Contribution of different HFE genotypes to iron overload disease: a pooled analysis
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M. Khoury | W. Burke | G. Imperatore | R. Baron | S. McDonnell | M. Khoury
[1] P. Adams. Population screening for haemochromatosis , 2000, Gut.
[2] J. J. Pointon,et al. Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results , 1999, Nature Genetics.
[3] R. Ries,et al. Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results , 1999, Nature Genetics.
[4] J. Olynyk,et al. A population-based study of the clinical expression of the hemochromatosis gene. , 1999, The New England journal of medicine.
[5] M. Somerville,et al. An HFE intronic variant promotes misdiagnosis of hereditary hemochromatosis. , 1999, American journal of human genetics.
[6] R. Hegele,et al. Polymorphism in intron 4 of HFE may cause overestimation of C282Y homozygote prevalence in haemochromatosis , 1999, Nature Genetics.
[7] M. Cogswell,et al. Population-based screening for hemochromatosis using phenotypic and DNA testing among employees of health maintenance organizations in Springfield, Missouri. , 1999, The American journal of medicine.
[8] P. Adams. Population screening for hemochromatosis , 1999, Hepatology.
[9] J. L. Le Gall,et al. Phenotypic expression of HFE mutations: a French study of 1110 unrelated iron-overloaded patients and relatives. , 1999, Gastroenterology.
[10] J. Berg,et al. High prevalence of the hemochromatosis-associated Cys282Tyr HFE gene mutation in a healthy Norwegian population in the city of Oslo, and its phenotypic expression. , 1999, Scandinavian journal of gastroenterology.
[11] T. Löffler,et al. HFE codon 63/282 (H63D/C282Y) dimorphism in German patients with genetic hemochromatosis. , 2008, Tissue antigens.
[12] C. Frampton,et al. The significance of haemochromatosis gene mutations in the general population: implications for screening , 1998 .
[13] R. G. Parrish,et al. Hemochromatosis-Associated Mortality in the United States from 1979 to 1992: An Analysis of Multiple-Cause Mortality Data , 1998, Annals of Internal Medicine.
[14] M. Khoury,et al. Iron Overload, Public Health, and Genetics: Evaluating the Evidence for Hemochromatosis Screening , 1998, Annals of Internal Medicine.
[15] M. O'Leary,et al. Prevalence of Hereditary Hemochromatosis in 16 031 Primary Care Patients , 1998, Annals of Internal Medicine.
[16] Mayka Sánchez,et al. Prevalence of the Cys282Tyr and His63Asp HFE gene mutations in Spanish patients with hereditary hemochromatosis and in controls , 1998 .
[17] D. Middleton,et al. High incidence of the Cys 282 Tyr mutation in the HFE gene in the Irish population--implications for haemochromatosis. , 1998, Tissue antigens.
[18] P. Adams. Hemochromatosis: clinical implications of genetic testing. , 1998, CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne.
[19] D. Girelli,et al. Heterogeneity of hemochromatosis in Italy. , 1998, Gastroenterology.
[20] J. Haddow,et al. Hereditary haemochromatosis mutation frequencies in the general population , 1998, Journal of medical screening.
[21] Esin,et al. HFE mutations in patients with hereditary haemochromatosis in Sweden , 1998, Journal of internal medicine.
[22] D. M. Penny,et al. The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[23] R. Oliva,et al. Prevalence of the Cys282Tyr and His63Asp HFE gene mutations in Spanish patients with hereditary hemochromatosis and in controls. , 1998, Journal of hepatology.
[24] J. Kushner,et al. Screening for hemochromatosis: phenotype versus genotype. , 1998, Seminars in hematology.
[25] Roger Williams,et al. A simple genetic test identifies 90% of UK patients with haemochromatosis , 1997, Gut.
[26] W. Sly,et al. Hereditary hemochromatosis: effects of C282Y and H63D mutations on association with beta2-microglobulin, intracellular processing, and cell surface expression of the HFE protein in COS-7 cells. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[27] P. Meier,et al. Identification and functional characterization of the promoter region of the human organic anion transporting polypeptide gene , 1997, Hepatology.
[28] V. David,et al. Clinical and family studies in genetic hemochromatosis: Microsatellite and HFE studies in five atypical families , 1997, Hepatology.
[29] B. Bacon. Diagnosis and management of hemochromatosis. , 1997, Gastroenterology.
[30] R. Wolff,et al. The Hemochromatosis Founder Mutation in HLA-H Disrupts β2-Microglobulin Interaction and Cell Surface Expression* , 1997, The Journal of Biological Chemistry.
[31] B. Bacon,et al. Hereditary hemochromatosis: presentation and diagnosis in the 1990s. , 1997, The American journal of gastroenterology.
[32] J. Barton,et al. Genetic and clinical description of hemochromatosis probands and heterozygotes: evidence that multiple genes linked to the major histocompatibility complex are responsible for hemochromatosis. , 1997, Blood cells, molecules & diseases.
[33] J. Bodmer,et al. Putting a hold on ‘HLA–H’ , 1997, Nature Genetics.
[34] C. Férec,et al. Putting a hold on ‘HLA–H’ , 1997, Nature Genetics.
[35] J. Vinel,et al. Mutations in the MHC class I-like candidate gene for hemochromatosis in French patients , 1997, Immunogenetics.
[36] J. Haddow,et al. Population Screening for Haemochromatosis: A Unifying Analysis of Published Intervention Trials , 1996, Journal of medical screening.
[37] C. P. Morris,et al. Haemochromatosis and HLA–H , 1996, Nature Genetics.
[38] P. Fergelot,et al. Haemochromatosis and HLA–H , 1996, Nature Genetics.
[39] C. Venditti,et al. Mutation analysis in hereditary hemochromatosis. , 1996, Blood cells, molecules & diseases.
[40] M. C. Ellis,et al. A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis , 1996, Nature Genetics.
[41] J. Gregor,et al. Screening blood donors for hereditary hemochromatosis: decision analysis model based on a 30-year database. , 1995, Gastroenterology.
[42] J. L. Simons,et al. Hemochromatosis screening in asymptomatic ambulatory men 30 years of age and older. , 1995, The American journal of medicine.
[43] M. Burritt,et al. Screening for hemochromatosis: a cost-effectiveness study based on 12,258 patients. , 1994, Gastroenterology.
[44] B. Lin,et al. Prevalence of hemochromatosis in a random sample of asymptomatic men. , 1986, Australian and New Zealand journal of medicine.