Literature DB >> 4640902

Clinical heterogeneity of erythrocyte pyruvate kinase deficiency. Evidence of an impaired utilization of ATP in a clinically severe form.

W Schröter.   

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Year:  1972        PMID： 4640902

Source DB:  PubMed          Journal:  Helv Paediatr Acta        ISSN： 0018-022X


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  7 in total

Review 1.  Advances in hereditary red cell enzyme anomalies.

Authors:  A Kahn; J C Kaplan; J C Dreyfus
Journal:  Hum Genet       Date:  1979       Impact factor: 4.132

2.  Role of the spleen in congenital stomatocytosis associated with high sodium-low potassium erythrocytes.

Authors:  W Schröter; K Ungefehr; W Tillmann
Journal:  Klin Wochenschr       Date:  1981-02-16

3.  Search for a relationship between molecular anomalies of the mutant erythrocyte pyruvate kinase variants and their pathological expression.

Authors:  A Kahn; J Marie; J L Vives-Corrons; P Maigret; A Najman
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

4.  Pyruvate kinase-catalyzed ATP-formation in human red blood cell membranes.

Authors:  W Schröter; W Tillmann; G Söndgen
Journal:  Blut       Date:  1978-07-14

5.  Membrane-localized pyruvate kinase of red blood cells in hemolytic anemia associated with pyruvate kinase deficiency.

Authors:  W Schröter; W Tillmann
Journal:  Klin Wochenschr       Date:  1975-12-01

6.  Molecular mechanism of erythrocyte pyruvate kinase deficiency.

Authors:  A Kahn; J Marie; C Galand; P Boivin
Journal:  Humangenetik       Date:  1975-10-07

Review 7.  [Enzyme deficiencies in glycolysis and nucleotide metabolism of red blood cells in nonspherocytic hemolytic anemia (author's transl)].

Authors:  H D Waller; H C Benöhr
Journal:  Klin Wochenschr       Date:  1976-09-01
  7 in total

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