Clinical and Histologic Ocular Findings in Pompe Disease
Author:
Publisher
SLACK, Inc.
Subject
Ophthalmology,General Medicine,Pediatrics, Perinatology and Child Health
Reference34 articles.
1. Acid alpha-glucosidase deficiency (glycogenosis type II, Pompe disease);Raben N;Curr Mol Med.,2002
2. Pompe disease in infants and children;Kishnani PS;J Pediatr.,2004
3. Glycogen storage disease types I and II: treatment updates;Koeberl DD;J Inherit Metab Dis.,2007
4. Over idiopatische hypertrophie van het hart;Pompe JC;Ned Tijdshr Geneeskd.,1932
5. alpha-Glucosidase deficiency in generalized glycogenstorage disease (Pompe's disease);Hers HG;Biochem J.,1963
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4. Minimum Effective Dose to Achieve Biochemical Correction with Adeno-Associated Virus Vector-Mediated Gene Therapy in Mice with Pompe Disease;Human Gene Therapy;2022-05-01
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