Myopathy and growth failure in debrancher enzyme deficiency: Improvement with high-protein nocturnal enteral therapy

Author:

Slonim Alfred E.,Coleman Rosalind A.,Moses W. Shimon

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference15 articles.

1. Disorders of carbohydrate metabolism in infancy,1976

2. Moses WS, Gadoth N, Bashan N, Ben-David E, Slonim AE, Wanderman KL: Neuromuscular involvement in glycogen storage disease type III. Pediatr Res (In press.)

3. Reversal of debrancher deficiency myopathy by the use of high-protein nutrition;Slonim;Ann Neurol,1982

4. Glycogen storage disease type I, III, IV, V, VII and unclassified glycogenosis;Brown,1968

5. The determination of amylo-1,6-glucosidase;Hers;Eur J Biochem,1967

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