نتایج جستجو برای: favism

تعداد نتایج: 143  

2012

Background: Glucose-6-Phosphate dehydrogenase (G6PD) deficiency is an Xlinked recessive disorder expressed mostly in males. Prevalence of G6PD deficiency varies in different parts of the world’s according to ethnic variation. The incidence varies among different countries in the world and surveys report rates of less than 1% to 35%. The prevalence of G6PD deficiency in the Arab world has variou...

In order to explore the nature of glucose-6-phosphate dehydrogenase (G6PD) deficiency in one of the coastal provinces of the Caspian Sea (Mazandaran) in Iran, we have analysed the G6PD gene in 74 unrelated G6PD-deficient males (2-6 year children) with a history of Favism, by using PCR and subsequent digestion by appropriate restriction enzymes, looking for the presence of certain known mutation...

Journal: :iranian journal of public health 0
d.d.farhud ; h.sadighi ; p.amirshahi ; f. sh. tavakkoli

the quantitative measurements of gc(p37, c=20); (‘p(p=4o, c=20); lgg(p=67. c= 50);iga(p- 67,c: :50)and 1gm (p=67,(’=50) were carried out on patients with favism and healthy individuals, both school boys, from the caspian sea litlorals. comparison of’ these groups revealed differences, significant for gc (x2 =10.177), lgm(x2 9.6151), lga(x2 9.2821), highly significant for igg (x2=47.1228), and n...

Journal: :Blood 2007
Nanne M Kamerbeek Rob van Zwieten Martin de Boer Gert Morren Herma Vuil Natalja Bannink Carsten Lincke Koert M Dolman Katja Becker R Heiner Schirmer Stephan Gromer Dirk Roos

Hereditary glutathione reductase (GR) deficiency was found in only 2 cases when testing more than 15 000 blood samples. We have investigated the blood cells of 2 patients (1a and 1b) in a previously described family suffering from favism and cataract and of a novel patient (2) presenting with severe neonatal jaundice. Red blood cells and leukocytes of the patients in family 1 did not contain an...

Journal: :The Journal of clinical investigation 1959
B RAMOT A SZEINBERG A ADAM C SHEBA D GAFNI

A hereditary abnormality of the erythrocytes was described in Negroes sensitive to primaquine (1). A similar or identical defect has been detected in the erythrocytes of a considerable proportion of non-Ashkenazic Jews susceptible to favism and sensitive to various drugs (2-4). The primary defect of these erythrocytes is probably the markedly decreased activity of glucose6-phosphate dehydrogena...

2016
Carlo Giuseppe Rizzello Ilario Losito Laura Facchini Kati Katina Francesco Palmisano Marco Gobbetti Rossana Coda

In spite of its positive repercussions on nutrition and environment, faba bean still remains an underutilized crop due to the presence of some undesired compounds. The pyrimidine glycosides vicine and convicine are precursors of the aglycones divicine and isouramil, the main factors of favism, a genetic condition which may lead to severe hemolysis after faba bean ingestion. The reduction of vic...

2017
Er-Meng Yu Hao-Fang Zhang Zhi-Fei Li Guang-Jun Wang Hong-Kai Wu Jun Xie De-Guang Yu Yun Xia Kai Zhang Wang-Bo Gong

Fish muscle growth is important for the rapidly developing global aquaculture industry, particularly with respect to production and quality. Changes in muscle fibre size are accomplished by altering the balance between protein synthesis and proteolysis. However, our understanding regarding the effects of different protein sources on fish muscle proteins is still limited. Here we report on the p...

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