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G Sweeney

Showing results (181-190 of 220) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1995
Bilateral simultaneous optic neuropathy in adults: clinical, imaging, serological, and genetic studiesS P Morrissey, F X Borruat, D H Miller, et al.
Plastic and Reconstructive Surgery|July 27, 2019
Facial Transplantation for an Irreparable Central and Lower Face Injury: A Modernized Approach to a Classic ChallengeRami S Kantar, Daniel J Ceradini, Bruce E Gelb, et al.
Journal of Medical Genetics|March 8, 2011
Kearns-Sayre syndrome caused by defective R1/p53R2 assemblyRobert D S Pitceathly, Elisa Fassone, Jan-Willem Taanman, et al.
Neurobiology of Aging|January 16, 2015
Investigation of next-generation sequencing technologies as a diagnostic tool for amyotrophic lateral sclerosisSarah Morgan, Maryam Shoai, Pietro Fratta, et al.
Brain : a Journal of Neurology|February 26, 2016
In vivo impact of presynaptic calcium channel dysfunction on motor axons in episodic ataxia type 2Susan E Tomlinson, S Veronica Tan, David Burke, et al.
Journal of the Neurological Sciences|January 1, 1994
Mitochondrial DNA mutation underlying Leigh's syndrome: clinical, pathological, biochemical, and genetic studies of a patient presenting with progressive myoclonic epilepsyM G Sweeney, S R Hammans, L W Duchen, et al.
Journal of the Peripheral Nervous System : JPNS|June 27, 2015
MFN2 deletion of exons 7 and 8: founder mutation in the UK populationAisling S Carr, James M Polke, Jacob Wilson, et al.
Brain : a Journal of Neurology|October 5, 2014
Peripheral neuropathy predicts nuclear gene defect in patients with mitochondrial ophthalmoplegiaAlejandro Horga, Robert D S Pitceathly, Julian C Blake, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 7, 2007
Multiple mitochondrial DNA deletions in monozygotic twins with OPMDM M K Muqit, A J Larner, M G Sweeney, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 31, 2012
Distal myopathy with cachexia: an unrecognised phenotype caused by dominantly-inherited mitochondrial polymerase γ mutationsRobert D S Pitceathly, Susan E Tomlinson, Iain Hargreaves, et al.
Pageof 22

Showing results (181-190 of 220) with videos related to

Sort By:
Pageof 22
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1995
Bilateral simultaneous optic neuropathy in adults: clinical, imaging, serological, and genetic studiesS P Morrissey, F X Borruat, D H Miller, et al.
Plastic and Reconstructive Surgery|July 27, 2019
Facial Transplantation for an Irreparable Central and Lower Face Injury: A Modernized Approach to a Classic ChallengeRami S Kantar, Daniel J Ceradini, Bruce E Gelb, et al.
Journal of Medical Genetics|March 8, 2011
Kearns-Sayre syndrome caused by defective R1/p53R2 assemblyRobert D S Pitceathly, Elisa Fassone, Jan-Willem Taanman, et al.
Neurobiology of Aging|January 16, 2015
Investigation of next-generation sequencing technologies as a diagnostic tool for amyotrophic lateral sclerosisSarah Morgan, Maryam Shoai, Pietro Fratta, et al.
Brain : a Journal of Neurology|February 26, 2016
In vivo impact of presynaptic calcium channel dysfunction on motor axons in episodic ataxia type 2Susan E Tomlinson, S Veronica Tan, David Burke, et al.
Journal of the Neurological Sciences|January 1, 1994
Mitochondrial DNA mutation underlying Leigh's syndrome: clinical, pathological, biochemical, and genetic studies of a patient presenting with progressive myoclonic epilepsyM G Sweeney, S R Hammans, L W Duchen, et al.
Journal of the Peripheral Nervous System : JPNS|June 27, 2015
MFN2 deletion of exons 7 and 8: founder mutation in the UK populationAisling S Carr, James M Polke, Jacob Wilson, et al.
Brain : a Journal of Neurology|October 5, 2014
Peripheral neuropathy predicts nuclear gene defect in patients with mitochondrial ophthalmoplegiaAlejandro Horga, Robert D S Pitceathly, Julian C Blake, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 7, 2007
Multiple mitochondrial DNA deletions in monozygotic twins with OPMDM M K Muqit, A J Larner, M G Sweeney, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 31, 2012
Distal myopathy with cachexia: an unrecognised phenotype caused by dominantly-inherited mitochondrial polymerase γ mutationsRobert D S Pitceathly, Susan E Tomlinson, Iain Hargreaves, et al.
Pageof 22