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Volumn 38, Issue 4, 2001, Pages 315-323

Principles and problems of transfusion in sickle cell disease

Author keywords

[No Author keywords available]

Indexed keywords

HEMOGLOBIN S;

EID: 0034778419     PISSN: 00371963     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0037-1963(01)90025-3     Document Type: Article
Times cited : (55)

References (86)
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    • Preoperative Transfusion in Sickle Cell Disease Study Group
    • (1997) Blood , vol.89 , pp. 1533-1542
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  • 28
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    • Erythrocytapheresis for chronically transfused children with sickle cell disease: An effective method for maintaining a low hemoglobin S level and reducing iron overload
    • (1999) J Clin Apheresis , vol.14 , pp. 122-125
    • Singer, S.T.1    Quirolo, K.2    Nishi, K.3
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    • abstr
    • (1999) Transfusion , vol.39 , Issue.SUPPL. , pp. 97
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    • (1995) N Engl J Med , vol.333 , pp. 206-213
    • Vichinsky, E.P.1    Neumayr, L.D.2    Haberkern, C.3
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    • Consensus document for transfusion-related iron overload
    • (2001) Semin Hematol , vol.38 , Issue.SUPPL. 1 , pp. 2-4
    • Vichinsky, E.1
  • 83
    • 0026034335 scopus 로고
    • High risk of recurrent stroke after discontinuance of five to twelve years of transfusion therapy in patients with sickle cell disease
    • (1991) J Pediatr , vol.118 , pp. 377-382
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.