Screening for hemochromatosis.

Suppr

超能文献

作者信息

Edwards C Q, Kushner J P

机构信息

Department of Medicine, University of Utah College of Medicine, Salt Lake City 84132.

出版信息

N Engl J Med. 1993 Jun 3;328(22):1616-20. doi: 10.1056/NEJM199306033282208.

DOI:10.1056/NEJM199306033282208

PMID:8110209

Abstract

摘要

相似文献

Screening for hemochromatosis.

N Engl J Med. 1993 Jun 3;328(22):1616-20. doi: 10.1056/NEJM199306033282208.

The molecular basis for the association between HLA-A3 and idiopathic haemochromatosis.

Exp Clin Immunogenet. 1984;1(1):25-30.

The frequency of hemochromatosis-associated alleles is increased in British patients with sporadic porphyria cutanea tarda.

Hepatology. 1997 Jan;25(1):159-61. doi: 10.1002/hep.510250129.

[Idiopathic hemochromatosis in an HLA-A3 heterozygote].

Ugeskr Laeger. 1988 Aug 22;150(34):2040-1.

[Correlation of HLA antigens and idiopathic hemochromatosis in Hungary].

Orv Hetil. 1991 Feb 24;132(8):409-10, 413-5.

Disorders of inadequate iron.

Hosp Pract (Off Ed). 1991 Apr;26 Suppl 3:25-9. doi: 10.1080/21548331.1991.11704281.

Laboratory testing for iron status.

Hosp Pract (Off Ed). 1991 Apr;26 Suppl 3:17-24. doi: 10.1080/21548331.1991.11704280.

Iron overload in three generations of a family with hemoglobin Olympia.

Gastroenterology. 1984 Sep;87(3):695-702.

Association between a 10 kb Pvu II restriction fragment of genomic DNA with the hemochromatosis gene.

Exp Clin Immunogenet. 1986;3(4):219-23.

Primary hemochromatosis in childhood.

Pediatrics. 1987 Oct;80(4):549-54.

引用本文的文献

Health Economic Evaluations of Hemochromatosis Screening and Treatment: A Systematic Review.

Pharmacoecon Open. 2024 Mar;8(2):147-170. doi: 10.1007/s41669-023-00463-6. Epub 2024 Jan 27.

Genotype, Ferritin Levels and Transferrin Saturation in Patients with Suspected Hereditary Hemochromatosis.

Genes (Basel). 2021 Jul 28;12(8):1162. doi: 10.3390/genes12081162.

Hereditary hemochromatosis.

Autops Case Rep. 2015 Mar 30;5(1):7-10. doi: 10.4322/acr.2014.043. eCollection 2015 Jan-Mar.

Infiltrative Cardiomyopathies.

Clin Med Insights Cardiol. 2015 Jul 8;9(Suppl 2):29-38. doi: 10.4137/CMC.S19706. eCollection 2015.

[Molecular genetic analysis and clinical aspects of patients with hereditary hemochromatosis].

Orthopade. 2014 Aug;43(8):772-9. doi: 10.1007/s00132-014-2318-y.

Transferrin saturation ratio and risk of total and cardiovascular mortality in the general population.

QJM. 2014 Aug;107(8):623-33. doi: 10.1093/qjmed/hcu045. Epub 2014 Mar 5.

Transferrin saturation and hospital length of stay and mortality in Medicare beneficiaries.

J Am Geriatr Soc. 2013 Jan;61(1):132-6. doi: 10.1111/jgs.12044. Epub 2012 Dec 3.

Iron homeostasis and eye disease.

Biochim Biophys Acta. 2009 Jul;1790(7):637-49. doi: 10.1016/j.bbagen.2008.11.001. Epub 2008 Nov 14.

Targeted screening for genetic haemochromatosis: a combined phenotype/genotype approach.

J Clin Pathol. 2006 May;59(5):501-4. doi: 10.1136/jcp.2005.031898.

