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Progress in Molecular Biology and Translational Science|June 27, 2021
Gene editing and modulation for Duchenne muscular dystrophyAnthony A Stephenson, Kevin M Flanigan
Seminars in Neurology|November 3, 2012
The muscular dystrophiesKevin M Flanigan
Neurologic Clinics|July 20, 2014
Duchenne and Becker muscular dystrophiesKevin M Flanigan
Seminars in Pediatric Neurology|April 24, 2021
Update in the MucopolysaccharidosesKim L McBride, Kevin M Flanigan
Current Opinion in Neurology|July 26, 2019
Update in Duchenne and Becker muscular dystrophyMegan A Waldrop, Kevin M Flanigan
Neurology. Genetics|October 21, 2016
Reassessing carrier status for dystrophinopathiesTara M Newcomb, Kevin M Flanigan
Physical Medicine and Rehabilitation Clinics of North America|September 4, 2012
A practical approach to molecular diagnostic testing in neuromuscular diseasesW David Arnold, Kevin M Flanigan
Molecular Therapy. Methods & Clinical Development|September 14, 2023
CRISPR-Cas9 homology-independent targeted integration of exons 1-19 restores full-length dystrophin in miceAnthony A Stephenson, Stefan Nicolau, Tatyana A Vetter, et al.
Pediatric Clinics of North America|May 30, 2015
Genetics and emerging treatments for Duchenne and Becker muscular dystrophyNicolas Wein, Lindsay Alfano, Kevin M Flanigan
Neurology|July 27, 2005
Clinical and electrophysiologic features of CMT2A with mutations in the mitofusin 2 geneVictoria H Lawson, Brad V Graham, Kevin M Flanigan
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