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Volumn 42, Issue 6, 2010, Pages 455-458

Acute Progression of Neuromuscular Findings in Infantile Pompe Disease

Author keywords

[No Author keywords available]

Indexed keywords

RECOMBINANT GLUCAN 1,4 ALPHA GLUCOSIDASE;

EID: 77952106962     PISSN: 08878994     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.pediatrneurol.2010.02.006     Document Type: Article
Times cited : (43)

References (11)
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    • Scriver C.R., Beaudet A.L., Sly W.S., Valle D., Kinzler K.E., and Vogelstein B. (Eds), McGraw-Hill, New York
    • Hirschhorn R., and Reuser A.J.J. Glycogen storage disease type II: Acid α-glucosidase (acid maltase) deficiency. In: Scriver C.R., Beaudet A.L., Sly W.S., Valle D., Kinzler K.E., and Vogelstein B. (Eds). The metabolic and molecular bases of inherited diseases (2001), McGraw-Hill, New York 3389-3420
    • (2001) The metabolic and molecular bases of inherited diseases , pp. 3389-3420
    • Hirschhorn, R.1    Reuser, A.J.J.2
  • 3
    • 0015093712 scopus 로고
    • Nervous system in Pompe's disease. Ultrastructure and biochemistry
    • Gambetti P., Dimauro S., and Baker L. Nervous system in Pompe's disease. Ultrastructure and biochemistry. J Neuropathol Exp Neurol 30 (1971) 412-430
    • (1971) J Neuropathol Exp Neurol , vol.30 , pp. 412-430
    • Gambetti, P.1    Dimauro, S.2    Baker, L.3
  • 5
    • 0037556563 scopus 로고
    • Pompe's disease (diffuse glycogenosis) with neuronal storage
    • Mancall E.L., Aponte G.E., and Berry R.G. Pompe's disease (diffuse glycogenosis) with neuronal storage. J Neuropathol Exp Neurol 24 (1965) 85-96
    • (1965) J Neuropathol Exp Neurol , vol.24 , pp. 85-96
    • Mancall, E.L.1    Aponte, G.E.2    Berry, R.G.3
  • 6
    • 0015929582 scopus 로고
    • Pompe's disease: An inborn lysosomal disorder with storage of glycogen. A study of brain and striated muscle
    • Martin J.J., de Barsy T., van Hoof F., and Palladini G. Pompe's disease: An inborn lysosomal disorder with storage of glycogen. A study of brain and striated muscle. Acta Neuropathol (Berl) 23 (1973) 229-244
    • (1973) Acta Neuropathol (Berl) , vol.23 , pp. 229-244
    • Martin, J.J.1    de Barsy, T.2    van Hoof, F.3    Palladini, G.4
  • 7
    • 0014774632 scopus 로고
    • Acid maltase deficiency: Comparison of infantile, childhood, and adult types
    • Engel A.G., Seybold M.E., Lambert E.H., and Gomez M.R. Acid maltase deficiency: Comparison of infantile, childhood, and adult types. Neurology 20 (1970) 382
    • (1970) Neurology , vol.20 , pp. 382
    • Engel, A.G.1    Seybold, M.E.2    Lambert, E.H.3    Gomez, M.R.4
  • 9
    • 67249094212 scopus 로고    scopus 로고
    • Neural deficits contribute to respiratory insufficiency in Pompe disease
    • DeRuisseau L.R., Fuller D.D., Qiu K., et al. Neural deficits contribute to respiratory insufficiency in Pompe disease. Proc Natl Acad Sci USA 106 (2009) 9419-9424
    • (2009) Proc Natl Acad Sci USA , vol.106 , pp. 9419-9424
    • DeRuisseau, L.R.1    Fuller, D.D.2    Qiu, K.3
  • 10
    • 0042131675 scopus 로고    scopus 로고
    • The natural course of infantile Pompe's disease: 20 original cases compared with 133 cases from the literature
    • van den Hout H.M., Hop W., van Diggelen O.P., et al. The natural course of infantile Pompe's disease: 20 original cases compared with 133 cases from the literature. Pediatrics 112 (2003) 332-340
    • (2003) Pediatrics , vol.112 , pp. 332-340
    • van den Hout, H.M.1    Hop, W.2    van Diggelen, O.P.3
  • 11
    • 33747609102 scopus 로고    scopus 로고
    • Brain development in infantile-onset Pompe disease treated by enzyme replacement therapy
    • Chien Y.H., Lee N.C., Peng S.F., and Hwu W.L. Brain development in infantile-onset Pompe disease treated by enzyme replacement therapy. Pediatr Res 60 (2006) 349-352
    • (2006) Pediatr Res , vol.60 , pp. 349-352
    • Chien, Y.H.1    Lee, N.C.2    Peng, S.F.3    Hwu, W.L.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.