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Volumn 72, Issue 2, 2000, Pages 206-209

Two cases showing clonal progression with full evolution from aplastic anemia-paroxysmal nocturnal hemoglobinuria syndrome to myelodysplastic syndromes and leukemia

Author keywords

Aplastic anemia; Leukemia; Myelodysplastic syndromes; PNH; Wilms' tumor gene

Indexed keywords

ADULT; AGED; APLASTIC ANEMIA; ARTICLE; CASE REPORT; CELL CLONE; CELL LINEAGE; CHROMOSOME ANALYSIS; DISEASE COURSE; FEMALE; FLOW CYTOMETRY; GENETICS; HUMAN; LEUKEMIA; MALE; MYELODYSPLASTIC SYNDROME; PAROXYSMAL NOCTURNAL HEMOGLOBINURIA; PATHOLOGY; TUMOR SUPPRESSOR GENE;

EID: 0034243671     PISSN: 09255710     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (14)

References (3)
  • 1
    • 0030912049 scopus 로고    scopus 로고
    • The pathophysiology of acquired aplastic anemia
    • Young NS, Maciejewski J.The pathophysiology of acquired aplastic anemia. N Engl J Med. 1997;336:1365-1372.
    • (1997) N Engl J Med. , vol.336 , pp. 1365-1372
    • Young, N.S.1    Maciejewski, J.2
  • 3
    • 0028338781 scopus 로고
    • Paroxysmal nocturnal hemoglobinuria and the glycosylphosphatidylinositol anchor
    • Yeh ETH, Rosse WF. Paroxysmal nocturnal hemoglobinuria and the glycosylphosphatidylinositol anchor. J Clin Invest. 1994;93:2305-2310.
    • (1994) J Clin Invest. , vol.93 , pp. 2305-2310
    • Yeh, E.T.H.1    Rosse, W.F.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.