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Journal Abstract Search

122 related items for PubMed ID: 5862690

  • 1. [Hexokinase deficiency in blood cells in a group of kin with familial panmyelopathy (Fanconi type)].
    Löhr GW, Waller HD, Anschütz F, Knopp A.
    Klin Wochenschr; 1965 Aug 15; 43(16):870-5. PubMed ID: 5862690
    [No Abstract] [Full Text] [Related]

  • 2. Regulation of glycolysis in human red cells.
    Yoshikawa H, Minakami S.
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1968 Aug 15; 89(4):357-75. PubMed ID: 4176832
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  • 3. [Biochemical defects in the blood cells in familial panmyelopathy (Fanconi type)].
    Löhr GW, Waller HD, Anschütz F, Knopp A.
    Humangenetik; 1965 Aug 15; 1(4):383-7. PubMed ID: 5869442
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  • 5. [Cytogenic and biochemical studies of 8 cases of Fanconi's anemia].
    de Grouchy J, de Nava C, Marchand JC, Feingold J, Turleau C.
    Ann Genet; 1972 Mar 15; 15(1):29-40. PubMed ID: 4537612
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  • 11. Studies on leukocyte metabolism. I.
    Minakami S.
    J Biochem; 1968 Jan 15; 63(1):83-8. PubMed ID: 4297629
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  • 12. Mechanism of phosphoryl transfer by hexokinase.
    Rose IA.
    Biochem Biophys Res Commun; 1980 May 30; 94(2):573-8. PubMed ID: 6994724
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  • 13. Inhibition of hexokinase in glucose-6-phosphate dehydrogenase deficient erythrocytes by acetylphenylhydrazine.
    Razin A, Hershko A, Glaser G, Izak G, Mager J.
    Isr J Med Sci; 1965 Jul 30; 1(4):843. PubMed ID: 5856128
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  • 14. Cytogenic observations in congenital familial panmyelopathy (Fanconi's syndrome).
    Coutinho V, Falcao RP, Bottura C.
    Nouv Rev Fr Hematol; 1971 Jul 30; 11(5):781-90. PubMed ID: 4261193
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  • 15. [Comparative biochemical studies of erythrocytes from the blood of the newborn and of adults].
    Witt I, Müller H, Künzer W.
    Klin Wochenschr; 1967 Mar 01; 45(5):262-4. PubMed ID: 4298617
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  • 20. Panmyelopathy with congenital anomalies (Fanconi) in two cousins.
    Hoefnagel D, Sullivan M, McIntyre OR, Gray JA, Storrs RC.
    Helv Paediatr Acta; 1966 Jul 01; 21(3):230-8. PubMed ID: 5990992
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