نتایج جستجو برای: hereditary enzymopathy

تعداد نتایج: 84335  

Journal: :Oncology 2007
Karen Greco

About 6% of colorectal cancers are caused by genetic mutations associated with hereditary colorectal cancer syndromes. The most common hereditary cancer syndromes nurses are likely to encounter include hereditary nonpolyposis colon cancer or Lynch syndrome, familial adenomatous polyposis, attenuated familial adenomatous polyposis, and MYH polyposis. Current colorectal cancer recommendations for...

Journal: :iranian rehabilitation journal 0
younes lotfi department of audiology, university of social welfare and rehabilitation sciences, tehran, iran. saeideh mehrkian department of audiology, university of social welfare and rehabilitation sciences, tehran, iran.

consanguineous marriage is strongly favored in many large human populations. in the most parts of south asia, consanguineous marriage account for 20%  to over 50% of the general population. the effect of consanguinity on hereditary deafness has been well studied and documented. many authors have suggested that approximately one half  of sensory neural hearing loss in children can be attributed ...

M. Eshaghi Gordji

Let A be a Banach algebra. A is called ideally amenable if for every closed ideal I of A, the first cohomology group of A with coefficients in I* is trivial. We investigate the closed ideals I for which H1 (A,I* )={0}, whenever A is weakly amenable or a biflat Banach algebra. Also we give some hereditary properties of ideal amenability.

Journal: :Journal of Korean Medical Science 1992
M. K. Kim C. H. Yang S. H. Kang C. J. Lyu K. Y. Kim

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common hereditary enzyme disorder and more than 200 million people have a deficiency in this enzyme. It is a globally important cause of neonatal jaundice and causes life-threatening hemolytic crisis in childhood. At later ages, certain drugs such as antimalarials, and fava beans cause hemolysis among G6PD deficiency patients. The ...

1999
I. Reiten M. Van den Bergh

In this paper we classify noetherian hereditary abelian categories satisfying Serre duality in the sense of Bondal and Kapranov. As a consequence we obtain a classification of saturated noetherian hereditary categories. As a side result we show that when our hereditary categories have no nonzero projectives or injectives, then the Serre duality property is equivalent to the existence of almost ...

Journal: :basic and clinical neuroscience 0
behnam zamanian iranian national center for addiction studies, tehran university of medical sciences ali goodarzi institute for cognitive sciences studies (icss) hamed ekhtiari no. 669, south karegar ave, tehran, 13366-16357, iran. tel: +9821-55421177, +98912-1885898 email: [email protected]

a b s t r a c t “addiction” is a multifaceted complicated disorder with many interrelated causes, as well as environmental and genetic features. several hereditary variables that have an effect on these features might work in together to influence vulnerability and the extent of being an addict. molecular re-sequencing of the latest and formerly researched genes holds a crucial place with regar...

Journal: :Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico 2011
Begoña Graña Enrique Lastra Gemma Llort Joan Brunet Dolores Isla

Research in genetics has facilitated the identification of highly penetrant genes responsible for a large number of diseases. In the oncology field, genetic counselling and gene testing are focused on the two most common syndromes in familial cancer: hereditary breast and ovarian cancer syndrome (HBOC) and hereditary non-polyposis colorectal cancer or Lynch syndrome (LS). The objective of this ...

Leila Tahmasebi, Mehran Karimi , Narges Rezaei , Sezaneh Haghpanah ,

Abstract Background: Hereditary red cell enzyme disorders are a group of Non-immune/Spherocytic Hemolytic Anemia, although these disorders are rare and they have not public health problems, the detection of these defects could help to physician in treatment and differential diagnosis. This study evaluated 5 enzymopathies in patients with Hereditary Non –immune/Spherocytic Hemolyti...

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