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Journal Abstract Search

134 related items for PubMed ID: 7055536

  • 21. Congenital dyserythropoietic anaemia type II (HEMPAS): characterization of aberrant intracellular organelles by immunogold electron microscopy.
    Fukuda MN, Klier G, Scartezzini P.
    Br J Haematol; 1987 Sep; 67(1):95-101. PubMed ID: 3663523
    [Abstract] [Full Text] [Related]

  • 22. A case of congenital dyserythropoietic anaemia with stomatocytosis, reduced bands 7 and 8 and normal cation content.
    Olivieri O, Girelli D, Vettore L, Balercia G, Corrocher R.
    Br J Haematol; 1992 Feb; 80(2):258-60. PubMed ID: 1550788
    [No Abstract] [Full Text] [Related]

  • 23. Glycophorin A in two patients with congenital dyserythropoietic anemia type I and type II is partly unglycosylated.
    Zdebska E, Adamczyk-Popławska M, Kościelak J.
    Acta Biochim Pol; 2000 Feb; 47(3):773-9. PubMed ID: 11310976
    [Abstract] [Full Text] [Related]

  • 24. Gel electrophoresis of the human erythrocyte membrane proteins: aberrant patterns in hematological and non-hematological diseases.
    Anselstetter V.
    Blut; 1978 Mar 15; 36(3):135-44. PubMed ID: 638265
    [No Abstract] [Full Text] [Related]

  • 25. A variant of the congenital dyserythropoietic anaemia type II with structural abnormalities in the granulocytic series.
    Vermylen C, Scheiff JM, Rodhain J, Ninane J, Cornu G.
    Eur J Pediatr; 1986 Aug 15; 145(3):232-5. PubMed ID: 3769984
    [Abstract] [Full Text] [Related]

  • 26. A new congenital dyserythropoietic anaemia.
    Ohisalo JJ, Viitala J, Lintula R, Ruutu T.
    Br J Haematol; 1988 Jan 15; 68(1):111-4. PubMed ID: 3345287
    [Abstract] [Full Text] [Related]

  • 27. Unclassified type of congenital dyserythropoietic anaemia (CDA) with prominent peripheral erythroblastosis.
    Bird AR, Karabus CD, Hartley PS.
    Br J Haematol; 1986 Aug 15; 63(4):797-8. PubMed ID: 3730300
    [No Abstract] [Full Text] [Related]

  • 28. Congenital dyserythropoietic anaemia type I: absence of clonal expression in the nuclear abnormalities of cultured erythroblasts.
    Vainchenker W, Guichard J, Bouguet J, Breton-Gorius J.
    Br J Haematol; 1980 Sep 15; 46(1):33-7. PubMed ID: 7426450
    [Abstract] [Full Text] [Related]

  • 29. Short report: erythrocyte membranes from a patient with congenital dyserythropoietic anaemia type I (CDA-I) show identical, although less pronounced, glycoconjugate abnormalities to those from patients with CDA-II (HEMPAS).
    Zdebska E, Woźniewicz B, Adamowicz-Salach A, Kościelak J.
    Br J Haematol; 2000 Sep 15; 110(4):998-1001. PubMed ID: 11054095
    [Abstract] [Full Text] [Related]

  • 30.
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  • 31. [Case report of congenital dyserythropoietic anemia (CDA) type I].
    Atono Y, Ogata H, Nohno R, Sakisaka S, Masiko N, Satoh K, Nakashima F, Tanikawa K, Ebata H, Murakami M.
    Rinsho Ketsueki; 1987 Aug 15; 28(8):1414-8. PubMed ID: 3430753
    [No Abstract] [Full Text] [Related]

  • 32. [Immunologic characteristics and changes in the protein structure of the erythrocyte membrane in dyserythropoietic anemia, type 2].
    Idel'son LI, Vygovskaia IaI, Koĭfman MM, Savchenko VG, Zherdeva LV.
    Probl Gematol Pereliv Krovi; 1978 Jan 15; 23(1):48-52. PubMed ID: 628667
    [No Abstract] [Full Text] [Related]

  • 33. Congenital dyserythropoietic anaemia in children: report of three cases from Kuwait.
    Zaki M, Hassanein AA, Daoud AS, al Saleh Q.
    Ann Trop Paediatr; 1989 Sep 15; 9(3):161-4. PubMed ID: 2475061
    [Abstract] [Full Text] [Related]

  • 34. 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 Sep 15; 70(4):243-9. PubMed ID: 6414210
    [Abstract] [Full Text] [Related]

  • 35. [Morphological studies of erythrocytes in congenital dyserythropoietic anemia type II].
    Koehler M, Schmidt-Riese L, Brandeis WE.
    Acta Haematol Pol; 1990 Sep 15; 21(2):144-52. PubMed ID: 2131714
    [Abstract] [Full Text] [Related]

  • 36. Flow-cytometric analysis of erythrocytes and reticulocytes in congenital dyserythropoietic anaemia type II (CDA II): value in differential diagnosis with hereditary spherocytosis.
    Danise P, Amendola G, Nobili B, Perrotta S, Miraglia Del Giudice E, Matarese SM, Iolascon A, Brugnara C.
    Clin Lab Haematol; 2001 Feb 15; 23(1):7-13. PubMed ID: 11422224
    [Abstract] [Full Text] [Related]

  • 37. Congenital dyserythropoietic anemia type I: a freeze-fracture and thin section electron microscopic study.
    Hiraoka A, Kanayama Y, Yonezawa T, Kitani T, Tarui S, Hashimoto PH.
    Blut; 1983 Jun 15; 46(6):329-38. PubMed ID: 6850102
    [Abstract] [Full Text] [Related]

  • 38. Ineffective erythropoiesis underlies the clinical heterogeneity of congenital dyserythropoietic anemia type II (CDA II).
    Kostaridou S, Polychronopoulou S, Premetis E, Papassotiriou I, Stamoulakatou A, Haidas S.
    Pediatr Int; 2004 Jun 15; 46(3):274-9. PubMed ID: 15151542
    [Abstract] [Full Text] [Related]

  • 39. Unclassified type of congenital dyserythropoietic anaemia (CDA) with prominent peripheral erythroblastosis.
    Bethlenfalvay NC, Hadnagy C, Heimpel H.
    Br J Haematol; 1985 Jul 15; 60(3):541-50. PubMed ID: 4015990
    [Abstract] [Full Text] [Related]

  • 40. [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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