Ocular and Histologic Findings in a Series of Children With Infantile Pompe Disease Treated With Enzyme Replacement Therapy-Reference-Cited by-同舟云学术

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Ocular and Histologic Findings in a Series of Children With Infantile Pompe Disease Treated With Enzyme Replacement Therapy

Published:2014-11 Issue:6 Volume:51 Page:355-362
ISSN:0191-3913
Container-title:Journal of Pediatric Ophthalmology & Strabismus
language:en
Short-container-title:J Pediatr Ophthalmol Strabismus

Author:

Prakalapakorn S. Grace,Proia Alan D.,Yanovitch Tammy L.,DeArmey Stephanie,Mendelsohn Nancy J.,Aleck Kyrieckos A.,Kishnani Priya S.

Publisher

SLACK, Inc.

Subject

Ophthalmology,General Medicine,Pediatrics, Perinatology, and Child Health

Reference14 articles.

1. Pompe disease diagnosis and management guideline

2. Identification of two subtypes of infantile acid maltase deficiency

3. A retrospective, multinational, multicenter study on the natural history of infantile-onset Pompe disease

4. Early Treatment With Alglucosidase Alfa Prolongs Long-Term Survival of Infants With Pompe Disease

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1. Clinical insight meets scientific innovation to develop a next generation ERT for Pompe disease;Molecular Genetics and Metabolism;2024-09

2. Manifestations of systemic disease in the retina and fundus of cats and dogs;Frontiers in Veterinary Science;2024-02-20

3. Intravitreal enzyme replacement for inherited retinal diseases;Current Opinion in Ophthalmology;2023-12-26

4. Speech Disorders in Children With Pompe Disease: Articulation, Resonance, and Voice Measures;American Journal of Speech-Language Pathology;2023-07-10

5. Blepharoptosis in infantile onset Pompe disease: Histological findings and surgical outcomes;Molecular Genetics and Metabolism Reports;2023-06

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