Literature DB >> 2194598

Haemochromatosis.

T M Cox1.   

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Year:  1990        PMID： 2194598     DOI： 10.1016/0268-960x(90)90030-v

Source DB:  PubMed          Journal:  Blood Rev        ISSN： 0268-960X            Impact factor:   8.250


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  5 in total

1.  Rapid diagnosis of asymptomatic hereditary haemochromatosis by detection of the Cys282Tyr mutation in the HLA-H gene.

Authors:  S Aslam; G R Standen
Journal:  Postgrad Med J       Date:  1997-09       Impact factor: 2.401

2.  Haemochromatosis presenting as congestive cardiac failure.

Authors:  J Porter; N Cary; P Schofield
Journal:  Br Heart J       Date:  1995-01

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

Authors:  K B Raja; D Pountney; A Bomford; R Przemioslo; D Sherman; R J Simpson; R Williams; T J Peters
Journal:  Gut       Date:  1996-05       Impact factor: 23.059

4.  Monocyte-macrophage ferric reductase activity is inhibited by iron and stimulated by cellular differentiation.

Authors:  J Partridge; D F Wallace; K B Raja; J S Dooley; A P Walker
Journal:  Biochem J       Date:  1998-12-15       Impact factor: 3.857

5.  Detection of hereditary haemochromatosis in an HLA-identical pedigree showing discordance between HLA class I genes and the disease locus.

Authors:  I Dokal; D Lord; D Rhodes; G Bydder; T Cox
Journal:  Hum Genet       Date:  1991-12       Impact factor: 4.132
  5 in total

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