Art
J-GLOBAL ID：200902224679348806
Reference number：06A0693873
Clinical Significance of a Small Population of Paroxysmal Nocturnal Hemoglobinuria-Type Cells in the Management of Bone Marrow Failure
骨髄不全の管理における小集団の発作性夜間血色素尿症型細胞の臨床的意義
Author (3)：
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Material：
Volume：
84
Issue：
2
Page：
118-122
Publication year：
Aug. 15, 2006
JST Material Number：
F0888A
ISSN：
0925-5710
CODEN：
IJHEEY
Document type：
Article
Article type：
解説
Country of issue：
Germany, Federal Republic of (DEU)
Language：
ENGLISH (EN)
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JST classification (2)：
JST classification
Category name(code) classified by JST.
Hematologic diseases
, Biochemical analytical methods
Reference (20)：
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TAKEDA, J. Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria. Cell. 1993, 73, 703-711
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GRISCELLI-BENNACEUR, A. Aplastic anemia and paroxysmal nocturnal hemoglobinuria : search for a pathogenetic link. Blood. 1995, 85, 1354-1363
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SCHUBERT, J. Development of the glycosylphosphatitylinositol-anchoring defect characteristic for paroxysmal nocturnal hemoglobinuria in patients with aplastic anemia. Blood. 1994, 83, 2323-2328
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PARKER, C. Diagnosis and management of paroxysmal nocturnal hemoglobinuria. Blood. 2005, 106, 3699-3709
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DUNN, DE. Paroxysmal nocturnal hemoglobinuria cells in patients with bone marrow failure syndromes. Ann Intern Med. 1999, 131, 401-408
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