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Garth Nicholson

Showing results (1-10 of 67) with videos related to

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Neurology|December 25, 2002
GDAP1 mutations in CMT4: axonal and demyelinating phenotypes?: The exception "proves the rule"Garth Nicholson, Robert Ouvrier
The International Journal of Neuroscience|July 26, 2005
Age dependent penetrance of three different superoxide dismutase 1 (sod 1) mutationsArun Aggarwal, Garth Nicholson
Neuromolecular Medicine|June 16, 2006
Intermediate forms of Charcot-Marie-Tooth neuropathy: a reviewGarth Nicholson, Simon Myers
Advances in Experimental Medicine and Biology|March 13, 2010
Genotypes & sensory phenotypes in 2 new X-linked neuropathies (CMTX3 and dSMAX) and dominant CMT/HMN overlap syndromesGarth Nicholson, Marina Kennerson, Megan Brewer, et al.
Journal of the Neurological Sciences|November 18, 2004
Hereditary sensory neuropathy type 1 in a Portuguese family-electrodiagnostic and autonomic nervous system studiesRuth Geraldes, Mamede de Carvalho, Mariana Santos-Bento, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|October 1, 2016
Motor cortical dysfunction develops in spinocerebellar ataxia type 3Michelle A Farrar, Steve Vucic, Garth Nicholson, et al.
Journal of the Peripheral Nervous System : JPNS|March 14, 2019
Hereditary sensory and autonomic neuropathy type IC accompanied by upper motor neuron abnormalities and type II juxtafoveal retinal telangiectasiasJames Triplett, Garth Nicholson, Carolyn Sue, et al.
Journal of Neurodegenerative Diseases|August 29, 2015
The MFN2 V705I Variant Is Not a Disease-Causing Mutation: A Segregation Analysis in a CMT2 FamilyObaid M Albulym, Danqing Zhu, Stephen Reddel, et al.
Developmental Medicine and Child Neurology|June 6, 2003
Peripheral neuropathies of infancyJo M Wilmshurst, John D Pollard, Garth Nicholson, et al.
Seminars in Neurology|October 23, 2019
Inherited NeuropathiesAntonia S Carroll, Joshua Burns, Garth Nicholson, et al.
Pageof 7

Showing results (1-10 of 67) with videos related to

Sort By:
Pageof 7
Neurology|December 25, 2002
GDAP1 mutations in CMT4: axonal and demyelinating phenotypes?: The exception "proves the rule"Garth Nicholson, Robert Ouvrier
The International Journal of Neuroscience|July 26, 2005
Age dependent penetrance of three different superoxide dismutase 1 (sod 1) mutationsArun Aggarwal, Garth Nicholson
Neuromolecular Medicine|June 16, 2006
Intermediate forms of Charcot-Marie-Tooth neuropathy: a reviewGarth Nicholson, Simon Myers
Advances in Experimental Medicine and Biology|March 13, 2010
Genotypes & sensory phenotypes in 2 new X-linked neuropathies (CMTX3 and dSMAX) and dominant CMT/HMN overlap syndromesGarth Nicholson, Marina Kennerson, Megan Brewer, et al.
Journal of the Neurological Sciences|November 18, 2004
Hereditary sensory neuropathy type 1 in a Portuguese family-electrodiagnostic and autonomic nervous system studiesRuth Geraldes, Mamede de Carvalho, Mariana Santos-Bento, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|October 1, 2016
Motor cortical dysfunction develops in spinocerebellar ataxia type 3Michelle A Farrar, Steve Vucic, Garth Nicholson, et al.
Journal of the Peripheral Nervous System : JPNS|March 14, 2019
Hereditary sensory and autonomic neuropathy type IC accompanied by upper motor neuron abnormalities and type II juxtafoveal retinal telangiectasiasJames Triplett, Garth Nicholson, Carolyn Sue, et al.
Journal of Neurodegenerative Diseases|August 29, 2015
The MFN2 V705I Variant Is Not a Disease-Causing Mutation: A Segregation Analysis in a CMT2 FamilyObaid M Albulym, Danqing Zhu, Stephen Reddel, et al.
Developmental Medicine and Child Neurology|June 6, 2003
Peripheral neuropathies of infancyJo M Wilmshurst, John D Pollard, Garth Nicholson, et al.
Seminars in Neurology|October 23, 2019
Inherited NeuropathiesAntonia S Carroll, Joshua Burns, Garth Nicholson, et al.
Pageof 7