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Journal Abstract Search


616 related items for PubMed ID: 10498555

  • 21. Deficiency of glycosyl-phosphatidylinositol-linked membrane glycoproteins of leukocytes in paroxysmal nocturnal hemoglobinuria, description of a new diagnostic cytofluorometric assay.
    van der Schoot CE, Huizinga TW, van 't Veer-Korthof ET, Wijmans R, Pinkster J, von dem Borne AE.
    Blood; 1990 Nov 01; 76(9):1853-9. PubMed ID: 2145990
    [Abstract] [Full Text] [Related]

  • 22. Circulating PIG-A mutant T lymphocytes in healthy adults and patients with bone marrow failure syndromes.
    Ware RE, Pickens CV, DeCastro CM, Howard TA.
    Exp Hematol; 2001 Dec 01; 29(12):1403-9. PubMed ID: 11750098
    [Abstract] [Full Text] [Related]

  • 23. Paroxysmal nocturnal hemoglobinuria in children.
    van den Heuvel-Eibrink MM.
    Paediatr Drugs; 2007 Dec 01; 9(1):11-6. PubMed ID: 17291133
    [Abstract] [Full Text] [Related]

  • 24. Flow cytometry screening for paroxysmal nocturnal hemoglobinuria: A single-center experience in Saudi Arabia.
    AlGhasham N, Abulkhair Y, Khalil S.
    Cytometry B Clin Cytom; 2015 Dec 01; 88(6):389-94. PubMed ID: 26296648
    [Abstract] [Full Text] [Related]

  • 25. The novel monoclonal antibody By114 helps detect the early emergence of a paroxysmal nocturnal hemoglobinuria clone in aplastic anemia.
    Tooze JA, Saso R, Marsh JC, Papadopoulos A, Pulford K, Gordon-Smith EC.
    Exp Hematol; 1995 Dec 01; 23(14):1484-91. PubMed ID: 8542935
    [Abstract] [Full Text] [Related]

  • 26. Presentation clinical, haematological and immunophenotypic features of 1081 patients with GPI-deficient (paroxysmal nocturnal haemoglobinuria) cells detected by flow cytometry.
    Richards SJ, Dickinson AJ, Cullen MJ, Griffin M, Munir T, McKinley C, Mitchell LD, Newton DJ, Arnold L, Hill A, Hillmen P.
    Br J Haematol; 2020 Jun 01; 189(5):954-966. PubMed ID: 32103498
    [Abstract] [Full Text] [Related]

  • 27. The PIG-A mutation and absence of glycosylphosphatidylinositol-linked proteins do not confer resistance to apoptosis in paroxysmal nocturnal hemoglobinuria.
    Ware RE, Nishimura J, Moody MA, Smith C, Rosse WF, Howard TA.
    Blood; 1998 Oct 01; 92(7):2541-50. PubMed ID: 9746796
    [Abstract] [Full Text] [Related]

  • 28. Aplastic anemia and paroxysmal nocturnal hemoglobinuria: search for a pathogenetic link.
    Griscelli-Bennaceur A, Gluckman E, Scrobohaci ML, Jonveaux P, Vu T, Bazarbachi A, Carosella ED, Sigaux F, Socié G.
    Blood; 1995 Mar 01; 85(5):1354-63. PubMed ID: 7858265
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  • 29. ICCS/ESCCA consensus guidelines to detect GPI-deficient cells in paroxysmal nocturnal hemoglobinuria (PNH) and related disorders part 1 - clinical utility.
    Dezern AE, Borowitz MJ.
    Cytometry B Clin Cytom; 2018 Jan 01; 94(1):16-22. PubMed ID: 29236352
    [Abstract] [Full Text] [Related]

  • 30. Paroxysmal nocturnal hemoglobinuria (membrane defect, pathogenesis, aplastic anemia, diagnosis).
    Chrobák L.
    Acta Medica (Hradec Kralove); 2000 Jan 01; 43(1):3-8. PubMed ID: 10934778
    [Abstract] [Full Text] [Related]

  • 31. New insights into molecular pathogenesis of bone marrow failure in paroxysmal nocturnal hemoglobinuria.
    Kawaguchi T, Nakakuma H.
    Int J Hematol; 2007 Jul 01; 86(1):27-32. PubMed ID: 17675263
    [Abstract] [Full Text] [Related]

  • 32. High incidence of transiently appearing complement-sensitive bone marrow precursor cells in patients with severe aplastic anemia--A possible role of high endogenous IL-2 in their suppression.
    Nissen C, Tichelli A, Gratwohl A, Warthmann C, Moser Y, dalle Carbonare V, Sendelov S, Chklovskaia E, Jansen W, Wodnar-Filipowicz A, Sadallah S, Speck B.
    Acta Haematol; 1999 Jul 01; 101(4):165-72. PubMed ID: 10436296
    [Abstract] [Full Text] [Related]

  • 33. Paroxysmal nocturnal hemoglobinuria clones in severe aplastic anemia patients treated with horse anti-thymocyte globulin plus cyclosporine.
    Scheinberg P, Marte M, Nunez O, Young NS.
    Haematologica; 2010 Jul 01; 95(7):1075-80. PubMed ID: 20595102
    [Abstract] [Full Text] [Related]

  • 34. Development of the glycosylphosphatitylinositol-anchoring defect characteristic for paroxysmal nocturnal hemoglobinuria in patients with aplastic anemia.
    Schubert J, Vogt HG, Zielinska-Skowronek M, Freund M, Kaltwasser JP, Hoelzer D, Schmidt RE.
    Blood; 1994 Apr 15; 83(8):2323-8. PubMed ID: 8161800
    [Abstract] [Full Text] [Related]

  • 35. Aplastic anaemia and paroxysmal nocturnal haemoglobinuria: a study of the GPI-anchored proteins on human platelets.
    Vu T, Griscelli-Bennaceur A, Gluckman E, Sigaux F, Carosella ED, Menier C, Scrobohaci ML, Socié G.
    Br J Haematol; 1996 Jun 15; 93(3):586-9. PubMed ID: 8652377
    [Abstract] [Full Text] [Related]

  • 36. Immunophenotypic discrepancies between granulocytic and erythroid lineages in peripheral blood of patients with paroxysmal nocturnal haemoglobinuria.
    Pakdeesuwan K, Wanachiwanawin W, Siripanyaphinyo U, Pattanapanyasat K, Wilairat P, Issaragrisil S.
    Eur J Haematol; 2000 Jul 15; 65(1):8-16. PubMed ID: 10914934
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  • 40. Improved detection and characterization of paroxysmal nocturnal hemoglobinuria using fluorescent aerolysin.
    Brodsky RA, Mukhina GL, Li S, Nelson KL, Chiurazzi PL, Buckley JT, Borowitz MJ.
    Am J Clin Pathol; 2000 Sep 15; 114(3):459-66. PubMed ID: 10989647
    [Abstract] [Full Text] [Related]


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