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Volumn 15, Issue 3, 1998, Pages 271-276

α-thalassemia and hereditary spherocytosis in the same patient: The interaction of two diseases

Author keywords

Alpha thalassemia; Hereditary spherocytosis

Indexed keywords

HEMOGLOBIN H;

EID: 0031841567     PISSN: 08880018     EISSN: None     Source Type: Journal    
DOI: 10.3109/08880019809028796     Document Type: Article
Times cited : (6)

References (9)
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  • 2
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    • The combination of hereditary spherocytosis and heterozygous beta thalassaemia
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  • 3
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    • Occurrence of hereditary spheroeytosis and beta thalassemia in the same family: Globin chain synthesis and viscodiffractometric studies
    • Pautard B, Feo C, Dhermy D, Wajcman H, Chich VB. Occurrence of hereditary spheroeytosis and beta thalassemia in the same family: globin chain synthesis and viscodiffractometric studies. Br J Haematol. 1988;70:239-245.
    • (1988) Br J Haematol , vol.70 , pp. 239-245
    • Pautard, B.1    Feo, C.2    Dhermy, D.3    Wajcman, H.4    Chich, V.B.5
  • 4
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    • Coexistence of hereditary spherocytosis (HS) due to band 3 deficiency and beta thalassemia trait: Partial correction of HS phenotype
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  • 5
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    • Interaction of hereditary spherocytosis and alpha thalassemia: A family study
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    • Li, C.1    Heung, M.2    Cheung, K.3    Lam, T.4
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    • Disorders of the red cell membrane
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    • Becker, P.S.1    Lux, S.E.2
  • 7
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    • Recurrent acute splenic sequestration crisis due to interacting genetic defects: Hemoglobin SC disease and hereditary spherocytosis
    • Warkentin TE, Barr RD, Ali AM, Mohandas N. Recurrent acute splenic sequestration crisis due to interacting genetic defects: hemoglobin SC disease and hereditary spherocytosis. Blood. 1990;75:266-270.
    • (1990) Blood , vol.75 , pp. 266-270
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    • Hematological evaluation of patients with various combination of alpha thalassemia
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  • 9
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    • Hematologic complications of liver disease and alcoholism
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    • Solomon, L.R.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.