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Patrick F. Chinnery

Showing results (131-140 of 370) with videos related to

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Human Molecular Genetics|July 2, 2013
Altered 2-thiouridylation impairs mitochondrial translation in reversible infantile respiratory chain deficiencyVeronika Boczonadi, Paul M Smith, Angela Pyle, et al.
Plos Genetics|May 15, 2015
Extreme-Depth Re-sequencing of Mitochondrial DNA Finds No Evidence of Paternal Transmission in HumansAngela Pyle, Gavin Hudson, Ian J Wilson, et al.
Muscle & Nerve|November 26, 2003
Late-onset mitochondrial disorder with electromyographic evidence of myotoniaMathew L P Howse, Theresa M Wardell, Christopher J Fisher, et al.
Neurology|August 12, 2016
Cardiac involvement in hereditary myopathy with early respiratory failure: A cohort studyHannah E Steele, Elizabeth Harris, Rita Barresi, et al.
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.
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.
Pageof 37

Showing results (131-140 of 370) with videos related to

Sort By:
Pageof 37
Human Molecular Genetics|July 2, 2013
Altered 2-thiouridylation impairs mitochondrial translation in reversible infantile respiratory chain deficiencyVeronika Boczonadi, Paul M Smith, Angela Pyle, et al.
Plos Genetics|May 15, 2015
Extreme-Depth Re-sequencing of Mitochondrial DNA Finds No Evidence of Paternal Transmission in HumansAngela Pyle, Gavin Hudson, Ian J Wilson, et al.
Muscle & Nerve|November 26, 2003
Late-onset mitochondrial disorder with electromyographic evidence of myotoniaMathew L P Howse, Theresa M Wardell, Christopher J Fisher, et al.
Neurology|August 12, 2016
Cardiac involvement in hereditary myopathy with early respiratory failure: A cohort studyHannah E Steele, Elizabeth Harris, Rita Barresi, et al.
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.
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.
Pageof 37