Literature DB >> 14242501

HEREDITARY HEMOLYTIC ANEMIA WITH TRIOSEPHOSPHATE ISOMERASE DEFICIENCY.

A S SCHNEIDER, W N VALENTINE, M HATTORI, H L HEINS.   

Abstract

Entities:  

Keywords:  ALDOLASE; ANEMIA, HEMOLYTIC, CONGENITAL; CARBOHYDRATE METABOLISM, INBORN ERRORS; ERYTHROCYTES; GENETICS, HUMAN; GLUCOSEPHOSPHATE DEHYDROGENASE; GLUTATHIONE REDUCTASE; GLYCERALDEHYDEPHOSPHATE DEHYDROGENASE; HEXOKINASE; HYDRO-LYASES; INFANT; ISOMERASES; LACTATE DEHYDROGENASE; LEUKOCYTES; PENTOSEPHOSPHATES; PHOSPHATES; PHOSPHOFRUCTOKINASE; PHOSPHOGLUCOMUTASE; PHOSPHOGLUCONATE DEHYDROGENASE; PHOSPHOGLYCERATE KINASE; PYRUVATE KINASE

Mesh:

Substances:

Year:  1965        PMID: 14242501     DOI: 10.1056/NEJM196502042720503

Source DB:  PubMed          Journal:  N Engl J Med        ISSN: 0028-4793            Impact factor:   91.245


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8.  Lead poisoning: association with hemolytic anemia, basophilic stippling, erythrocyte pyrimidine 5'-nucleotidase deficiency, and intraerythrocytic accumulation of pyrimidines.

Authors:  W N Valentine; D E Paglia; K Fink; G Madokoro
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9.  Hereditary triose phosphate isomerase deficiency: seven new homozygous cases.

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