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Journal Abstract Search

187 related items for PubMed ID: 5028468

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. [Hereditary elliptocytosis and pyruvate kinase deficiency of the erythrocytes].
    Neumann E, Schwarzmeier J, Honetz H.
    Wien Klin Wochenschr; 1972 Nov 03; 84(44):712-5. PubMed ID: 5085467
    [No Abstract] [Full Text] [Related]

  • 23. [Anaemia, iron index status and acute phase proteins in malaria (Abidjan, Côte d'Ivoire)].
    Ahiboh H, Oga AS, Yapi HF, Kouakou G, Boua KD, Edjeme N, Monnet D.
    Bull Soc Pathol Exot; 2008 Feb 03; 101(1):25-8. PubMed ID: 18432003
    [Abstract] [Full Text] [Related]

  • 24.
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  • 25. Hereditary haemolytic ovalocytosis with defective erythropoiesis.
    Torlontano G, Fioritoni G, Salvati AM.
    Br J Haematol; 1979 Nov 03; 43(3):435-41. PubMed ID: 497120
    [Abstract] [Full Text] [Related]

  • 26. Ovalocytosis and malaria.
    Fleming AF.
    Lancet; 1988 Oct 08; 2(8615):857. PubMed ID: 2902306
    [No Abstract] [Full Text] [Related]

  • 27.
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  • 28.
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  • 29. [Malaria in pregnant women. Presentation of 2 cases and review of the literature].
    Flici O, Tadjerouni A, Leroy F, Teys JP, Hubinont PO.
    J Gynecol Obstet Biol Reprod (Paris); 1982 Oct 08; 11(8):981-90. PubMed ID: 6763616
    [No Abstract] [Full Text] [Related]

  • 30.
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  • 31.
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  • 32.
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  • 33. Pyknocytosis in a neonate: an unusual presentation of hereditary elliptocytosis.
    Carpentieri U, Gustavson LP, Haggard ME.
    Clin Pediatr (Phila); 1977 Jan 08; 16(1):76-8. PubMed ID: 830464
    [No Abstract] [Full Text] [Related]

  • 34. Alpha128 Arg-->Ser (CGT-->AGT) spectrin mutation associated with severe neonatal elliptopoikilocytosis in Spain.
    Corrons JL, Pujades A, Alvarez R, Estella J, Dhermy D.
    Haematologica; 2001 May 08; 86(5):537-8. PubMed ID: 11410419
    [No Abstract] [Full Text] [Related]

  • 35. Hereditary pyropoikilocytosis and elliptocytosis: clinical, laboratory, and ultrastructural features in infants and children.
    Prchal JT, Castleberry RP, Parmley RT, Crist WM, Malluh A.
    Pediatr Res; 1982 Jun 08; 16(6):484-9. PubMed ID: 7099765
    [Abstract] [Full Text] [Related]

  • 36. [A case of acquired hemolytic icterus in a family affected with constitutional elliptocytosis].
    DRUEZ G.
    Acta Clin Belg; 1952 Jun 08; 7(5):497-505. PubMed ID: 13016125
    [No Abstract] [Full Text] [Related]

  • 37. Hereditary elliptocytosis with hemolytic anemia complicating pregnancy.
    Breckenridge RL, Riggs JA.
    Am J Obstet Gynecol; 1968 Jul 15; 101(6):861-2. PubMed ID: 5660991
    [No Abstract] [Full Text] [Related]

  • 38. Coombs'-positive hemolytic disease in malaria.
    Adner MM, Altstatt LB, Conrad ME.
    Ann Intern Med; 1968 Jan 15; 68(1):33-8. PubMed ID: 4229630
    [No Abstract] [Full Text] [Related]

  • 39. The life span of the elliptocyte; hereditary elliptocytosis and its relationship to other familial hemolytic diseases.
    MOTULSKY AG, SINGER K, CROSBY WH, SMITH V.
    Blood; 1954 Jan 15; 9(1):57-72. PubMed ID: 13115472
    [No Abstract] [Full Text] [Related]

  • 40. Case report. Hereditary elliptocytosis with glucose-6-phosphate dehyrogenase deficiency and haemolytic anaemia.
    RATNESAR VC.
    Ghana Med J; 1963 Mar 15; 2():29-33. PubMed ID: 13973269
    [No Abstract] [Full Text] [Related]

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