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Volumn 42, Issue 4, 2008, Pages 293-294

Unrelated cord blood transplantation in a girl with Hoyeraal-Hreidarsson syndrome

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOPHOSPHAMIDE; CYCLOSPORIN A; FLUDARABINE; GRANULOCYTE COLONY STIMULATING FACTOR; MYCOPHENOLIC ACID; PREDNISOLONE; THYMOCYTE ANTIBODY;

EID: 51049109411     PISSN: 02683369     EISSN: 14765365     Source Type: Journal    
DOI: 10.1038/bmt.2008.163     Document Type: Article
Times cited : (11)

References (11)
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    • Knight SW, Heiss NS, Vulliamy TJ, Aalfs CM, McMahon C, Richond P et al. Unexplained aplastic anaemia, immuno-deficiency, and cerebellar hypoplasia (Hoyeraal-Hreidarsson syndrome) due to mutations in the dyskeratosis congenita gene. DKC1. J Haematol 1999; 107: 335-339.
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  • 2
    • 0028916022 scopus 로고    scopus 로고
    • Aalfs C, v den Berg H, Barth Hennekam RCM. The Hoyeraal-Hreidarsson syndrome: The fourth case of a separate entity with prenatal growth failure, progressive pancytopenia and cerebellar hypoplasia. Eur J Pediatr 1995; 154: 304-308.
    • Aalfs C, v den Berg H, Barth PG, Hennekam RCM. The Hoyeraal-Hreidarsson syndrome: The fourth case of a separate entity with prenatal growth failure, progressive pancytopenia and cerebellar hypoplasia. Eur J Pediatr 1995; 154: 304-308.
  • 3
    • 0023731072 scopus 로고
    • A syndrome of progressive pancytopenia with microcephaly, cerebellar hypoplasia and growth failure
    • Hreidarsson S, Kristjansson K, Johannesson G, Johannsson JH. A syndrome of progressive pancytopenia with microcephaly, cerebellar hypoplasia and growth failure. Acta Paediatr Scand 1988; 77: 773-775.
    • (1988) Acta Paediatr Scand , vol.77 , pp. 773-775
    • Hreidarsson, S.1    Kristjansson, K.2    Johannesson, G.3    Johannsson, J.H.4
  • 4
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    • Association between aplastic anaemia and mutations in telomerase RNA
    • Vulliamy T, Marrone A, Dokal I, Mason PJ. Association between aplastic anaemia and mutations in telomerase RNA. Lancet 2002; 359: 2168-2170.
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    • Vulliamy, T.1    Marrone, A.2    Dokal, I.3    Mason, P.J.4
  • 6
    • 0042441121 scopus 로고    scopus 로고
    • Rapid and complete donor chimerism in adult recipients of unrelated donor umbilical cord blood transplantation after reduced-intensity conditioning
    • Barker JN, Weisdorf DJ, DeFor TE, Blazar BR, Miller JS, Wagner JE. Rapid and complete donor chimerism in adult recipients of unrelated donor umbilical cord blood transplantation after reduced-intensity conditioning. Blood 2001; 102: 1915-1919.
    • (2001) Blood , vol.102 , pp. 1915-1919
    • Barker, J.N.1    Weisdorf, D.J.2    DeFor, T.E.3    Blazar, B.R.4    Miller, J.S.5    Wagner, J.E.6
  • 7
    • 0036435057 scopus 로고    scopus 로고
    • A novel DKC1 mutation, severe combined immunodeficiency (T + B-NK-SCID) and bone marrow transplantation in an infant with Hoyeraal-Hreidarsson syndrome
    • Cossu F, Vulliamy T, Marrone A, Badiali M, Cao A, Dokal I. A novel DKC1 mutation, severe combined immunodeficiency (T + B-NK-SCID) and bone marrow transplantation in an infant with Hoyeraal-Hreidarsson syndrome. Br J Haematol 2002; 119: 765-768.
    • (2002) Br J Haematol , vol.119 , pp. 765-768
    • Cossu, F.1    Vulliamy, T.2    Marrone, A.3    Badiali, M.4    Cao, A.5    Dokal, I.6
  • 8
    • 0345306274 scopus 로고    scopus 로고
    • Sensitivity to radiation and alkylation agent of peripheral lymphocytes and fibroblasts in a Hoyeraal-Hreidarsson syndrome patient
    • M'kacher R, Laithier V, Valent A, Delhommeau F, Violot D, Deutsch E et al. Sensitivity to radiation and alkylation agent of peripheral lymphocytes and fibroblasts in a Hoyeraal-Hreidarsson syndrome patient. Pediatr Hematol Oncol 2003; 20: 651-656.
    • (2003) Pediatr Hematol Oncol , vol.20 , pp. 651-656
    • M'kacher, R.1    Laithier, V.2    Valent, A.3    Delhommeau, F.4    Violot, D.5    Deutsch, E.6
  • 9
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    • Chakrabarti S, Mackinnon S, Chopra R, Kottaridis PD, Peggs K, O'Gorman P. Incidence of CMV infection after nonmyeloblative stem cell transplantation: Potential role for Campath-1H in delaying immune reconstitution. Blood 2002; 99: 4357-4303.
    • (2002) Blood , vol.99 , pp. 4357-4303
    • Chakrabarti, S.1    Mackinnon, S.2    Chopra, R.3    Kottaridis, P.D.4    Peggs, K.5    O'Gorman, P.6
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    • Familial cerebellar hypoplasia and pancytopenia without chromosomal breakages
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  • 11
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    • A case of Hoyeraal-Hreidarsson syndrome: Delayed myelination and hypoplasia of corpus callosum are other important signs
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.