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Volumn 312, Issue 4, 1996, Pages 182-186

Lysosomal glycogen storage disease with normal acid maltase: An unusual form of hypertrophic cardiomyopathy with rapidly progressive heart failure

Author keywords

Hypertrophic cardiomyopathy; Lysosomal glycogen storage disease

Indexed keywords

ADOLESCENT; ARTICLE; CASE REPORT; GLYCOGEN METABOLISM; GLYCOGEN STORAGE DISEASE; HEART DILATATION; HEART FAILURE; HEART TRANSPLANTATION; HEART VENTRICLE ARRHYTHMIA; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; MALE; MENTAL DEFICIENCY; SUDDEN DEATH; BLOOD; CONGESTIVE HEART FAILURE; ENZYMOLOGY; LYSOSOME STORAGE DISEASE; METABOLISM; PATHOLOGY; SYNDROME;

EID: 0029817411     PISSN: 00029629     EISSN: None     Source Type: Journal    
DOI: 10.1097/00000441-199610000-00006     Document Type: Article
Times cited : (6)

References (11)
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    • Labrune, P.1    Huguet, P.2    Odievre, M.3
  • 5
    • 0022610542 scopus 로고
    • Dominantly inherited cardioskeletal myopathy with lysosomal glycogen storage and normal acid maltase levels
    • Byme E, Dennett X, Crotty B, Trounce I, Sands M, Hawkins R, et al. Dominantly inherited cardioskeletal myopathy with lysosomal glycogen storage and normal acid maltase levels. Brain. 1986;109:523-36.
    • (1986) Brain , vol.109 , pp. 523-536
    • Byme, E.1    Dennett, X.2    Crotty, B.3    Trounce, I.4    Sands, M.5    Hawkins, R.6
  • 6
    • 0022978582 scopus 로고
    • Familial lethal cardiomyopathy with mental retardation and scapuloperoneal muscular dystrophy
    • Bergia B, Sybers HD, Butler IJ. Familial lethal cardiomyopathy with mental retardation and scapuloperoneal muscular dystrophy. J Neurol Neurosurg Psychiatry. 1986;49:1423-26.
    • (1986) J Neurol Neurosurg Psychiatry , vol.49 , pp. 1423-1426
    • Bergia, B.1    Sybers, H.D.2    Butler, I.J.3
  • 7
  • 8
    • 0025737574 scopus 로고
    • Cardiomyopathy, mental retardation, and autophagic vacuolar myopathy. Abnormal MRI findings in the head
    • Kashio N, Usuki F, Akamine T, Nakagawa S, Higuchi I, Nakahara K, et al. Cardiomyopathy, mental retardation, and autophagic vacuolar myopathy. Abnormal MRI findings in the head. J Neurol Sci. 1991;105:1-5.
    • (1991) J Neurol Sci. , vol.105 , pp. 1-5
    • Kashio, N.1    Usuki, F.2    Akamine, T.3    Nakagawa, S.4    Higuchi, I.5    Nakahara, K.6
  • 9
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    • Lysosomal glycogen storage disease with normal acid maltase: A familial study with successful heart transplant
    • Dworzak F, Casazza F, Mora M, Maria D, Gronda E, Baroldi G, et al. Lysosomal glycogen storage disease with normal acid maltase: A familial study with successful heart transplant. Neuromuscul Disord. 1994;4:243-47.
    • (1994) Neuromuscul Disord. , vol.4 , pp. 243-247
    • Dworzak, F.1    Casazza, F.2    Mora, M.3    Maria, D.4    Gronda, E.5    Baroldi, G.6
  • 10
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    • Glycogen storage disease with normal acid maltase: Skeletal and cardiac muscles
    • Tachi N, Tachi M, Sasaki K, Tomita H, Wakai S, Annaka S, et al. Glycogen storage disease with normal acid maltase: Skeletal and cardiac muscles. Pediatr Neurol. 1989;5:60-65.
    • (1989) Pediatr Neurol. , vol.5 , pp. 60-65
    • Tachi, N.1    Tachi, M.2    Sasaki, K.3    Tomita, H.4    Wakai, S.5    Annaka, S.6
  • 11
    • 0001448360 scopus 로고
    • Glycogen storage disease Type II: Acid α-Glucosidease (Acid Maltase) deficiency
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    • Hirschorn R. Glycogen storage disease Type II: Acid α-Glucosidease (Acid Maltase) deficiency. In: Scriver CR, Beaudet AL, Sly WS, Valle D; eds. The Metabolic Basis of Inherited Disease. 7th ed. (Vol II). New York: McGraw-Hill; 1994;2457-58.
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    • Hirschorn, R.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.