about
Infiltrative CardiomyopathiesMultiple organ dysfunction in a 33-year-old woman due to hereditary hemochromatosis.Pumping iron.Homozygosity for the predominant Cys282Tyr mutation and absence of disease expression in hereditary haemochromatosisThe haemochromatosis gene: a global perspective and implications for the Asia-Pacific region.Transferrin saturation ratio and risk of total and cardiovascular mortality in the general population.Inherited liver diseases in adultsElevated serum transferrin saturation and mortalityTransferrin saturation, dietary iron intake, and risk of cancer.The significance of haemochromatosis gene mutations in the general population: implications for screening.Screening for genetic haemochromatosis in blood samples with raised alanine aminotransferase.Reflective testing: how useful is the practice of adding on tests by laboratory clinicians?Underdiagnosis of hereditary haemochromatosis: lack of presentation or penetration?Transferrin saturation and hospital length of stay and mortality in Medicare beneficiariesIron loading and morbidity among relatives of HFE C282Y homozygotes identified either by population genetic testing or presenting as patients.Targeted screening for genetic haemochromatosis: a combined phenotype/genotype approachComparison of histological and biochemical hepatic iron indexes in the diagnosis of genetic haemochromatosisIron homeostasis and eye disease.Iron metabolism and diagnosis of iron overload disorders.The health effects of vitamin C supplementation: a review.Etiologies, consequences, and treatment of iron overload.Review article: the screening, diagnosis and optimal management of haemochromatosis.Hemochromatosis: the genetic disorder of the twenty-first century.Kupffer cell staining by an HFE-specific monoclonal antibody: implications for hereditary haemochromatosis.Preventing manifestations of hereditary haemochromatosis through population based screening.Mixture models in haematology: a series of case studies.Hereditary hemochromatosis. Preventing chronic effects of this underdiagnosed disorder.Hereditary haemochromatosis as an immunological disease.HFE based re-evaluation of heterozygous hemochromatosis.Hemochromatosis probands as blood donors.The effect of HFE mutations on serum ferritin and transferrin saturation in the Jersey population.Population screening for haemochromatosis: expectations based on a study of relatives of symptomatic probands.Diagnosing hemochromatosis.Hereditary hemochromatosis
P2860
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P2860
description
1993 nî lūn-bûn
@nan
1993 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1993 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
name
Screening for hemochromatosis.
@ast
Screening for hemochromatosis.
@en
Screening for hemochromatosis.
@nl
type
label
Screening for hemochromatosis.
@ast
Screening for hemochromatosis.
@en
Screening for hemochromatosis.
@nl
prefLabel
Screening for hemochromatosis.
@ast
Screening for hemochromatosis.
@en
Screening for hemochromatosis.
@nl
P1476
Screening for hemochromatosis.
@en
P2093
Edwards CQ
Kushner JP
P304
P356
10.1056/NEJM199306033282208
P407
P577
1993-06-01T00:00:00Z