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Volumn 167, Issue 3, 2013, Pages 1048-1050

Cardiomyopathies and congenital heart diseases in Shwachman-Diamond syndrome: A national survey

Author keywords

Cardiomyopathy; Congenital heart diseases; Shwachman Diamond syndrome

Indexed keywords

ELONGATION FACTOR 1;

EID: 84880918034     PISSN: 01675273     EISSN: 18741754     Source Type: Journal    
DOI: 10.1016/j.ijcard.2012.10.084     Document Type: Article
Times cited : (12)

References (10)
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  • 2
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    • Frequent myocardial lesions in Shwachman's syndrome. Eight fatal cases among 16 Finnish patients
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    • Savilahti, E.1    Rapola, J.2
  • 5
    • 50249135294 scopus 로고    scopus 로고
    • Myocardial function in patients with Shwachman-Diamond syndrome: Aspects to consider before stem cell transplantation
    • S. Toiviainen-Salo, O. Pitkanen, and M. Holmstrom Myocardial function in patients with Shwachman-Diamond syndrome: aspects to consider before stem cell transplantation Pediatr Blood Cancer 51 2008 461 467
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    • P.H. Tsai, I. Sahdev, A. Herry, and J.M. Lipton Fatal cyclophosphamide-induced congestive heart failure in a 10-year-old boy with Shwachman-Diamond syndrome and severe bone marrow failure treated with allogeneic bone marrow transplantation Am J Pediatr Hematol Oncol 12 1990 472 476
    • (1990) Am J Pediatr Hematol Oncol , vol.12 , pp. 472-476
    • Tsai, P.H.1    Sahdev, I.2    Herry, A.3    Lipton, J.M.4
  • 7
    • 84865838762 scopus 로고    scopus 로고
    • Classification of and risk factors for hematologic complications in a French national cohort of 102 patients with Shwachman-Diamond syndrome
    • J. Donadieu, O. Fenneteau, and B. Beaupain Classification of and risk factors for hematologic complications in a French national cohort of 102 patients with Shwachman-Diamond syndrome Haematologica 97 2012 1312 1319
    • (2012) Haematologica , vol.97 , pp. 1312-1319
    • Donadieu, J.1    Fenneteau, O.2    Beaupain, B.3
  • 8
    • 84858335877 scopus 로고    scopus 로고
    • Extended spectrum of human glucose-6-phosphatase catalytic subunit 3 deficiency: Novel genotypes and phenotypic variability in severe congenital neutropenia
    • K. Boztug, P.S. Rosenberg, and M. Dorda Extended spectrum of human glucose-6-phosphatase catalytic subunit 3 deficiency: novel genotypes and phenotypic variability in severe congenital neutropenia J Pediatr 160 2012 679 683
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    • R. Badolato, L. Dotta, and L. Tassone Tetralogy of Fallot is an uncommon manifestation of warts, hypogammaglobulinemia, infections, and myelokathexis syndrome J Pediatr 161 2012 763 765
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    • Cardiac and clinical phenotype in Barth syndrome
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.