(Q35742155)

10 August 2017

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title

Is genetic screening for hemochromatosis worthwhile? (English)

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10 August 2017

author

Cornelia M. van Duijn

series ordinal

3

object named as

Cornelia M van Duijn

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author name string

Omer T Njajou

series ordinal

1

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10 August 2017

Behrooz Z Alizadeh

series ordinal

2

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10 August 2017

publication date

1 January 2004

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European Journal of Epidemiology

10 August 2017

published in

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10 August 2017

volume

19

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10 August 2017

issue

2

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10 August 2017

page(s)

101-108

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Genetic heterogeneity underlies juvenile hemochromatosis phenotype: analysis of three families of northern Greek origin

10 August 2017

cites work

1 reference

12 December 2020

Genetic and clinical description of hemochromatosis probands and heterozygotes: evidence that multiple genes linked to the major histocompatibility complex are responsible for hemochromatosis

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12 December 2020

Screening for hemochromatosis

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12 December 2020

Uncommon mutations and polymorphisms in the hemochromatosis gene

1 reference

12 December 2020

Screening blood donors for hereditary hemochromatosis: decision analysis model comparing genotyping to phenotyping.

1 reference

12 December 2020

Penetrance of 845G--> A (C282Y) HFE hereditary haemochromatosis mutation in the USA.

1 reference

12 December 2020

A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis

1 reference

12 December 2020

Juvenile genetic hemochromatosis is clinically and genetically distinct from the classical HLA-related disorder.

1 reference

12 December 2020

Diagnosis of hemochromatosis.

1 reference

12 December 2020

Iron overload in urban Africans in the 1990s

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12 December 2020

Cost-effectiveness of screening for hereditary hemochromatosis

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12 December 2020

Role of HFE in iron metabolism, hereditary haemochromatosis, anaemia of chronic disease, and secondary iron overload

1 reference

12 December 2020

Hereditary iron overload and African Americans

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12 December 2020

Global prevalence of putative haemochromatosis mutations

1 reference

12 December 2020

Juvenile idiopathic haemochromatosis: a life-threatening disorder presenting as hypogonadotropic hypogonadism

1 reference

12 December 2020

Effects of HFE C282Y and H63D polymorphisms and polygenic background on iron stores in a large community sample of twins

1 reference

12 December 2020

Idiopathic haemochromatosis: An autosomal recessive disease

1 reference

12 December 2020

Mutations in the MHC class I-like candidate gene for hemochromatosis in French patients

1 reference

12 December 2020

Screening for hemochromatosis: phenotyping or genotyping or both?

1 reference

12 December 2020

A population-based study of the effect of the HFE C282Y and H63D mutations on iron metabolism

1 reference

12 December 2020

Idiopathic hemochromatosis. Autosomal recessive disease

1 reference

12 December 2020

Prevalence of Hemochromatosis among 11,065 Presumably Healthy Blood Donors

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12 December 2020

The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22.

1 reference

12 December 2020

A valine deletion of ferroportin 1: a common mutation in hemochromastosis type 4

1 reference

12 December 2020

HFE gene and hereditary hemochromatosis: a HuGE review. Human Genome Epidemiology

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12 December 2020

A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis

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12 December 2020

Screening blood donors for hereditary hemochromatosis: decision analysis model based on a 30-year database

1 reference

12 December 2020

A genotypic study of 217 unrelated probands diagnosed as "genetic hemochromatosis" on "classical" phenotypic criteria

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12 December 2020

Heredity of idiopathic haemochromatosis: a study of 106 families

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12 December 2020

EASL International Consensus Conference on Haemochromatosis

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12 December 2020

Mutation analysis in hereditary hemochromatosis

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12 December 2020

Juvenile hemochromatosis locus maps to chromosome 1q.

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HLA-H mutations in the Ashkenazi Jewish population

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12 December 2020

Prevalence of haemochromatosis amongst asymptomatic Australians

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Haemochromatosis and HLA-H

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12 December 2020

Idiopathic hemochromatosis in young subjects. Clinical, pathological, and chemical findings in four patients

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The genetics of hemochromatosis.

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12 December 2020

Hemochromatosis due to mutations in transferrin receptor 2.

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Practice guideline development task force of the College of American Pathologists. Hereditary hemochromatosis

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Hepatic pathology in relatives of patients with hæmochromatosis

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12 December 2020

Mutations in the hemochromatosis gene (HFE) and stroke

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12 December 2020

Hereditary juvenile haemochromatosis: a genetically heterogeneous life-threatening iron-storage disease

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12 December 2020

Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) gene

1 reference

12 December 2020

Value of hepatic iron measurements in early hemochromatosis and determination of the critical iron level associated with fibrosis

1 reference

12 December 2020

Hemochromatosis and "HLA-H": definite!

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12 December 2020

Crystal structure of the hemochromatosis protein HFE and characterization of its interaction with transferrin receptor

1 reference

12 December 2020

A mutation, in the iron-responsive element of H ferritin mRNA, causing autosomal dominant iron overload

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12 December 2020

Idiopathic hemochromatosis, an iron storage disease. A. Iron metabolism in hemochromatosis

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12 December 2020

Immunohistochemistry of HLA-H, the protein defective in patients with hereditary hemochromatosis, reveals unique pattern of expression in gastrointestinal tract

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12 December 2020

The significance of haemochromatosis gene mutations in the general population: implications for screening

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12 December 2020

Hereditary hemochromatosis in adults without pathogenic mutations in the hemochromatosis gene

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12 December 2020

Hemochromatosis screening in asymptomatic ambulatory men 30 years of age and older

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12 December 2020

Preventing manifestations of hereditary haemochromatosis through population based screening

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12 December 2020

Human genome epidemiology: translating advances in human genetics into population-based data for medicine and public health

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12 December 2020

HFEmutations in patients with hereditary haemochromatosis in Sweden

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12 December 2020

Clinical haemochromatosis in HFE mutation carriers

1 reference

12 December 2020

Clinical haemochromatosis in HFE mutation carriers

1 reference

12 December 2020

The role of hemochromatosis C282Y and H63D gene mutations in type 2 diabetes: findings from the Rotterdam Study and meta-analysis

1 reference

12 December 2020

Juvenile and adult hemochromatosis are distinct genetic disorders

1 reference

12 December 2020

Demonstration by iron overloading study and HLA genotyping of recessive transmission of idiopathic haemochromatosis in two pseudodominant pedigrees (author's transl)

1 reference

12 December 2020

Autosomal dominant reticuloendothelial iron overload associated with a 3-base pair deletion in the ferroportin 1 gene (SLC11A3)

1 reference

12 December 2020

Will Genetics Revolutionize Medicine?

1 reference

12 December 2020

Hereditary hemochromatosis: gene discovery and its implications for population-based screening

1 reference

12 December 2020

Population screening for haemochromatosis: a unifying analysis of published intervention trials

1 reference

12 December 2020

Phenotypic expression of HFE mutations: a French study of 1110 unrelated iron-overloaded patients and relatives

1 reference

12 December 2020

Novel mutation in ferroportin1 is associated with autosomal dominant hemochromatosis

1 reference

12 December 2020

10.1023/B:EJEP.0000017664.96394.B9

Identifiers

DOI

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Dimensions Publication ID

10 August 2017

1017401274

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