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Vol. 53. Núm. 6.
Páginas 599-600 (diciembre 2000)
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Vol. 53. Núm. 6.
Páginas 599-600 (diciembre 2000)
DOI: 10.1016/S1695-4033(00)77506-0
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M. Bravo Mata*, A. Pérez Muñuzuri, F. Martinón Torres, S. Fernández Cebrián, M. Castro Gago
Departamento de Pediatría. Servicio de Preescolares. Hospital Clínico Universitario. Santiago de Compostela.
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Bibliografía
[1.]
R. Henning, M. South.
Respiratory muscle failure.
pp. 406-409
[2.]
D.C. De Vivo, S. DiMauro.
Hereditary and Acquired types of myopathy. (En) Oski’s Pediatrics: Principles and Practice. CD De Angelis, RD Feigin, JA Mc Millan and JB Warshaw (Eds) 3.ª ed. Lippincott Williams-Wilkins.
Philadelphia, 410 (1999), pp. 1971-1987
[3.]
H.G. Hers.
Alpha glucosidase deficiency in generalized glycogen sotorage diseases (Pompe’s disease).
Biochem J, 86 (1963), pp. 11-16
Medline
[4.]
A. Coppola, A. Munoz, J. Sher.
Morphologic changes of lymphocytes in Pompe disease.
J Pediatr, 93 (5) (1978), pp. 824-826
http://dx.doi.org/10.1016/j.jpeds.2013.04.053 | Medline
[5.]
R. Hirschhorn.
Glycogen storage disease type II: acid alpha glucosidase (acid maltase) deficiency.
1.a, pp. 2443-2464
Copyright © 2002. Asociación Española de Pediatría
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