Iron loading and morbidity among relatives of HFE C282Y homozygotes identified either by population genetic testing or presenting as patients.

Gut. 2006 Apr;55(4):554-62. doi: 10.1136/gut.2005.070342. Epub 2005 Sep 20.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验

相似文献

Screening for hemochromatosis.

N Engl J Med. 1993 Jun 3;328(22):1616-20. doi: 10.1056/NEJM199306033282208.

The molecular basis for the association between HLA-A3 and idiopathic haemochromatosis.

Exp Clin Immunogenet. 1984;1(1):25-30.

The frequency of hemochromatosis-associated alleles is increased in British patients with sporadic porphyria cutanea tarda.

Hepatology. 1997 Jan;25(1):159-61. doi: 10.1002/hep.510250129.

[Idiopathic hemochromatosis in an HLA-A3 heterozygote].

Ugeskr Laeger. 1988 Aug 22;150(34):2040-1.

[Correlation of HLA antigens and idiopathic hemochromatosis in Hungary].

Orv Hetil. 1991 Feb 24;132(8):409-10, 413-5.

Disorders of inadequate iron.

Hosp Pract (Off Ed). 1991 Apr;26 Suppl 3:25-9. doi: 10.1080/21548331.1991.11704281.

Laboratory testing for iron status.

Hosp Pract (Off Ed). 1991 Apr;26 Suppl 3:17-24. doi: 10.1080/21548331.1991.11704280.

Iron overload in three generations of a family with hemoglobin Olympia.

Gastroenterology. 1984 Sep;87(3):695-702.

Association between a 10 kb Pvu II restriction fragment of genomic DNA with the hemochromatosis gene.

Exp Clin Immunogenet. 1986;3(4):219-23.

Primary hemochromatosis in childhood.

Pediatrics. 1987 Oct;80(4):549-54.

引用本文的文献

Health Economic Evaluations of Hemochromatosis Screening and Treatment: A Systematic Review.

Pharmacoecon Open. 2024 Mar;8(2):147-170. doi: 10.1007/s41669-023-00463-6. Epub 2024 Jan 27.

Genotype, Ferritin Levels and Transferrin Saturation in Patients with Suspected Hereditary Hemochromatosis.

Genes (Basel). 2021 Jul 28;12(8):1162. doi: 10.3390/genes12081162.

Hereditary hemochromatosis.

Autops Case Rep. 2015 Mar 30;5(1):7-10. doi: 10.4322/acr.2014.043. eCollection 2015 Jan-Mar.

Infiltrative Cardiomyopathies.

Clin Med Insights Cardiol. 2015 Jul 8;9(Suppl 2):29-38. doi: 10.4137/CMC.S19706. eCollection 2015.

[Molecular genetic analysis and clinical aspects of patients with hereditary hemochromatosis].

Orthopade. 2014 Aug;43(8):772-9. doi: 10.1007/s00132-014-2318-y.

Transferrin saturation ratio and risk of total and cardiovascular mortality in the general population.

QJM. 2014 Aug;107(8):623-33. doi: 10.1093/qjmed/hcu045. Epub 2014 Mar 5.

Transferrin saturation and hospital length of stay and mortality in Medicare beneficiaries.

J Am Geriatr Soc. 2013 Jan;61(1):132-6. doi: 10.1111/jgs.12044. Epub 2012 Dec 3.

Iron homeostasis and eye disease.

Biochim Biophys Acta. 2009 Jul;1790(7):637-49. doi: 10.1016/j.bbagen.2008.11.001. Epub 2008 Nov 14.

Targeted screening for genetic haemochromatosis: a combined phenotype/genotype approach.

J Clin Pathol. 2006 May;59(5):501-4. doi: 10.1136/jcp.2005.031898.

Iron loading and morbidity among relatives of HFE C282Y homozygotes identified either by population genetic testing or presenting as patients.

Gut. 2006 Apr;55(4):554-62. doi: 10.1136/gut.2005.070342. Epub 2005 Sep 20.