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Journal Abstract Search

164 related items for PubMed ID: 5423587

  • 21. Hemoglobin Köln disease occurring as a fresh mutation: erythrocyte metabolism and survival.
    Miller DR, Weed RI, Stamatoyannopoulos G, Yoshida A.
    Blood; 1971 Dec; 38(6):715-29. PubMed ID: 4942314
    [No Abstract] [Full Text] [Related]

  • 22. A new variant of hereditary hemolytic anemia with stomatocytosis and erythrocyte cation abnormality.
    Miller DR, Rickles FR, Lichtman MA, La Celle PL, Bates J, Weed RI.
    Blood; 1971 Aug; 38(2):184-204. PubMed ID: 5559828
    [No Abstract] [Full Text] [Related]

  • 23. Three families with unstable hemoglobinopathies (Köln, Olmsted and Santa Ana) causing hemolytic anemia with inclusion bodies and pigmenturia.
    Fairbanks VF, Opfell RW, Burgert EO.
    Am J Med; 1969 Mar; 46(3):344-59. PubMed ID: 5780360
    [No Abstract] [Full Text] [Related]

  • 24. Köln haemoglobinopathy. Further data and a comparison with other hereditary Heinz body anaemias.
    Jones RV, Grimes AJ, Carrell RW, Lehmann H.
    Br J Haematol; 1967 May; 13(3):394-408. PubMed ID: 6067323
    [No Abstract] [Full Text] [Related]

  • 25. [Methods for the diagnosis of hemolytic anemias specified by unstable pathological hemoglobins].
    Didkovskiĭ NA, Filippova AV, Idel'son LI.
    Lab Delo; 1971 May; 3():154-8. PubMed ID: 4108708
    [No Abstract] [Full Text] [Related]

  • 26. Hereditary non-spherocytic haemolytic anaemia with post-splenectomy inclusion bodies and pigmenturia caused by an unstable haemoglobin Santa Ana-beta-88 (F4) leucine--proline.
    Opfell RW, Lorkin PA, Lehmann H.
    J Med Genet; 1968 Dec; 5(4):292-7. PubMed ID: 5713642
    [No Abstract] [Full Text] [Related]

  • 27. An approach to the diagnosis of haemolytic anaemia. II.
    Kimber RJ.
    Med J Aust; 1974 Oct 12; 2(15):566-8. PubMed ID: 4431372
    [No Abstract] [Full Text] [Related]

  • 28. Adaptive mechanism for abnormal membrane fluidity in congenital red cell membrane lipid abnormalities.
    Yawata Y, Sugihara T, Hashimoto M, Kanzaki A, Ikeda A, Nozawa Y.
    Biomed Biochim Acta; 1987 Oct 12; 46(2-3):S26-30. PubMed ID: 3593305
    [No Abstract] [Full Text] [Related]

  • 29. The diverse forms of the erythrocyte pyruvate kinase deficiency states.
    Zarkowsky HS.
    Med Times; 1969 Aug 12; 97(8):177-82. PubMed ID: 5795609
    [No Abstract] [Full Text] [Related]

  • 30. [Major acanthocytosis following splenectomy for hemolytic anemia. Study of erythrocytic lipids. Rise in plasma lysolecithin levels].
    Gouffier E, Garnier M, Turpin F, Paraf A.
    Ann Med Interne (Paris); 1973 Dec 12; 124(12):915-9. PubMed ID: 4791386
    [No Abstract] [Full Text] [Related]

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  • 32. [ABNORMAL HEMOGLOBIN AND FAMILIAL HEMOLYTIC ANEMIA WITH ERYTHROCYTIC INCLUSIONS AND BLACK URINES].
    GOUDEMAND M, BISERTE G, HABAY D, VOISIN D.
    Nouv Rev Fr Hematol; 1964 Dec 12; 4():487-504. PubMed ID: 14188997
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  • 36. Clinical studies and physiological properties of Hopkins-2 haemoglobin.
    Charache S, Ostertag W, von Ehrenstein G.
    Nat New Biol; 1972 May 17; 237(72):88-90. PubMed ID: 4503918
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  • 40. [Case of chronic myeloleukemia with hemolytic anemia caused by pathological unstable hemoglobin].
    Idel'son LI, Didkovskiĭ NA, Volkova MA, Fleĭshman EV, Troitskaia OV.
    Probl Gematol Pereliv Krovi; 1971 Feb 17; 16(2):29-32. PubMed ID: 5280307
    [No Abstract] [Full Text] [Related]

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