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Volumn 84, Issue 6, 2009, Pages 372-373

Sustained and full fetal hemoglobin production after failure of bone marrow transplant in a patient homozygous for beta 0-thalassemia: A clinical remission despite genetic disease and transplant rejection

Author keywords

[No Author keywords available]

Indexed keywords

HEMOGLOBIN F;

EID: 66849104581     PISSN: 03618609     EISSN: 10968652     Source Type: Journal    
DOI: 10.1002/ajh.21392     Document Type: Article
Times cited : (13)

References (8)
  • 1
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    • The thalassemia syndromes
    • Weatherall DJ, Clegg JB, editors. Oxford, UK: Blackwell Science
    • Weatherall DJ, Clegg JB. The thalassemia syndromes. In: Weatherall DJ, Clegg JB, editors. The Thalassemia Syndromes, 4th ed. Oxford, UK: Blackwell Science; 2001. pp 265-284.
    • (2001) The Thalassemia Syndromes, 4th Ed. , pp. 265-284
    • Weatherall, D.J.1    Clegg, J.B.2
  • 2
    • 0035320886 scopus 로고    scopus 로고
    • Phenotype-genotype relationships in monogenic disease: Lessons from the thalassaemias
    • Weatherall DJ. Phenotype-genotype relationships in monogenic disease: Lessons from the thalassaemias. Nat Rev Genet 2001;2:245-255.
    • (2001) Nat Rev Genet , vol.2 , pp. 245-255
    • Weatherall, D.J.1
  • 3
    • 0037304503 scopus 로고    scopus 로고
    • Stem cell transplantation for hemoglobinopaties
    • Gaziev J, Lucarelli G. Stem cell transplantation for hemoglobinopaties. Curr Opin Pediatr 2003;81:24-31.
    • (2003) Curr Opin Pediatr , vol.81 , pp. 24-31
    • Gaziev, J.1    Lucarelli, G.2
  • 4
    • 0025070260 scopus 로고
    • Bone marrow transplantation in patients with thalassemia
    • Lucarelli G, Galimberti M, Polchi P, et al. Bone marrow transplantation in patients with thalassemia. N Engl J Med 1990;322:417-421.
    • (1990) N Engl J Med , vol.322 , pp. 417-421
    • Lucarelli, G.1    Galimberti, M.2    Polchi, P.3
  • 5
    • 29744438595 scopus 로고    scopus 로고
    • Bone marrow transplant in adults with thalassemia: Treatment and long-term follow-up
    • Gaziev J, Sodani P, Polchi P, et al. Bone marrow transplant in adults with thalassemia: Treatment and long-term follow-up. Ann N Y Acad Sci 2005; 1054:196-205.
    • (2005) Ann N Y Acad Sci , vol.1054 , pp. 196-205
    • Gaziev, J.1    Sodani, P.2    Polchi, P.3
  • 6
    • 0029153477 scopus 로고
    • Transplanted sickle-cell disease patients with autologous bone marrow recovery after graft failure develop increased levels of fetal haemoglobin which corrects disease severity
    • Ferster A, Corazza F, Vertongen F, et al. Transplanted sickle-cell disease patients with autologous bone marrow recovery after graft failure develop increased levels of fetal haemoglobin which corrects disease severity. BJH 1995;90:804-808.
    • (1995) BJH , vol.90 , pp. 804-808
    • Ferster, A.1    Corazza, F.2    Vertongen, F.3
  • 7
    • 30444432407 scopus 로고    scopus 로고
    • Regulation of human fetal haemoglobin: New players, new complexities
    • Bank A. Regulation of human fetal haemoglobin: New players, new complexities. Blood 2006;107:435-443.
    • (2006) Blood , vol.107 , pp. 435-443
    • Bank, A.1
  • 8
    • 11144220892 scopus 로고    scopus 로고
    • A sustained and pancellular reversal of γ-globin gene silencing in adult human erythroid precursor cells
    • Bhanu NV, Trice TA, Lee TY, et al. A sustained and pancellular reversal of γ-globin gene silencing in adult human erythroid precursor cells. Blood 2005;105:387-393.
    • (2005) Blood , vol.105 , pp. 387-393
    • Bhanu, N.V.1    Trice, T.A.2    Lee, T.Y.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.