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Volumn 41, Issue 2, 2001, Pages 256-263

Mathematical modeling and computer simulation of erythrocytapheresis for SCD

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CASE REPORT; COMPUTER SIMULATION; CYTAPHERESIS; FEMALE; HUMAN; IRON OVERLOAD; MALE; MATHEMATICAL MODEL; SCHOOL CHILD; SICKLE CELL ANEMIA; STROKE;

EID: 0035099784     PISSN: 00411132     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1537-2995.2001.41020256.x     Document Type: Article
Times cited : (6)

References (27)
  • 1
    • 0019805795 scopus 로고
    • The intracellular polymerization of sickle hemoglobin and its relevance to sickle cell disease
    • (1981) Blood , vol.58 , pp. 1057-1068
    • Noguchi, C.T.1    Schechter, A.N.2
  • 8
    • 0023623533 scopus 로고
    • Iron overload and iron chelation therapy in thalassaemia and sickle cell haemoglobinopathies
    • (1987) Acta Haematol , vol.78 , pp. 206-211
    • Pippard, M.J.1
  • 17
    • 0015068811 scopus 로고
    • Comparative studies of height and weight as a blood volume reference standard in normal children and children with sickle cell disease
    • (1971) Am J Clin Pathol , vol.55 , pp. 662-670
    • Gross, S.1    Godel, J.C.2
  • 26
    • 0027958085 scopus 로고
    • Erythrocytapheresis therapy to reduce iron overload in chronically transfused patients with sickle cell disease
    • (1994) Blood , vol.83 , pp. 1136-1142
    • Kim, H.C.1    Dugan, N.P.2    Silber, J.H.3
  • 27
    • 0032735280 scopus 로고    scopus 로고
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.