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Journal Abstract Search

132 related items for PubMed ID: 6025012

  • 1. Compensated hereditary haemolytic disease resulting from an unstable haemoglobin fraction.
    Raik E, Hunter EG, Lindsay DA.
    Med J Aust; 1967 May 13; 1(19):955-8. PubMed ID: 6025012
    [No Abstract] [Full Text] [Related]

  • 2. [Chronic haemolytic anemia due to a defect of glucose-6-phosphate dehydrogenase (G6PD) in a Lorraine family. Demonstration of a new type of the enzyme: Gd(-) Nancy].
    Streiff F, Vigneron C.
    Nouv Rev Fr Hematol; 1971 May 13; 11(2):279-90. PubMed ID: 4252680
    [No Abstract] [Full Text] [Related]

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  • 4. Unstable haemoglobin Köln disease in members of a Malay family.
    Eng LL, Lopez CG, Eapen JS, Eravelly J, Wiltshire BG, Lehmann H.
    J Med Genet; 1972 Sep 13; 9(3):340-3. PubMed ID: 5079107
    [No Abstract] [Full Text] [Related]

  • 5. [Metabolic abnormality in erthyrocytes with atypical pyruvate kinase and potassium deficiency].
    Grieger M, Günther I, Jacobasch G, Buss D, Gerth C.
    Haematologia (Budap); 1972 Sep 13; 6(4):379-94. PubMed ID: 4362236
    [No Abstract] [Full Text] [Related]

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  • 7. [Hereditary non-spherocytic hemolytic anemia caused by glucosephosphate isomerase deficiency: 1. case observed in Switzerland].
    Müller E, Marti HR, Bach J, Micheli JL, Gasser C.
    Schweiz Med Wochenschr; 1974 Sep 28; 104(39):1379-81. PubMed ID: 4419288
    [No Abstract] [Full Text] [Related]

  • 8. Adenosine-triphosphatase deficiency in a family with non-spherocytic haemolytic anaemia.
    Hanel HK, Cohn J, Harvald B.
    Hum Hered; 1971 Sep 28; 21(4):313-9. PubMed ID: 4257922
    [No Abstract] [Full Text] [Related]

  • 9. [Hemolytic anemias caused by genetic disorders in human red cells].
    Benöhr HC.
    Arztl Forsch; 1970 Jan 10; 24(1):19-29. PubMed ID: 4398687
    [No Abstract] [Full Text] [Related]

  • 10. Hereditary nonspherocytic hemolytic disease associated with an altered phospholipid composition of the erythrocytes.
    Jaffé ER, Gottfried EL.
    J Clin Invest; 1968 Jun 10; 47(6):1375-88. PubMed ID: 5653215
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  • 12. [Diagnosis of hemolytic anemia with unstable hemoglobin].
    Sakalová A, Hrubisko M.
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1980 Jun 10; 107(4):641-7. PubMed ID: 6162731
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  • 13. Inherited erythrocyte pyruvate kinase deficiency: Studies on 15 members of two related families.
    Dachà M, Canestrari F, Bossù M, Ferrini PL, Fornaini G.
    Acta Haematol; 1977 Jun 10; 57(1):37-46. PubMed ID: 190844
    [Abstract] [Full Text] [Related]

  • 14. Glucosephosphate isomerase (GPI) deficiency mutations associated with hereditary nonspherocytic hemolytic anemia (HNSHA).
    Beutler E, West C, Britton HA, Harris J, Forman L.
    Blood Cells Mol Dis; 1997 Dec 10; 23(3):402-9. PubMed ID: 9446754
    [Abstract] [Full Text] [Related]

  • 15. [Oxygenation curves in enzymopathic hemolytic anemias].
    Rotrekl B, Prokopová M.
    Acta Univ Palacki Olomuc Fac Med; 1984 Dec 10; 106():123-31. PubMed ID: 6242617
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  • 18. 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 10; 36(1):70-3. PubMed ID: 4738993
    [No Abstract] [Full Text] [Related]

  • 19. [Double heterozygous predisposition for Hb P ( 2 2 117 His--Arg ) and the classic -thalassemia in an Aargau-family].
    Rosenmund A, Winterhalter KH, Haber J, Marti HR.
    Schweiz Med Wochenschr; 1972 Nov 04; 102(44):1624-6. PubMed ID: 4645055
    [No Abstract] [Full Text] [Related]

  • 20. [Congenital enzymopenic hemolytic anemias].
    Moser K.
    Wien Klin Wochenschr; 1969 Apr 04; 81(14):249-58. PubMed ID: 5784529
    [No Abstract] [Full Text] [Related]

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