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Hereditary haemochromatosis.

作者信息

Edwards C Q, Dadone M M, Skolnick M H, Kushner J P

出版信息

Clin Haematol. 1982 Jun;11(2):411-35.

PMID:7042159

Abstract

摘要

相似文献

Hereditary haemochromatosis.

Clin Haematol. 1982 Jun;11(2):411-35.

Relationship between genotype, assessed by HLA typing, and phenotypic expression of iron status markers in families of 29 probands with hereditary haemochromatosis.

Dan Med Bull. 1994 Jun;41(3):366-70.

[Iron metabolism in hereditary hemochromatosis].

Vrach Delo. 1989 Apr(4):65-9.

Hemochromatosis in a family.

Am Fam Physician. 1987 Jun;35(6):145-50.

[Idiopathic hemochromatosis].

Minerva Med. 1985 Mar 31;76(13):627-34.

[Hereditary hemochromatosis].

Rev Gastroenterol Peru. 2003 Oct-Dec;23(4):302-6.

Inheritance of hemochromatosis: linkage to HLA.

Trans Assoc Am Physicians. 1978;91:273-81.

[Hereditary hemochromatosis].

Klin Med (Mosk). 1988 Mar;66(3):136-42.

Carbohydrate intolerance in idiopathic haemochromatosis and cirrhosis of the liver.

Q J Med. 1973 Oct;42(168):733-49.

HLA-A3 and serum iron. A study in an Irish control population.

Tissue Antigens. 1983 May;21(5):402-4.

引用本文的文献

Hepatobiliary disorders in celiac disease: an update.

Int J Hepatol. 2011;2011:438184. doi: 10.4061/2011/438184. Epub 2010 Nov 14.

Association between C282Y and H63D mutations of the HFE gene with hepatocellular carcinoma in European populations: a meta-analysis.

J Exp Clin Cancer Res. 2010 Mar 2;29(1):18. doi: 10.1186/1756-9966-29-18.

High prevalence of abnormal glucose homeostasis secondary to decreased insulin secretion in individuals with hereditary haemochromatosis.

Diabetologia. 2006 Jul;49(7):1661-9. doi: 10.1007/s00125-006-0200-0. Epub 2006 Mar 15.

Duodenal mucosal reductase in wild-type and Hfe knockout mice on iron adequate, iron deficient, and iron rich feeding.

Gut. 2003 Apr;52(4):510-3. doi: 10.1136/gut.52.4.510.

HLA-A and -B alleles and haplotypes in hemochromatosis probands with HFE C282Y homozygosity in central Alabama.

BMC Med Genet. 2002 Oct 7;3:9. doi: 10.1186/1471-2350-3-9.

Mouse strain differences determine severity of iron accumulation in Hfe knockout model of hereditary hemochromatosis.

Proc Natl Acad Sci U S A. 2001 Feb 27;98(5):2707-11. doi: 10.1073/pnas.051630898.

Syncope and inducible ventricular fibrillation in a woman with hemochromatosis.

J Interv Card Electrophysiol. 1999 Oct;3(3):225-9. doi: 10.1023/a:1009891406964.

Homogeneous multiplex genotyping of hemochromatosis mutations with fluorescent hybridization probes.

Am J Pathol. 1998 Oct;153(4):1055-61. doi: 10.1016/S0002-9440(10)65650-7.

Haplotype analysis of hemochromatosis: evaluation of different linkage-disequilibrium approaches and evolution of disease chromosomes.

Am J Hum Genet. 1997 Jun;60(6):1439-47. doi: 10.1086/515466.

A duodenal mucosal abnormality in the reduction of Fe(III) in patients with genetic haemochromatosis.

Gut. 1996 May;38(5):765-9. doi: 10.1136/gut.38.5.765.

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Hereditary haemochromatosis.

作者信息

Edwards C Q, Dadone M M, Skolnick M H, Kushner J P

出版信息

Clin Haematol. 1982 Jun;11(2):411-35.

PMID:7042159

Abstract

摘要

相似文献

Hereditary haemochromatosis.

Clin Haematol. 1982 Jun;11(2):411-35.

Relationship between genotype, assessed by HLA typing, and phenotypic expression of iron status markers in families of 29 probands with hereditary haemochromatosis.

Dan Med Bull. 1994 Jun;41(3):366-70.

[Iron metabolism in hereditary hemochromatosis].

Vrach Delo. 1989 Apr(4):65-9.

Hemochromatosis in a family.

Am Fam Physician. 1987 Jun;35(6):145-50.

[Idiopathic hemochromatosis].

Minerva Med. 1985 Mar 31;76(13):627-34.

[Hereditary hemochromatosis].

Rev Gastroenterol Peru. 2003 Oct-Dec;23(4):302-6.

Inheritance of hemochromatosis: linkage to HLA.

Trans Assoc Am Physicians. 1978;91:273-81.

[Hereditary hemochromatosis].

Klin Med (Mosk). 1988 Mar;66(3):136-42.

Carbohydrate intolerance in idiopathic haemochromatosis and cirrhosis of the liver.

Q J Med. 1973 Oct;42(168):733-49.

HLA-A3 and serum iron. A study in an Irish control population.

Tissue Antigens. 1983 May;21(5):402-4.

引用本文的文献

Hepatobiliary disorders in celiac disease: an update.

Int J Hepatol. 2011;2011:438184. doi: 10.4061/2011/438184. Epub 2010 Nov 14.

Association between C282Y and H63D mutations of the HFE gene with hepatocellular carcinoma in European populations: a meta-analysis.

J Exp Clin Cancer Res. 2010 Mar 2;29(1):18. doi: 10.1186/1756-9966-29-18.

High prevalence of abnormal glucose homeostasis secondary to decreased insulin secretion in individuals with hereditary haemochromatosis.

Diabetologia. 2006 Jul;49(7):1661-9. doi: 10.1007/s00125-006-0200-0. Epub 2006 Mar 15.

Duodenal mucosal reductase in wild-type and Hfe knockout mice on iron adequate, iron deficient, and iron rich feeding.

Gut. 2003 Apr;52(4):510-3. doi: 10.1136/gut.52.4.510.

HLA-A and -B alleles and haplotypes in hemochromatosis probands with HFE C282Y homozygosity in central Alabama.

BMC Med Genet. 2002 Oct 7;3:9. doi: 10.1186/1471-2350-3-9.

Mouse strain differences determine severity of iron accumulation in Hfe knockout model of hereditary hemochromatosis.

Proc Natl Acad Sci U S A. 2001 Feb 27;98(5):2707-11. doi: 10.1073/pnas.051630898.

Syncope and inducible ventricular fibrillation in a woman with hemochromatosis.

J Interv Card Electrophysiol. 1999 Oct;3(3):225-9. doi: 10.1023/a:1009891406964.

Homogeneous multiplex genotyping of hemochromatosis mutations with fluorescent hybridization probes.

Am J Pathol. 1998 Oct;153(4):1055-61. doi: 10.1016/S0002-9440(10)65650-7.

Haplotype analysis of hemochromatosis: evaluation of different linkage-disequilibrium approaches and evolution of disease chromosomes.

Am J Hum Genet. 1997 Jun;60(6):1439-47. doi: 10.1086/515466.

A duodenal mucosal abnormality in the reduction of Fe(III) in patients with genetic haemochromatosis.

Gut. 1996 May;38(5):765-9. doi: 10.1136/gut.38.5.765.