HFE C282Y/H63D compound heterozygotes are at low risk of hemochromatosis-related morbidity.
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Evidence for the high importance of co-morbid factors in HFE C282Y/H63D patients cared by phlebotomies: results from an observational prospective studyEffect of C282Y genotype on self-reported musculoskeletal complications in hereditary hemochromatosisPathophysiological consequences and benefits of HFE mutations: 20 years of research.Effects of C282Y, H63D, and S65C HFE gene mutations, diet, and life-style factors on iron status in a general Mediterranean population from Tarragona, SpainHFE gene mutations increase the risk of coronary heart disease in women.HFE Cys282Tyr homozygotes with serum ferritin concentrations below 1000 microg/L are at low risk of hemochromatosis.Hepatic but not brain iron is rapidly chelated by deferasirox in aceruloplasminemia due to a novel gene mutation.EMQN best practice guidelines for the molecular genetic diagnosis of hereditary hemochromatosis (HH).Molecular diagnosis of hemochromatosis.Natural history of HFE simple heterozygosity for C282Y and H63D: a prospective 12-year study.Detection of metallic cobalt and chromium liver deposition following failed hip replacement using T2* and R2 magnetic resonanceTelomere length and elevated iron: the influence of phenotype and HFE genotypeHFE C282Y homozygotes are at increased risk of breast and colorectal cancerThe evolutionary adaptation of the C282Y mutation to culture and climate during the European Neolithic.Molecular diagnosis of genetic iron-overload disorders.Diagnosis and treatment of hereditary hemochromatosis: an update.HFE p.C282Y homozygosity predisposes to rapid serum ferritin rise after menopause: A genotype-stratified cohort study of hemochromatosis in Australian women.ACG Clinical Guideline: Evaluation of Abnormal Liver Chemistries.To tell or not to tell - what to do about p.C282Y heterozygotes identified by HFE screening.Causes of iron overload in blood donors - a clinical study.Reduction of Skeletal Muscle Power in Adolescent Males Carrying H63D Mutation in the HFE Gene.Identification of new BMP6 pro-peptide mutations in patients with iron overload.Hereditary hemochromatosis is characterized by a clinically definable arthropathy that correlates with iron load
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P2860
HFE C282Y/H63D compound heterozygotes are at low risk of hemochromatosis-related morbidity.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on July 2009
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
HFE C282Y/H63D compound hetero ...... chromatosis-related morbidity.
@en
HFE C282Y/H63D compound hetero ...... chromatosis-related morbidity.
@nl
type
label
HFE C282Y/H63D compound hetero ...... chromatosis-related morbidity.
@en
HFE C282Y/H63D compound hetero ...... chromatosis-related morbidity.
@nl
prefLabel
HFE C282Y/H63D compound hetero ...... chromatosis-related morbidity.
@en
HFE C282Y/H63D compound hetero ...... chromatosis-related morbidity.
@nl
P2093
P2860
P50
P356
P1433
P1476
HFE C282Y/H63D compound hetero ...... chromatosis-related morbidity.
@en
P2093
Christine E McLaren
Clare C Constantine
Dorota M Gertig
Gregory W Dalton
HealthIron Study Investigators
Lawrie W Powell
Martin B Delatycki
Nadine A Bertalli
P2860
P304
P356
10.1002/HEP.22972
P407
P50
P577
2009-07-01T00:00:00Z