منابع مشابه
P01-043 – Comparative characteristic of FMF and FMF with HSP
Methods Clinical studies conducted in 61 non complicated of amyloidosis FMF children in the Republican FMF Children Center, Center “Arabkir”. The age of the patients varies from 5-15. Three patients of FMF are accompanied with HSP. We are selected as a control group of 11 healthy people in practice.Biochemical studies carried out in Hematological Center of Armenia. In erythrocytes of membrane w...
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We give an overview of the running time analysis of the random divide-and-conquer algorithm FIND or QUICKSELECT. The results concern moments, distribution of FIND’s running time, the limiting distribution, a stochastic bound and the key: a stochastic fixed point equation.
متن کاملFMF: an update
Familial Mediterranean fever (FMF) is the most common autoinflammatory disease over the world. This autosomal recessively inherited disease is due to mutations in the gene coding for pyrin. Disease causing mutations in the gene are associated with excessive levels of IL-1. The clinical symptoms of inflammation are mainly in the form of fever and serositis along with laboratory evidence of persi...
متن کاملGenetic screening of FMF in
inherited inflammatory disease that is principally recognized in Jewish, Armenian, Turkish and Arab populations.1 The characteristic intermittent clinical episodes of fever, peritonitis, pleurisy, rashes and arthritis are variable in their pattern, frequency, intensity and age of onset, as is the proportion of FMF patients in different ethnic groups who develop amyloidosis A (AA).2 Since the re...
متن کاملPENDRED\'S SYNDROME REVISITED
Pendred's syndrome is defined as a triad of congenital perceptive hearing loss, goiter, and abnormal perchlorate test. Three brothers with Pendred's syndrome [P.S.] are reported. The oldest brother has hearing loss (he has been deaf and mute since childhood) and has a large goiter. A thyroid scan revealed euthyroid multinodular goiter and a perchlorate test was performed, and reported abno...
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ژورنال
عنوان ژورنال: European Journal of Human Genetics
سال: 2004
ISSN: 1018-4813,1476-5438
DOI: 10.1038/sj.ejhg.5201170