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Patrick F Chinnery

Showing results (211-220 of 473) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|September 25, 2004
Spectrum of movement disorders in neuroferritinopathyDouglas E Crompton, Patrick F Chinnery, David Bates, et al.
Experimental Neurology|October 10, 2009
Subtle neurological and metabolic abnormalities in an Opa1 mouse model of autosomal dominant optic atrophyMarcel V Alavi, Nico Fuhrmann, Huu Phuc Nguyen, et al.
Journal of Neurology|December 15, 2012
The neurological and ophthalmological manifestations of SPG4-related hereditary spastic paraplegiaGrant Guthrie, Gerald Pfeffer, Maura Bailie, et al.
Neurology|April 3, 2015
Clinical heterogeneity of primary familial brain calcification due to a novel mutation in PDGFBMichael J Keogh, Angela Pyle, Daniyal Daud, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|July 13, 2023
Multisystem pathology in McLeod syndromeKatherine R Schon, Dominic G O'Donovan, Mayen Briggs, et al.
Annals of Neurology|September 8, 2015
Reduced cerebrospinal fluid mitochondrial DNA is a biomarker for early-stage Parkinson's diseaseAngela Pyle, Rebecca Brennan, Marzena Kurzawa-Akanbi, et al.
European Journal of Human Genetics : EJHG|June 17, 2004
Noninvasive diagnosis of the 3243A > G mitochondrial DNA mutation using urinary epithelial cellsMartina T McDonnell, Andrew M Schaefer, Emma L Blakely, et al.
European Neurology|July 11, 2009
Lower limb radiology of distal myopathy due to the S60F myotilin mutationAlisdair McNeill, Daniel Birchall, Volker Straub, et al.
Neuroscience Letters|May 25, 2010
Genetic variation of CHRNA4 does not modulate attention in Parkinson's diseaseGavin Hudson, Andrea Stutt, Martin Eccles, et al.
Behavioural Neurology|August 18, 2010
The contribution of the cerebellum to cognition in Spinocerebellar Ataxia Type 6Freya E Cooper, Manon Grube, Kelly J Elsegood, et al.
Pageof 48

Showing results (211-220 of 473) with videos related to

Sort By:
Pageof 48
Movement Disorders : Official Journal of the Movement Disorder Society|September 25, 2004
Spectrum of movement disorders in neuroferritinopathyDouglas E Crompton, Patrick F Chinnery, David Bates, et al.
Experimental Neurology|October 10, 2009
Subtle neurological and metabolic abnormalities in an Opa1 mouse model of autosomal dominant optic atrophyMarcel V Alavi, Nico Fuhrmann, Huu Phuc Nguyen, et al.
Journal of Neurology|December 15, 2012
The neurological and ophthalmological manifestations of SPG4-related hereditary spastic paraplegiaGrant Guthrie, Gerald Pfeffer, Maura Bailie, et al.
Neurology|April 3, 2015
Clinical heterogeneity of primary familial brain calcification due to a novel mutation in PDGFBMichael J Keogh, Angela Pyle, Daniyal Daud, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|July 13, 2023
Multisystem pathology in McLeod syndromeKatherine R Schon, Dominic G O'Donovan, Mayen Briggs, et al.
Annals of Neurology|September 8, 2015
Reduced cerebrospinal fluid mitochondrial DNA is a biomarker for early-stage Parkinson's diseaseAngela Pyle, Rebecca Brennan, Marzena Kurzawa-Akanbi, et al.
European Journal of Human Genetics : EJHG|June 17, 2004
Noninvasive diagnosis of the 3243A > G mitochondrial DNA mutation using urinary epithelial cellsMartina T McDonnell, Andrew M Schaefer, Emma L Blakely, et al.
European Neurology|July 11, 2009
Lower limb radiology of distal myopathy due to the S60F myotilin mutationAlisdair McNeill, Daniel Birchall, Volker Straub, et al.
Neuroscience Letters|May 25, 2010
Genetic variation of CHRNA4 does not modulate attention in Parkinson's diseaseGavin Hudson, Andrea Stutt, Martin Eccles, et al.
Behavioural Neurology|August 18, 2010
The contribution of the cerebellum to cognition in Spinocerebellar Ataxia Type 6Freya E Cooper, Manon Grube, Kelly J Elsegood, et al.
Pageof 48