L-alanine supplementation in late infantile glycogen storage disease type II

Pediatric Neurology

Volumn 27, Issue 2, 2002, Pages 145-146

  Bodamer, Olaf A ^a,d   Haas, Dorothea ^b   Hermans, Monique M ^c   Reuser, Arnold J ^c   Hoffmann, Georg F ^b  

^a University Children's Hospital Vienna   (Germany)

^b UNIVERSITY HOSPITAL HEIDELBERG   (Germany)

^c ERASMUS UNIVERSITY ROTTERDAM   (Netherlands)

^d UNIVERSITY OF VIENNA   (Austria)

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE; GLYCOGEN;

ARTICLE; CARDIOMYOPATHY; CASE REPORT; CLINICAL FEATURE; CLINICAL TRIAL; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; DEVELOPMENTAL DISORDER; DISEASE COURSE; GLYCOGEN STORAGE DISEASE TYPE 2; HUMAN; INFANT; MALE; MUSCLE HYPOTONIA; ONSET AGE; PRIORITY JOURNAL; SUPPLEMENTATION; TIME;

EID: 0036696996     PISSN: 08878994     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0887-8994(02)00413-7     Document Type: Article

References (9)

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2. Bijvoet A.G., Van Hirtum H., Kroos M.A., et al. Human acid alpha-glucosidase from rabbit milk has therapeutic effect in mice with glycogen storage disease type II. Hum Mol Genet. 8:1999;2145-2153
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6. Slonim A.E., Coleman R.A., McElligot M.A., et al. Improvement of muscle function in acid maltase deficiency by high-protein therapy. Neurology. 33:1983;34-38
7. Bodamer O.A.F., Halliday D., Leonard J.V. The effects of L-alanine supplementation in late-onset glycogen storage disease type II. Neurology. 55:2000;710-712
8. Slonim A.E., Bulone L., Ritz S., Goldberg T., Chen A., Martiniuk F. Identification of two subtypes of infantile acid maltase deficiency. J Pediatr. 137:2000;283-285
9. Reuser A.J.J., Koster J.F., Hoogeveen A., Galjaard H. Biochemical, immunological and cell genetic studies in glycogenosis type II. Am J Hum Genet. 30:1978;132-143