studied. Of these, 106 (55%) were girls and 86 (45%) were boys. The prevalence was 1:2600 children with a gene frequency of 1:50. The age at onset ranged between 4 months and 16 years.
M O, Rawashdeh, H A, Majeed
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The Familial Mediterranean Fever (MEVF) Gene as a Modifier of Crohn's Disease
The American Journal of Gastroenterology, 2005Crohn's disease (CD) has been reported to be more frequent among non-Ashkenazi Jewish patients suffering from familial Mediterranean fever (FMF). Interestingly, functional similarities between the CD susceptibility gene (NOD2/CARD15) and the FMF gene (MEFV) have been described: both belong to the death domain containing protein family, important in the
Herma, Fidder +8 more
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Assessment of pyrin gene mutations in Turks with familial Mediterranean fever (FMF)
Human Mutation, 1998Familial Mediterranean fever (FMF) is an autosomal recessive disease clinically characterized by recurrent short self-limited attacks of fever accompanied by peritonitis, pleurisy, and arthritis and can lead to amyloidosis and renal failure in the longer term. It is prevalent mainly in non-Ashkenazi Jews, Armenians, Turks, and Arabs. Due to the lack of
X, Chen +7 more
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[From gene to disease; marenostrine and familial Mediterranean fever].
Nederlands tijdschrift voor geneeskunde, 2000Familial mediterranean fever (FMF) is an autosomal recessive hereditary disorder associated with mutations in the gene on chromosome 16 encoding the protein pyrine (marenostrine). Marenostrine is thought to stimulate the production of an inactivator of a chemotactic factor (possibly C5a). The mutations result in ongoing inflammation, a hallmark of FMF.
M H, Breuning, E, Bakker
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MEFV Gene Mutations in Familial Mediterranean Fever Patients: Erzincan Experience
Erzincan Üniversitesi Fen Bilimleri Enstitüsü DergisiAilesel Akdeniz Ateşi, MEFV geninde meydana gelen mutasyonların yol açtığı otozomal resesif geçişli otoinflumatuar multisistemik genetik bir hastalıktır. Ülkemizde sık görülen bir hastalık olmakla birlikte hastalığa sebep olan mutasyonların tipi ve sıklıkları bölgesel olarak farklılık göstermektedir.
Abdussamed Yasin Demir, Özlem Admış
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MEFV gene mutation spectrum in familial Mediterranean fever (FMF)
2011PubMed ID ...
Coker, I. +4 more
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Cancer epigenetics in clinical practice
Ca-A Cancer Journal for Clinicians, 2023Veronica Davalos, Manel Esteller
exaly
[Familial Mediterranean fever--from gene test to clinical aspects].
Praxis, 2001Familial Mediterranean Fever (FMF) is a genetically defined disease affecting mostly families of jewish, turkish or armenian origin whose ancestors originate from the mediterranean basin. The first officially acknowledged description was given by SIEGAL in 1945 but previous cases were reported since 1908.
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