نتایج جستجو برای: h63d

تعداد نتایج: 365  

Journal: :Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas 2003
M M Deguti A M Sipahi L C C Gayotto S A Palácios P L Bittencourt A C Goldberg A A Laudanna F J Carrilho E L R Cançado

The hypothesis of the role of iron overload associated with HFE gene mutations in the pathogenesis of nonalcoholic steatohepatitis (NASH) has been raised in recent years. In the present study, biochemical and histopathological evidence of iron overload and HFE mutations was investigated in NASH patients. Thirty-two NASH patients, 19 females (59%), average 49.2 years, 72% Caucasians, 12% Mulatto...

Journal: :Genetics and molecular research : GMR 2005
Ana L C Martinelli Rui Filho Samantha Cruz Rendrik Franco Marli Tavella Marie Secaf Leandra Ramalho Sergio Zucoloto Sandra Rodrigues Marcos Zago

Hereditary hemochromatosis (HH) is the most common genetic disease among individuals of European descent. Two mutations (845G-->A, C282Y and 187C-->G, H63D) in the hemochromatosis gene (HFE gene) are associated with HH. About 85-90% of patients of northern European descent with HH are C282Y homozygous. The prevalence of HH in the Brazilian population, which has a very high level of racial admix...

Journal: :Revista Brasileira de Hematologia e Hemoterapia 2006

2012
Hossein Sendi Marjan Mehrab-Mohseni

In Western countries, HFE-linked hereditary hemo-chromatosis (HH) is considered to be the most common cause of iron overload. The HFE gene, first identified in 1996, is located on the short arm of chromosome 6. The majority of patients with phenotypic HH are homozy-gous for the C282Y mutation, a major mutation of the HFE gene, whereas compound heterozygosity (C282Y/ H63D) is found in patients w...

Journal: :Gut 2002
P Holmström J Marmur G Eggertsen M Gåfvels P Stål

BACKGROUND AND AIMS The role of the HFE S65C mutation in the development of hepatic iron overload is unknown. The aim of the present study was: (A) to determine the HFE S65C frequency in a Northern European population; and (B) to evaluate whether the presence of the HFE S65C mutation would result in a significant hepatic iron overload. PATIENTS AND METHODS Biochemical iron parameters and HFE ...

2017
Tarun Girotra Abhimanyu Mahajan Christos Sidiropoulos

Hemochromatosis is an autosomal recessive disorder which leads to abnormal iron deposition in the parenchyma of multiple organs causing tissue damage. Accumulation of iron in the brain has been postulated to be associated with several neurodegenerative diseases including Parkinson's disease. The excess iron promotes Parkin and α-synuclein aggregation in the neurons. Excess iron has also been no...

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