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Journal Abstract Search

166 related items for PubMed ID: 3345287

  • 1. A new congenital dyserythropoietic anaemia.
    Ohisalo JJ, Viitala J, Lintula R, Ruutu T.
    Br J Haematol; 1988 Jan; 68(1):111-4. PubMed ID: 3345287
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  • 3. A case of congenital dyserythropoietic anemia type II (HEMPAS).
    Moriwaki Y, Matsui K, Fujioka H, Iwahashi N, Seno T, Tamura S, Yamamoto T, Amuro Y, Hada T, Higashino K.
    Nihon Ketsueki Gakkai Zasshi; 1985 Feb; 48(1):29-36. PubMed ID: 4003011
    [No Abstract] [Full Text] [Related]

  • 4. Unclassified type of congenital dyserythropoietic anaemia (CDA) with prominent peripheral erythroblastosis.
    Bethlenfalvay NC, Hadnagy C, Heimpel H.
    Br J Haematol; 1985 Jul; 60(3):541-50. PubMed ID: 4015990
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  • 5. Congenital dyserytropoietic anaemia, type II (HEMPAS) in three siblings.
    Chrobák L, Radochová D, Smetana K, Matĕja F, Kout M, Polák J, Dítĕ P, Pribroský J, Dvorácková I.
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1980 Jul; 107(4):628-40. PubMed ID: 6162730
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  • 6. [Type I congenital dyserythropoietic anemia presenting in the neonatal period].
    Madero L, Muñoz A, Fernández-Fuertes I, Villa E, Escribano L.
    Sangre (Barc); 1987 Jul; 32(4):495-501. PubMed ID: 3660188
    [No Abstract] [Full Text] [Related]

  • 7. Transmission and scanning electron microscopy study on congenital dyserythropoietic anemia type I.
    Conde E, Mazo E, Baro J, Lafarga M, Cuadrado MA, Recio M, Zubizarreta A.
    Acta Haematol; 1983 Jul; 70(4):243-9. PubMed ID: 6414210
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  • 8. Congenital dyserythropoietic anaemia.
    Prasher N, Prasher BS.
    J Assoc Physicians India; 1989 Jul; 37(7):467-8. PubMed ID: 2613664
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  • 11. Congenital dyserythropoietic anaemia type II (HEMPAS): a family study.
    McCann SR, Firth R, Murray N, Temperley IJ.
    J Clin Pathol; 1980 Dec; 33(12):1197-201. PubMed ID: 7451666
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  • 12. [Erythroid colonies derived from BFU-E from the bone marrow in a patient with type I congenital dyserythropoietic anemia].
    Florensa L, Woessner S, Almarcha J, Pardo Peret P, Lafuente R, Vilá RM.
    Sangre (Barc); 1990 Jun; 35(3):219-21. PubMed ID: 2396168
    [Abstract] [Full Text] [Related]

  • 13. Variant congenital dyserythropoietic anaemia with ringed sideroblasts.
    Brien WF, Mant MJ, Etches WS.
    Clin Lab Haematol; 1985 Jun; 7(3):231-7. PubMed ID: 4075738
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  • 15. [Congenital dyserythropoietic anemia morphologically type I with a positive HEMPAS phenomenon].
    Bergua Burgués JM, Navarro D, González J, Doblaré E.
    Sangre (Barc); 1998 Feb; 43(1):59-61. PubMed ID: 9577182
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  • 16. [Congenital dyserythropoietic anemia type II. Report of a new case and literature review].
    Simón Marco E, Monferrer Guardiola R, Baño Aracil M, Cacho Sobrino F, Gozalbo Gasco T, Branchadel Igual T, Vera-Roman JM.
    Rev Clin Esp; 1998 Feb; 170(3-4):149-52. PubMed ID: 6647930
    [No Abstract] [Full Text] [Related]

  • 17. Congenital dyserythropoietic anaemia (CDA) with severe gout, rare Kell phenotype and erythrocyte, granulocyte and platelet membrane reduplication: a new variant of CDA type II.
    Lowenthal RM, Marsden KA, Dewar CL, Thompson GR.
    Br J Haematol; 1980 Feb; 44(2):211-20. PubMed ID: 7378299
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  • 18. [Congenital dyserythropoietic anemia, type II. Personal case].
    Gandullia E, Veneziano G.
    Minerva Pediatr; 1981 May 15; 33(9):423-8. PubMed ID: 7254161
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  • 19. Defect in glycosylation of erythrocyte membrane proteins in congenital dyserythropoietic anaemia type II (HEMPAS).
    Fukuda MN, Papayannopoulou T, Gordon-Smith EC, Rochant H, Testa U.
    Br J Haematol; 1984 Jan 15; 56(1):55-68. PubMed ID: 6538436
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  • 20. [Abnormalities of the erythrocyte membrane ultrastructure and the membrane proteins in a patient with HEMPAS, alpha thalassemia and complicated diabetes].
    Li JY, Xu YQ, Huang ZX, Zhou H, Wan SD.
    Zhonghua Nei Ke Za Zhi; 2004 Jun 15; 43(6):426-8. PubMed ID: 15312436
    [Abstract] [Full Text] [Related]

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