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Volumn 18, Issue 2, 1997, Pages 143-145

Heart transplantation for Barth syndrome

Author keywords

Barth syndrome; Heart transplantation

Indexed keywords

ALLOGRAFT; ARTICLE; CASE REPORT; CAUSE OF DEATH; DISEASE ASSOCIATION; DISEASE CLASSIFICATION; HEART DILATATION; HEART FAILURE; HEART TRANSPLANTATION; HUMAN; IMMUNE DEFICIENCY; INFANT; MALE; MUSCLE HYPOTONIA; NEUTROPENIA; RECESSIVE INHERITANCE; SEPTICEMIA; SYNDROME;

EID: 0031043089     PISSN: 01720643     EISSN: None     Source Type: Journal    
DOI: 10.1007/s002469900135     Document Type: Article
Times cited : (26)

References (9)
  • 1
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    • Barth syndrome: Clinical features and confirmation of gene localisation to distal Xq 28
    • Ades LC, Gedeon AK, Wilson MJ, et al (1993) Barth syndrome: clinical features and confirmation of gene localisation to distal Xq 28. Am J Med Genet 45:327-334
    • (1993) Am J Med Genet , vol.45 , pp. 327-334
    • Ades, L.C.1    Gedeon, A.K.2    Wilson, M.J.3
  • 2
    • 0020974404 scopus 로고
    • An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes
    • Barth PG, Scholte HR, Berden JA, et al (1983) An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes. J Neurol Sci 62:327-355
    • (1983) J Neurol Sci , vol.62 , pp. 327-355
    • Barth, P.G.1    Scholte, H.R.2    Berden, J.A.3
  • 3
    • 0026344373 scopus 로고
    • Pediatric heart transplantation at Stanford: Results of a 15 year experience
    • Baum D, Bernstein D, Starnes VA, et al (1991) Pediatric heart transplantation at Stanford: results of a 15 year experience. Pediatrics 88:203-214
    • (1991) Pediatrics , vol.88 , pp. 203-214
    • Baum, D.1    Bernstein, D.2    Starnes, V.A.3
  • 4
    • 0026019727 scopus 로고
    • Mapping of a locus for X-linked cardioskeletal myopathy with neutropenia and abnormal mitochondria (Barth syndrome)
    • Bolhuis PA, Hensels GW, Hulsebos TJM, Baas F, Barth PG (1991) Mapping of a locus for X-linked cardioskeletal myopathy with neutropenia and abnormal mitochondria (Barth syndrome). Am J Hum Genet 48:481-485
    • (1991) Am J Hum Genet , vol.48 , pp. 481-485
    • Bolhuis, P.A.1    Hensels, G.W.2    Hulsebos, T.J.M.3    Baas, F.4    Barth, P.G.5
  • 5
    • 0027185370 scopus 로고
    • Multiple respiratory chain abnormalities associated with hypertrophic cardiomyopathy and 3-methylglutaconic aciduria
    • Ibel H, Endres W, Hadorn HB, et al (1993) Multiple respiratory chain abnormalities associated with hypertrophic cardiomyopathy and 3-methylglutaconic aciduria. Eur J Pediatr 152:665-670
    • (1993) Eur J Pediatr , vol.152 , pp. 665-670
    • Ibel, H.1    Endres, W.2    Hadorn, H.B.3
  • 6
    • 0023683742 scopus 로고
    • Dilated cardiomyopathy with neutropenia, short stature, and abnormal carnitine metabolism
    • Ino T, Sherwood WG, Cutz E, et al (1988) Dilated cardiomyopathy with neutropenia, short stature, and abnormal carnitine metabolism. J Pediatr 113:511-514
    • (1988) J Pediatr , vol.113 , pp. 511-514
    • Ino, T.1    Sherwood, W.G.2    Cutz, E.3
  • 7
    • 0025951140 scopus 로고
    • X-linked dilated cardiomyopathy with neutropenia, growth retardation, and 3-methylglutoconic aciduria
    • Kelley RI, Cheatham JP, Clark BJ, et al (1991) X-linked dilated cardiomyopathy with neutropenia, growth retardation, and 3-methylglutoconic aciduria. J Pediatr 119:738-747
    • (1991) J Pediatr , vol.119 , pp. 738-747
    • Kelley, R.I.1    Cheatham, J.P.2    Clark, B.J.3
  • 8
    • 0018393867 scopus 로고
    • An X-linked recessive cardiomyopathy with abnormal mitochondria
    • Neustein HB, Lurie PR, Dahms B, Takahashi M (1979) An X-linked recessive cardiomyopathy with abnormal mitochondria. Pediatrics 64:24-29
    • (1979) Pediatrics , vol.64 , pp. 24-29
    • Neustein, H.B.1    Lurie, P.R.2    Dahms, B.3    Takahashi, M.4
  • 9
    • 0027742043 scopus 로고
    • Cardiac transplantation in an incomplete Kearns-Sayre syndrome with mitochondrial DNA deletion
    • Tranchant C, Mousson B, Mohr M, et al (1993) Cardiac transplantation in an incomplete Kearns-Sayre syndrome with mitochondrial DNA deletion. Neuromuscul Disord 3:561-566
    • (1993) Neuromuscul Disord , vol.3 , pp. 561-566
    • Tranchant, C.1    Mousson, B.2    Mohr, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.