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Gavin Hudson

Showing results (81-90 of 100) with videos related to

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Human Molecular Genetics|January 8, 2016
Mitochondrial DNA sequence characteristics modulate the size of the genetic bottleneckIan J Wilson, Phillipa J Carling, Charlotte L Alston, et al.
Plos Genetics|March 8, 2017
Mutations in mitochondrial DNA causing tubulointerstitial kidney diseaseThomas M Connor, Simon Hoer, Andrew Mallett, et al.
Brain : a Journal of Neurology|December 28, 2010
A founder mutation in Anoctamin 5 is a major cause of limb-girdle muscular dystrophyDebbie Hicks, Anna Sarkozy, Nuria Muelas, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 18, 2012
A new phenotype of brain iron accumulation with dystonia, optic atrophy, and peripheral neuropathyRita Horvath, Elke Holinski-Feder, Vivienne C M Neeve, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 2, 2022
GBA and APOE Impact Cognitive Decline in Parkinson's Disease: A 10-Year Population-Based StudyAleksandra A Szwedo, Ingvild Dalen, Kenn Freddy Pedersen, et al.
Brain : a Journal of Neurology|April 20, 2006
Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma geneRita Horvath, Gavin Hudson, Gianfrancesco Ferrari, et al.
Neurology|December 24, 2013
Characterizing mild cognitive impairment in incident Parkinson disease: the ICICLE-PD studyAlison J Yarnall, David P Breen, Gordon W Duncan, et al.
Annals of the Rheumatic Diseases|September 18, 2012
No evidence of an association between mitochondrial DNA variants and osteoarthritis in 7393 cases and 5122 controlsGavin Hudson, Kalliope Panoutsopoulou, Ian Wilson, et al.
Scientific Reports|May 18, 2026
Mavodelpar in patients with primary mitochondrial myopathy: a phase 1 trialRenae J Stefanetti, Chiara Pizzamiglio, Alasdair P Blain, et al.
American Journal of Human Genetics|August 2, 2007
Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup backgroundGavin Hudson, Valerio Carelli, Liesbeth Spruijt, et al.
Pageof 10

Showing results (81-90 of 100) with videos related to

Sort By:
Pageof 10
Human Molecular Genetics|January 8, 2016
Mitochondrial DNA sequence characteristics modulate the size of the genetic bottleneckIan J Wilson, Phillipa J Carling, Charlotte L Alston, et al.
Plos Genetics|March 8, 2017
Mutations in mitochondrial DNA causing tubulointerstitial kidney diseaseThomas M Connor, Simon Hoer, Andrew Mallett, et al.
Brain : a Journal of Neurology|December 28, 2010
A founder mutation in Anoctamin 5 is a major cause of limb-girdle muscular dystrophyDebbie Hicks, Anna Sarkozy, Nuria Muelas, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 18, 2012
A new phenotype of brain iron accumulation with dystonia, optic atrophy, and peripheral neuropathyRita Horvath, Elke Holinski-Feder, Vivienne C M Neeve, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 2, 2022
GBA and APOE Impact Cognitive Decline in Parkinson's Disease: A 10-Year Population-Based StudyAleksandra A Szwedo, Ingvild Dalen, Kenn Freddy Pedersen, et al.
Brain : a Journal of Neurology|April 20, 2006
Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma geneRita Horvath, Gavin Hudson, Gianfrancesco Ferrari, et al.
Neurology|December 24, 2013
Characterizing mild cognitive impairment in incident Parkinson disease: the ICICLE-PD studyAlison J Yarnall, David P Breen, Gordon W Duncan, et al.
Annals of the Rheumatic Diseases|September 18, 2012
No evidence of an association between mitochondrial DNA variants and osteoarthritis in 7393 cases and 5122 controlsGavin Hudson, Kalliope Panoutsopoulou, Ian Wilson, et al.
Scientific Reports|May 18, 2026
Mavodelpar in patients with primary mitochondrial myopathy: a phase 1 trialRenae J Stefanetti, Chiara Pizzamiglio, Alasdair P Blain, et al.
American Journal of Human Genetics|August 2, 2007
Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup backgroundGavin Hudson, Valerio Carelli, Liesbeth Spruijt, et al.
Pageof 10