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Garth Nicholson

Showing results (21-30 of 67) with videos related to

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Muscle & Nerve|August 22, 2012
A family with 2 X-linked disorders: Charcot-Marie-Tooth disease and hemophilia ANortina Shahrizaila, Khean Jin Goh, Azlina Ahmad-Annuar, et al.
Neurology|June 10, 2016
Novel motor phenotypes in patients with VRK1 mutations without pontocerebellar hypoplasiaMarion Stoll, Hooiling Teoh, James Lee, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 31, 2012
"Dancing feet dyskinesias": a clue to parkin gene mutationsFlorence C F Chang, Prachi Mehta, Brianada Koentjoro, et al.
Disability and Rehabilitation|November 4, 2017
Body composition and its association with physical performance, quality of life, and clinical indictors in Charcot-Marie-Tooth disease: a pilot studyDaniel Hackett, Daniel Roberts-Clarke, Nidhi Jain, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|April 23, 2008
Association study on glutathione S-transferase omega 1 and 2 and familial ALSElsmarieke van de Giessen, Isabella Fogh, Sumana Gopinath, et al.
Human Molecular Genetics|April 3, 2023
A humanized yeast model reveals dominant-negative properties of neuropathy-associated alanyl-tRNA synthetase mutationsRebecca Meyer-Schuman, Sheila Marte, Tyler J Smith, et al.
Annals of Neurology|March 3, 2004
Tau haplotypes regulate transcription and are associated with Parkinson's diseaseJohn B J Kwok, Erdahl T Teber, Clement Loy, et al.
The Journal of Biological Chemistry|January 26, 2010
Hereditary sensory neuropathy type 1 is caused by the accumulation of two neurotoxic sphingolipidsAnke Penno, Mary M Reilly, Henry Houlden, et al.
Disease Models & Mechanisms|January 24, 2020
Modelling the pathogenesis of X-linked distal hereditary motor neuropathy using patient-derived iPSCsGonzalo Perez-Siles, Anthony Cutrupi, Melina Ellis, et al.
Human Molecular Genetics|June 19, 2015
Homozygous mutations in MFN2 cause multiple symmetric lipomatosis associated with neuropathySarah L Sawyer, Andy Cheuk-Him Ng, A Micheil Innes, et al.
Pageof 7

Showing results (21-30 of 67) with videos related to

Sort By:
Pageof 7
Muscle & Nerve|August 22, 2012
A family with 2 X-linked disorders: Charcot-Marie-Tooth disease and hemophilia ANortina Shahrizaila, Khean Jin Goh, Azlina Ahmad-Annuar, et al.
Neurology|June 10, 2016
Novel motor phenotypes in patients with VRK1 mutations without pontocerebellar hypoplasiaMarion Stoll, Hooiling Teoh, James Lee, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 31, 2012
"Dancing feet dyskinesias": a clue to parkin gene mutationsFlorence C F Chang, Prachi Mehta, Brianada Koentjoro, et al.
Disability and Rehabilitation|November 4, 2017
Body composition and its association with physical performance, quality of life, and clinical indictors in Charcot-Marie-Tooth disease: a pilot studyDaniel Hackett, Daniel Roberts-Clarke, Nidhi Jain, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|April 23, 2008
Association study on glutathione S-transferase omega 1 and 2 and familial ALSElsmarieke van de Giessen, Isabella Fogh, Sumana Gopinath, et al.
Human Molecular Genetics|April 3, 2023
A humanized yeast model reveals dominant-negative properties of neuropathy-associated alanyl-tRNA synthetase mutationsRebecca Meyer-Schuman, Sheila Marte, Tyler J Smith, et al.
Annals of Neurology|March 3, 2004
Tau haplotypes regulate transcription and are associated with Parkinson's diseaseJohn B J Kwok, Erdahl T Teber, Clement Loy, et al.
The Journal of Biological Chemistry|January 26, 2010
Hereditary sensory neuropathy type 1 is caused by the accumulation of two neurotoxic sphingolipidsAnke Penno, Mary M Reilly, Henry Houlden, et al.
Disease Models & Mechanisms|January 24, 2020
Modelling the pathogenesis of X-linked distal hereditary motor neuropathy using patient-derived iPSCsGonzalo Perez-Siles, Anthony Cutrupi, Melina Ellis, et al.
Human Molecular Genetics|June 19, 2015
Homozygous mutations in MFN2 cause multiple symmetric lipomatosis associated with neuropathySarah L Sawyer, Andy Cheuk-Him Ng, A Micheil Innes, et al.
Pageof 7