Blepharoptosis in infantile onset Pompe disease: Histological findings and surgical outcomes
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology
Reference25 articles.
1. Alpha-glucosidase deficiency in generalized glycogenstorage disease (Pompe’s disease);Hers;Biochem. J.,1963
2. Recombinant human acid [alpha]-glucosidase: major clinical benefits in infantile-onset Pompe disease;Kishnani;Neurology.,2007
3. Algorithm for Pompe disease newborn screening: results from the Taiwan screening program;Chiang;Mol. Genet. Metab.,2012
4. Pompe disease in infants: improving the prognosis by newborn screening and early treatment;Chien;Pediatrics.,2009
5. Enzyme replacement therapy for Pompe disease;Angelini;Curr. Neurol. Neurosci. Rep.,2012
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