Literature DB >> 14444243

Congenital hemolytic disease associated with red cell inclusion bodies, abnormal pigment metabolism and an electrophoretic hemoglobin abnormality.

J L SCOTT, A HAUT, G E CARTWRIGHT, M M WINTROBE.   

Abstract

Entities:  

Keywords:  ANEMIA, HEMOLYTIC/case reports; ERYTHROCYTES; HEMOGLOBIN; PIGMENTS/metabolism

Mesh:

Substances:

Year:  1960        PMID: 14444243

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


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  4 in total

1.  HEREDITARY HEINZ-BODY ANAEMIA, THROMBOCYTOPENIA, AND HAEMOGLOBINOPATHY (HB KOELN) IN A GLASGOW FAMILY.

Authors:  H E HUTCHISON; P H PINKERTON; P WATERS; H LEHMANN; D BEALE; A S DOUGLAS
Journal:  Br Med J       Date:  1964-10-31

2.  THE ROLE OF NONHEMOGLOBIN PROTEINS AND REDUCED GLUTATHIONE IN THE PROTECTION OF HEMOGLOBIN FROM OXIDATION IN VITRO.

Authors:  A S HILL; A HAUT; G E CARTWRIGHT; M M WINTROBE
Journal:  J Clin Invest       Date:  1964-01       Impact factor: 14.808

3.  [Hb frankfurt: a new unstable haemoglobin as the cause of Heinz-body anaemia in a German family].

Authors:  L Nowicki; H Martin
Journal:  Klin Wochenschr       Date:  1971-10-15

4.  Congenital Heinz-body haemolytic anaemia due to haemoglobin Hammersmith.

Authors:  N K Shinton; H P Williams; D C Thursby-Pelham
Journal:  Postgrad Med J       Date:  1969-09       Impact factor: 2.401

  4 in total

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