l-alanine supplementation in late infantile glycogen storage disease type II-Reference-Cited by-同舟云学术

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

Published:2002-08 Issue:2 Volume:27 Page:145-146
ISSN:0887-8994
Container-title:Pediatric Neurology
language:en
Short-container-title:Pediatric Neurology

Author:

Bodamer Olaf A,Haas Dorothea,Hermans Monique M,Reuser Arnold J,Hoffmann Georg F

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,Neurology,Pediatrics, Perinatology, and Child Health

Reference9 articles.

1. Glycogen storage disease type II;Hirschhorn,2001

2. Human acid alpha-glucosidase from rabbit milk has therapeutic effect in mice with glycogen storage disease type II;Bijvoet;Hum Mol Genet,1999

3. Recombinant human α-glucosidase from rabbit milk in Pompe patients;Van den Hout;Lancet,2000

4. Respiratory insufficiency in acid maltase deficiency;Demey;J Parenter Enteral Nutr,1989

5. Acid maltase deficiency;Isaacs;J Neurol Neurosurg Psychiatry,1986

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3. Nutrition in adult patients with selected lysosomal storage diseases;Nutrition, Metabolism and Cardiovascular Diseases;2021-03

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