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William W Motley

Showing results (1-10 of 21) with videos related to

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Trends in Neurosciences|February 16, 2010
GARS axonopathy: not every neuron's cup of tRNAWilliam W Motley, Kevin Talbot, Kenneth H Fischbeck
Neurology. Genetics|August 18, 2020
Isoform-specific loss of dystonin causes hereditary motor and sensory neuropathyWilliam W Motley, Stephan Züchner, Steven S Scherer
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|June 20, 2008
Eikenella corrodens as a causative agent for neonatal conjunctivitisManpreet S Chhabra, William W Motley, Joel E Mortensen
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|May 8, 2010
Surgical management of infantile cataracts in dystrophic epidermolysis bullosaWilliam W Motley, Deborah K Vanderveen, Constance E West
SAGE Open Medicine|July 7, 2017
Surgical, medical and developmental outcomes in patients with Down syndrome and cataractsStephanie L Santoro, Dema Atoum, Robert B Hufnagel, et al.
Human Molecular Genetics|June 23, 2011
Increasing expression and decreasing degradation of SMN ameliorate the spinal muscular atrophy phenotype in miceDeborah Y Kwon, William W Motley, Kenneth H Fischbeck, et al.
Journal of the Peripheral Nervous System : JPNS|January 18, 2018
A mutation in the heptad repeat 2 domain of MFN2 in a large CMT2A familyLois Dankwa, Jessica Richardson, William W Motley, et al.
Retina (Philadelphia, Pa.)|February 4, 2005
Pseudomonas aeruginosa endogenous endophthalmitis with choroidal abscess in a patient with cystic fibrosisWilliam W Motley, James J Augsburger, Robert K Hutchins, et al.
Neuromuscular Disorders : NMD|January 16, 2019
A novel MFN2 mutation causes variable clinical severity in a multi-generational CMT2 familyLois Dankwa, Jessica Richardson, William W Motley, et al.
Human Molecular Genetics|May 15, 2015
Dominant, toxic gain-of-function mutations in gars lead to non-cell autonomous neuropathologyStuart J Grice, James N Sleigh, William W Motley, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Trends in Neurosciences|February 16, 2010
GARS axonopathy: not every neuron's cup of tRNAWilliam W Motley, Kevin Talbot, Kenneth H Fischbeck
Neurology. Genetics|August 18, 2020
Isoform-specific loss of dystonin causes hereditary motor and sensory neuropathyWilliam W Motley, Stephan Züchner, Steven S Scherer
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|June 20, 2008
Eikenella corrodens as a causative agent for neonatal conjunctivitisManpreet S Chhabra, William W Motley, Joel E Mortensen
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|May 8, 2010
Surgical management of infantile cataracts in dystrophic epidermolysis bullosaWilliam W Motley, Deborah K Vanderveen, Constance E West
SAGE Open Medicine|July 7, 2017
Surgical, medical and developmental outcomes in patients with Down syndrome and cataractsStephanie L Santoro, Dema Atoum, Robert B Hufnagel, et al.
Human Molecular Genetics|June 23, 2011
Increasing expression and decreasing degradation of SMN ameliorate the spinal muscular atrophy phenotype in miceDeborah Y Kwon, William W Motley, Kenneth H Fischbeck, et al.
Journal of the Peripheral Nervous System : JPNS|January 18, 2018
A mutation in the heptad repeat 2 domain of MFN2 in a large CMT2A familyLois Dankwa, Jessica Richardson, William W Motley, et al.
Retina (Philadelphia, Pa.)|February 4, 2005
Pseudomonas aeruginosa endogenous endophthalmitis with choroidal abscess in a patient with cystic fibrosisWilliam W Motley, James J Augsburger, Robert K Hutchins, et al.
Neuromuscular Disorders : NMD|January 16, 2019
A novel MFN2 mutation causes variable clinical severity in a multi-generational CMT2 familyLois Dankwa, Jessica Richardson, William W Motley, et al.
Human Molecular Genetics|May 15, 2015
Dominant, toxic gain-of-function mutations in gars lead to non-cell autonomous neuropathologyStuart J Grice, James N Sleigh, William W Motley, et al.
Pageof 3