Falk, Darin J.
4 papers on CoChatORCID 0000-0002-0645-7867
Most cited papers
- Verified
Pompe disease gene therapy
Byrne, B. J., Falk, D. J., Pacak, C. A., Nayak, S., Herzog, R. W., Elder, M. E., Collins, S. W., Conlon, T. J., Clement, N., Cleaver, B. D., et al. (2011) · Human Molecular Genetics
Lysosomal Storage Disorders ResearchGlycogen Storage Diseases and Myoclonus
Cited by 91
- Verified
Pompe disease gene therapy: neural manifestations require consideration of CNS directed therapy
Byrne, B. J., Fuller, D. D., Smith, B. K., Clement, N., Coleman, K., Cleaver, B., Vaught, L., Falk, D. J., McCall, A., & Corti, M. (2019) · Annals of Translational Medicine
Lysosomal Storage Disorders ResearchGlycogen Storage Diseases and Myoclonus
Cited by 51
- Verified · note
Correcting Neuromuscular Deficits With Gene Therapy in Pompe Disease
Todd, A. G., McElroy, J. A., Grange, R. W., Fuller, D. D., Walter, G. A., Byrne, B. J., & Falk, D. J. (2015) · Annals of Neurology
Lysosomal Storage Disorders ResearchGlycogen Storage Diseases and Myoclonus
Cited by 51
- Verified
Altered activation of the tibialis anterior in individuals with Pompe disease: Implications for motor unit dysfunction: Neuromuscular Activation in Pompe
Corti, M., Smith, B. K., Falk, D. J., Lawson, L. A., Fuller, D. D., Subramony, S. H., Byrne, B. J., & Christou, E. A. (2015) · Muscle & Nerve
Lysosomal Storage Disorders ResearchMuscle Physiology and Disorders
Cited by 20
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