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Pompe disease gene therapy
Barry J. Byrne
, Darin J. Falk
, Christina A. Pacak
, Sushrusha Nayak
, Roland W. Herzog
, Melissa E. Elder
, Shelley W. Collins
, Thomas J. Conlon
, Nathalie Clement
, Brian D. Cleaver
, Denise A. Cloutier
, Stacy L. Porvasnik
,
Saleem Islam
, Mai K. Elmallah
, Anatole Martin
, Barbara K. Smith
, David D. Fuller
, Lee Ann Lawson
, Cathryn S. Mah
Research output
:
Contribution to journal
›
Article
›
peer-review
81
Citations (Scopus)
Overview
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Medicine and Dentistry
Gene Therapy
100%
Glycogen Storage Disease Type II
100%
Enzyme Replacement Therapy
100%
Diseases
60%
Clinical Trial
40%
Respiratory Failure
20%
Autosomal Recessive Inheritance
20%
Glucan 1,4 Alpha Glucosidase
20%
Hypotonia
20%
Myopathy
20%
Ventricular Hypertrophy
20%
Lysosome Enzyme
20%
Weakness
20%
Cardiopulmonary Insufficiency
20%
Adeno-Associated Virus
20%
Pharmacology, Toxicology and Pharmaceutical Science
Replacement Therapy
100%
Glycogen Storage Disease Type 2
100%
Diseases
60%
Clinical Trial
40%
Preclinical Study
20%
Adeno Associated Virus
20%
Heart Ventricle Hypertrophy
20%
Weakness
20%
Muscle Hypotonia
20%
Myopathy
20%
Cardiopulmonary Insufficiency
20%
Lysosome Enzyme
20%
Glucan 1,4 Alpha Glucosidase
20%
Respiratory Failure
20%
Immunology and Microbiology
Preclinical Study
100%
Autosomal Recessive Inheritance
100%
Adeno Associated Virus
100%
Glucosidase
100%
Neuroscience
Enzyme Replacement Therapy
100%
Hypotonia
20%
Muscle Disorder
20%
Lysosome Enzyme
20%
Glucan 1,4 Alpha Glucosidase
20%
Adeno-Associated Virus
20%