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Journal Abstract Search

213 related items for PubMed ID: 16467865

  • 1. High frequency of several PIG-A mutations in patients with aplastic anemia and myelodysplastic syndrome.
    Okamoto M, Shichishima T, Noji H, Ikeda K, Nakamura A, Akutsu K, Maruyama Y.
    Leukemia; 2006 Apr; 20(4):627-34. PubMed ID: 16467865
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  • 3. A pathogenetic link between aplastic anemia and paroxysmal nocturnal hemoglobinuria is suggested by a high frequency of aplastic anemia patients with a deficiency of phosphatidylinositol glycan anchored proteins.
    Schrezenmeier H, Hertenstein B, Wagner B, Raghavachar A, Heimpel H.
    Exp Hematol; 1995 Jan; 23(1):81-7. PubMed ID: 7995374
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  • 5. [Clinical and laboratory characteristics in patients of myelodysplastic syndrome with PNH clones].
    Li Y, Qin T, Xu Z, Zhang Y, Wang J, Li B, Fang L, Pan L, Hu N, Zhang H, Qu S, Liu J, Wang H, Xiao Z.
    Zhonghua Xue Ye Xue Za Zhi; 2016 Apr; 37(4):313-7. PubMed ID: 27093995
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  • 6. N-RAS gene mutation in patients with aplastic anemia and aplastic anemia/ paroxysmal nocturnal hemoglobinuria during evolution to clonal disease.
    Mortazavi Y, Tooze JA, Gordon-Smith EC, Rutherford TR.
    Blood; 2000 Jan 15; 95(2):646-50. PubMed ID: 10627475
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  • 7. Paroxysmal nocturnal haemoglobinuria clones in patients with myelodysplastic syndromes.
    Iwanaga M, Furukawa K, Amenomori T, Mori H, Nakamura H, Fuchigami K, Kamihira S, Nakakuma H, Tomonaga M.
    Br J Haematol; 1998 Jul 15; 102(2):465-74. PubMed ID: 9695961
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  • 8. Origin and fate of blood cells deficient in glycosylphosphatidylinositol-anchored protein among patients with bone marrow failure.
    Sugimori C, Mochizuki K, Qi Z, Sugimori N, Ishiyama K, Kondo Y, Yamazaki H, Takami A, Okumura H, Nakao S.
    Br J Haematol; 2009 Oct 15; 147(1):102-12. PubMed ID: 19656154
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  • 9. Genotypic, immunophenotypic and clinical features of Thai patients with paroxysmal nocturnal haemoglobinuria.
    Pramoonjago P, Pakdeesuwan K, Siripanyaphinyo U, Chinprasertsuk S, Kinoshita T, Wanachiwanawin W.
    Br J Haematol; 1999 May 15; 105(2):497-504. PubMed ID: 10233427
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  • 11. Recent insights into the pathophysiology of paroxysmal nocturnal hemoglobinuria.
    Meletis J, Terpos E.
    Med Sci Monit; 2003 Jul 15; 9(7):RA161-72. PubMed ID: 12883466
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  • 12. 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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  • 14. The distribution of PIG-A gene abnormalities in paroxysmal nocturnal hemoglobinuria granulocytes and cultured erythroblasts.
    Noji H, Shichishima T, Saitoh Y, Kai T, Yamamoto T, Ogawa K, Okamoto M, Ikeda K, Maruyama Y.
    Exp Hematol; 2001 Apr 01; 29(4):391-400. PubMed ID: 11301179
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  • 15. Detection of GPI-anchored protein-deficient cells in patients with aplastic anaemia and evidence for clonal expansion during the clinical course.
    Kawaguchi K, Wada H, Mori A, Takemoto Y, Kakishita E, Kanamaru A.
    Br J Haematol; 1999 Apr 01; 105(1):80-4. PubMed ID: 10233366
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  • 16. CD59-deficient blood cells and PIG-A gene abnormalities in Japanese patients with aplastic anaemia.
    Azenishi Y, Ueda E, Machii T, Nishimura J, Hirota T, Shibano M, Nakao S, Kinoshita T, Mizoguchi H, Kitani T.
    Br J Haematol; 1999 Mar 01; 104(3):523-9. PubMed ID: 10086790
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  • 17. [Expression of three kinds of GPI-anchor proteins in paroxysmal nocturnal hemoglobinuria, aplastic anemia and myelodysplastic syndromes patients and their clinical implications].
    Dong XY, Xu CG, Sun GR, Zhang T, Peng J.
    Zhonghua Xue Ye Xue Za Zhi; 2004 Apr 01; 25(4):198-201. PubMed ID: 15182554
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  • 18. Genotypic and phenotypic implications in paroxysmal nocturnal hemoglobinuria (PNH): a preliminary investigation.
    Pakdeesuwan K, Siripanyaphinyo U, Pramoonjago P, Pattanapanyasat K, Wilairat P, Kinoshita T, Wanachiwanawin W.
    Southeast Asian J Trop Med Public Health; 1997 Apr 01; 28 Suppl 3():58-63. PubMed ID: 9640601
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  • 19. 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
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  • 20. Genetic instability and the etiology of somatic PIG-A mutations in paroxysmal nocturnal hemoglobinuria.
    Purow DB, Howard TA, Marcus SJ, Rosse WF, Ware RE.
    Blood Cells Mol Dis; 1999 Apr 01; 25(2):81-91. PubMed ID: 10389589
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