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Volumn 850, Issue , 1998, Pages 459-460

Increase in hemoglobin concentration during therapy with hydroxyurea in Cooley's anemia

Author keywords

[No Author keywords available]

Indexed keywords

HEMOGLOBIN; HEMOGLOBIN F; HYDROXYUREA;

EID: 0031821279     PISSN: 00778923     EISSN: None     Source Type: Book Series    
DOI: 10.1111/j.1749-6632.1998.tb10520.x     Document Type: Conference Paper
Times cited : (10)

References (9)
  • 1
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    • Hydroxyurea and sickle cell anemia
    • CHARACHE, S. F., B. BARTON, R. D. MOORE, et al. 1996. Hydroxyurea and sickle cell anemia. Medicine 75(6): 300-326.
    • (1996) Medicine , vol.75 , Issue.6 , pp. 300-326
    • Charache, S.F.1    Barton, B.2    Moore, R.D.3
  • 2
    • 0030039970 scopus 로고    scopus 로고
    • Reactivation of fetal hemoglobin in patients with thalassemia
    • OLIVIERI, N. F. 1996. Reactivation of fetal hemoglobin in patients with thalassemia. Sem. Hematol. 33: 24-42.
    • (1996) Sem. Hematol. , vol.33 , pp. 24-42
    • Olivieri, N.F.1
  • 3
    • 0030026994 scopus 로고    scopus 로고
    • Hypertransfusion for spinal cord compression secondary to extramedullary hematopoiesis
    • ANSELM, C. W., K. S. TAI, V. WONG, et al. 1996. Hypertransfusion for spinal cord compression secondary to extramedullary hematopoiesis. Ped. Hematol./Oncol. 13: 89-94.
    • (1996) Ped. Hematol./Oncol. , vol.13 , pp. 89-94
    • Anselm, C.W.1    Tai, K.S.2    Wong, V.3
  • 4
    • 0027772636 scopus 로고
    • Cauda equina compression syndrome in a patient affected by thalassemia intermedia: Complete regression with blood transfusion therapy
    • MANCUSO, P., A. ZINGALE, L. BASILE, et al. 1993. Cauda equina compression syndrome in a patient affected by thalassemia intermedia: Complete regression with blood transfusion therapy. Child's Nerv. Syst. 9: 440-441.
    • (1993) Child's Nerv. Syst. , vol.9 , pp. 440-441
    • Mancuso, P.1    Zingale, A.2    Basile, L.3
  • 5
    • 0027409287 scopus 로고
    • Molecular characterization of beta-thalassemia in Egyptians
    • HUSSEIN, I. R., S. A. TEMTAMY, A. EL-BESHLAWY, et al. 1993. Molecular characterization of beta-thalassemia in Egyptians. Human Mutation 2(1): 48-52.
    • (1993) Human Mutation , vol.2 , Issue.1 , pp. 48-52
    • Hussein, I.R.1    Temtamy, S.A.2    El-Beshlawy, A.3
  • 6
    • 0023782895 scopus 로고
    • Clinical and genetic heterogeneity in black patients with homozygous β-thalassemia from the southeastern United States
    • GONZALEZ-REDONDO J. M., T. A. STOMING, K. D. LANCLOS, et al. 1988. Clinical and genetic heterogeneity in black patients with homozygous β-thalassemia from the southeastern United States. Blood 72(3): 1007-1014.
    • (1988) Blood , vol.72 , Issue.3 , pp. 1007-1014
    • Gonzalez-Redondo, J.M.1    Stoming, T.A.2    Lanclos, K.D.3
  • 7
    • 0024592813 scopus 로고
    • β-thalassemia due to two novel nucleotide substitutions in consensus acceptor splice sequences of the β-globin gene
    • WONG, C., S. E. ANTONARAKIS, S. C. GOFF, et al. 1989. β-thalassemia due to two novel nucleotide substitutions in consensus acceptor splice sequences of the β-globin gene. Blood 73: 914-918.
    • (1989) Blood , vol.73 , pp. 914-918
    • Wong, C.1    Antonarakis, S.E.2    Goff, S.C.3
  • 8
    • 0025805101 scopus 로고
    • β-thalassemia, Hb S-β-thalassemia and sickle cell anemia among Tunisians
    • FATTOUM, S., F. GUERMIRA, C. ONER, et al. 1991. β-thalassemia, Hb S-β-thalassemia and sickle cell anemia among Tunisians. Hemoglobin 15: 11-21.
    • (1991) Hemoglobin , vol.15 , pp. 11-21
    • Fattoum, S.1    Guermira, F.2    Oner, C.3
  • 9
    • 18744428231 scopus 로고
    • Molecular basis of beta-thalassaemia in Japan: Heterogeneity and origins of mutations
    • WAKAMATSU, C., M. ICHINOSE, J. MANABE, et al. 1994. Molecular basis of beta-thalassaemia in Japan: Heterogeneity and origins of mutations. Acta Haematologica 91(3): 136-143.
    • (1994) Acta Haematologica , vol.91 , Issue.3 , pp. 136-143
    • Wakamatsu, C.1    Ichinose, M.2    Manabe, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.