These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

255 related items for PubMed ID: 8043936

  • 1. Congenital dyserythropoietic anaemia type II (HEMPAS) and its molecular basis.
    Fukuda MN.
    Baillieres Clin Haematol; 1993 Jun; 6(2):493-511. PubMed ID: 8043936
    [Abstract] [Full Text] [Related]

  • 2. HEMPAS disease: genetic defect of glycosylation.
    Fukuda MN.
    Glycobiology; 1990 Sep; 1(1):9-15. PubMed ID: 2136385
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. HEMPAS. Hereditary erythroblastic multinuclearity with positive acidified serum lysis test.
    Fukuda MN.
    Biochim Biophys Acta; 1999 Oct 08; 1455(2-3):231-9. PubMed ID: 10571015
    [Abstract] [Full Text] [Related]

  • 5. Congenital dyserythropoietic anemias.
    Marks PW, Mitus AJ.
    Am J Hematol; 1996 Jan 08; 51(1):55-63. PubMed ID: 8571938
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. 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 08; 110(4):998-1001. PubMed ID: 11054095
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. Primary defect of congenital dyserythropoietic anemia type II. Failure in glycosylation of erythrocyte lactosaminoglycan proteins caused by lowered N-acetylglucosaminyltransferase II.
    Fukuda MN, Dell A, Scartezzini P.
    J Biol Chem; 1987 May 25; 262(15):7195-206. PubMed ID: 2953718
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Structural and functional consequences of an N-glycosylation mutation (HEMPAS) affecting human erythrocyte membrane glycoproteins.
    Kameh H, Landolt-Marticorena C, Charuk JH, Schachter H, Reithmeier RA.
    Biochem Cell Biol; 1998 May 25; 76(5):823-35. PubMed ID: 10353717
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Incompletely processed N-glycans of serum glycoproteins in congenital dyserythropoietic anaemia type II (HEMPAS).
    Fukuda MN, Gaetani GF, Izzo P, Scartezzini P, Dell A.
    Br J Haematol; 1992 Dec 25; 82(4):745-52. PubMed ID: 1482662
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Congenital dyserythropoietic anemia, type II with SEC23B exon 12 c.1385 A → G mutation, and pseudo-Gaucher cells in two siblings.
    Sharma P, Das R, Bansal D, Trehan A.
    Hematology; 2015 Mar 25; 20(2):104-7. PubMed ID: 24801240
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 13.