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Journal Abstract Search

253 related items for PubMed ID: 4809302

  • 1. Glucose phosphate isomerase deficiency with congenital nonspherocytic hemolytic anemia: a new variant (type Nordhorn). I. Clinical and genetic studies.
    Schröter W, Koch HH, Wonneberger B, Kalinowsky W, Arnold A, Blume KG, Hüther W.
    Pediatr Res; 1974 Jan; 8(1):18-25. PubMed ID: 4809302
    [No Abstract] [Full Text] [Related]

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  • 3. Glucosephosphate-isomerase (GPI) deficiency: GPI elyria.
    Beutler E, Sigalove WH, Muir WA, Matsumoto F, West C.
    Ann Intern Med; 1974 Jun; 80(6):730-2. PubMed ID: 4832160
    [No Abstract] [Full Text] [Related]

  • 4. Fine structure of the spleen and liver in glucosephosphate isomerase (GPI) deficiency hereditary nonspherocytic hemolytic anemia. Selective reticulocyte destruction as a mechanism of hemolysis.
    Matsumoto N, Ishihara T, Oda E, Miwa S, Nakashima K.
    Nihon Ketsueki Gakkai Zasshi; 1973 Feb; 36(1):46-54. PubMed ID: 4738991
    [No Abstract] [Full Text] [Related]

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  • 6. Glucosephosphate isomerase (GPI) deficiency hereditary nonspherocytic hemolytic anemia. Report of the first case found in Japanese.
    Miwa S, Nakashima Y, Oda S, Oda E, Matsumoto N.
    Nihon Ketsueki Gakkai Zasshi; 1973 Feb; 36(1):65-9. PubMed ID: 4738992
    [No Abstract] [Full Text] [Related]

  • 7. Glucosephosphate isomerase (GPI) deficiency hereditary nonspherocytic hemolytic anemia. Report of the second case found in Japanese.
    Miwa S, Nakashima K, Oda S, Matsumoto N, Ogawa H.
    Nihon Ketsueki Gakkai Zasshi; 1973 Feb; 36(1):70-3. PubMed ID: 4738993
    [No Abstract] [Full Text] [Related]

  • 8. Erythrocyte and leukocyte phosphoglycerate kinase deficiency with neurologic disease.
    Konrad PN, McCarthy DJ, Mauer AM, Valentine WN, Paglia DE.
    J Pediatr; 1973 Mar; 82(3):456-60. PubMed ID: 4698932
    [No Abstract] [Full Text] [Related]

  • 9. [Clinical and biochemical studies of glucosephosphate isomerase of normal human erythrocytes and in glucosephosphate isomerase deficiency].
    Arnold H, Blume KG, Busch D, Lenkeit U, Löhr GW, Lübs E.
    Klin Wochenschr; 1970 Nov 01; 48(21):1299-308. PubMed ID: 5519415
    [No Abstract] [Full Text] [Related]

  • 10. Hereditary deficiency of glucosephosphate isomerase as a cause of nonspherocytic hemolytic anemia.
    Löhr GW, Arnold H, Blume KG, Engelhardt R, Beutler E.
    Blut; 1973 Jun 01; 26(6):393-8. PubMed ID: 4715119
    [No Abstract] [Full Text] [Related]

  • 11. Occurrence of defective hexosephosphate isomerization in human erythrocytes and leukocytes.
    Paglia DE, Holland P, Baughan MA, Valentine WN.
    N Engl J Med; 1969 Jan 09; 280(2):66-71. PubMed ID: 5782480
    [No Abstract] [Full Text] [Related]

  • 12. [Glucose phosphate isomerase type Recklinghausen: a new enzyme variant with haemolytic anaemia (author's transl)].
    Arnold H, Engelhardt R, Löhr GW, Jacobi H, Liebold I.
    Klin Wochenschr; 1973 Dec 15; 51(24):1198-204. PubMed ID: 4789327
    [No Abstract] [Full Text] [Related]

  • 13. Pyruvate kinase deficiency.
    Tanaka KR, Paglia DE.
    Semin Hematol; 1971 Oct 15; 8(4):367-96. PubMed ID: 4942588
    [No Abstract] [Full Text] [Related]

  • 14. Deficiencies associated with Embden-Meyerhof pathway and other metabolic pathways.
    Valentine WN.
    Semin Hematol; 1971 Oct 15; 8(4):348-66. PubMed ID: 4256808
    [No Abstract] [Full Text] [Related]

  • 15.
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  • 16. The inherited defects of erythrocyte metabolism.
    Fornaini G, Bossu M.
    Ital J Biochem; 1969 Oct 15; 18(4):185-326. PubMed ID: 4243574
    [No Abstract] [Full Text] [Related]

  • 17. [Adenosine triphosphatase (ATP-ase) deficiency in a family with nonspherocytic hemolytic anemia].
    Cohn J, Hanel HK, Harvald B.
    Nord Med; 1971 Dec 16; 86(50):1540. PubMed ID: 4257475
    [No Abstract] [Full Text] [Related]

  • 18. [Haemolytic anaemia due to congenital deffect in phosphohexoseisomerase. Report of a new variant (PHI-Barcelona) with stomatocytosis and increased osmotic fragility (author's transl)].
    Vives-Corrons JL, Carrera A, Triginer J, Kahn A, Rozman C.
    Sangre (Barc); 1975 Dec 16; 20(2):197-206. PubMed ID: 1145398
    [No Abstract] [Full Text] [Related]

  • 19. -Glutamyl-cysteine synthetase deficiency. A cause of hereditary hemolytic anemia.
    Konrad PN, Richards F, Valentine WN, Paglia DE.
    N Engl J Med; 1972 Mar 16; 286(11):557-61. PubMed ID: 5058793
    [No Abstract] [Full Text] [Related]

  • 20. Clinical heterogeneity of erythrocyte pyruvate kinase deficiency. Evidence of an impaired utilization of ATP in a clinically severe form.
    Schröter W.
    Helv Paediatr Acta; 1972 Nov 16; 27(5):471-88. PubMed ID: 4640902
    [No Abstract] [Full Text] [Related]

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