نتایج جستجو برای: hfe gene

تعداد نتایج: 1142155  

Journal: :Heart 2004
I R Gunn F K Maxwell D Gaffney A D McMahon C J Packard

OBJECTIVES To measure the frequency of genotypes of the HFE (haemochromatosis) gene in patients recruited to the west of Scotland coronary prevention study (WOSCOPS), and relate them to the subsequent occurrence of coronary clinical events. DESIGN Nested case-control study, drawing samples of DNA from the biological bank of a cohort study. PATIENTS Men aged 45-64 years in 1989, with moderat...

Journal: :The Journal of Nutrition 2011

Journal: :Revista Brasileira de Hematologia e Hemoterapia 2006

Journal: :American Journal of Epidemiology 2001

Journal: :Journal of Evidence Based Medicine and Healthcare 2019

2011
Ola H. Gebril Nagwa A. Meguid

BACKGROUND Autism is among the commonest neurodevelopmental childhood disorders worldwide; its aetiology is still unknown. Iron metabolism alteration in the central nervous system is recently implicated as a risk factor for several neurodegenerative disorders. Haemochromatosis HFE gene polymorphisms (p.H63D and p.C282Y) have shown significant association with several neurological diseases. Some...

2014
Pascale Carayon Anping Xie Sarah Kianfar

BACKGROUND Human factors and ergonomics (HFE) approaches to patient safety have addressed five different domains: usability of technology; human error and its role in patient safety; the role of healthcare worker performance in patient safety; system resilience; and HFE systems approaches to patient safety. METHODS A review of various HFE approaches to patient safety and studies on HFE interv...

2009
Paulo Lisboa Bittencourt Maria Lúcia Carnevale Marin Cláudia Alves Couto Eduardo Luiz Rachid Cançado Flair José Carrilho Anna Carla Goldberg

BACKGROUND Approximately one-half of Brazilian patients with hereditary hemochromatosis (HH) are neither homozygous for the C282Y mutation nor compound heterozygous for the H63D and C282Y mutations that are associated with HH in Caucasians. Other mutations have been described in the HFE gene as well as in genes involved in iron metabolism, such as transferrin receptor 2 (TfR2) and ferroportin 1...

Journal: :BMC Neurology 2006
Rita J Guerreiro Jose M Bras Isabel Santana Cristina Januario Beatriz Santiago Ana S Morgadinho Maria H Ribeiro John Hardy Andrew Singleton Catarina Oliveira

BACKGROUND Pathological brain iron deposition has been implicated as a source of neurotoxic reactive oxygen species in Alzheimer (AD) and Parkinson diseases (PD). Iron metabolism is associated with the gene hemochromatosis (HFE Human genome nomenclature committee ID:4886), and mutations in HFE are a cause of the iron mismetabolism disease, hemochromatosis. Several reports have tested the associ...

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