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Patrick F Chinnery

Showing results (181-190 of 473) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|December 7, 2010
Recessive spastic paraparesis associated with complex I deficiency due to MTHFR mutationsDeborah Bathgate, Patrick Yu-Wai-Man, Brian Webb, et al.
Molecular Genetics and Metabolism|April 15, 2014
Valproic acid triggers increased mitochondrial biogenesis in POLG-deficient fibroblastsKamil S Sitarz, Hannah R Elliott, Betül S Karaman, et al.
The Journal of Pediatrics|August 5, 2006
The mitochondrial DNA A3243A>G mutation must be an infrequent cause of Asperger syndromeLindsey Kent, Claire Lambert, Angela Pyle, et al.
Annals of Neurology|February 14, 2014
Mitochondrial DNA and traumatic brain injuryHarry Bulstrode, James A R Nicoll, Gavin Hudson, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 27, 2009
No association between common POLG1 variants and sporadic idiopathic Parkinson's diseaseGavin Hudson, Watcharee Tiangyou, Andrea Stutt, et al.
Neuromuscular Disorders : NMD|January 22, 2014
A new disease allele for the p.C30071R mutation in titin causing hereditary myopathy with early respiratory failureGerald Pfeffer, Nyamkhishig Sambuughin, Montse Olivé, et al.
Brain : a Journal of Neurology|October 19, 2010
OPA1 mutations impair mitochondrial function in both pure and complicated dominant optic atrophyPatrick Yu-Wai-Man, Michael I Trenell, Kieren G Hollingsworth, et al.
Progress in Neurobiology|May 15, 2020
Epigenetic regulation in the pathophysiology of Lewy body dementiaLeonidas Chouliaras, Gautham S Kumar, Alan J Thomas, et al.
Brain : a Journal of Neurology|October 31, 2007
Does mitochondrial DNA predispose to neuromyelitis optica (Devic's disease)?Gavin Hudson, Catherine Mowbray, Joanna L Elson, et al.
The British Journal of Ophthalmology|January 25, 2014
Abnormal retinal thickening is a common feature among patients with ARSACS-related phenotypesPatrick Yu-Wai-Man, Angela Pyle, Helen Griffin, et al.
Pageof 48

Showing results (181-190 of 473) with videos related to

Sort By:
Pageof 48
Journal of Neurology, Neurosurgery, and Psychiatry|December 7, 2010
Recessive spastic paraparesis associated with complex I deficiency due to MTHFR mutationsDeborah Bathgate, Patrick Yu-Wai-Man, Brian Webb, et al.
Molecular Genetics and Metabolism|April 15, 2014
Valproic acid triggers increased mitochondrial biogenesis in POLG-deficient fibroblastsKamil S Sitarz, Hannah R Elliott, Betül S Karaman, et al.
The Journal of Pediatrics|August 5, 2006
The mitochondrial DNA A3243A>G mutation must be an infrequent cause of Asperger syndromeLindsey Kent, Claire Lambert, Angela Pyle, et al.
Annals of Neurology|February 14, 2014
Mitochondrial DNA and traumatic brain injuryHarry Bulstrode, James A R Nicoll, Gavin Hudson, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 27, 2009
No association between common POLG1 variants and sporadic idiopathic Parkinson's diseaseGavin Hudson, Watcharee Tiangyou, Andrea Stutt, et al.
Neuromuscular Disorders : NMD|January 22, 2014
A new disease allele for the p.C30071R mutation in titin causing hereditary myopathy with early respiratory failureGerald Pfeffer, Nyamkhishig Sambuughin, Montse Olivé, et al.
Brain : a Journal of Neurology|October 19, 2010
OPA1 mutations impair mitochondrial function in both pure and complicated dominant optic atrophyPatrick Yu-Wai-Man, Michael I Trenell, Kieren G Hollingsworth, et al.
Progress in Neurobiology|May 15, 2020
Epigenetic regulation in the pathophysiology of Lewy body dementiaLeonidas Chouliaras, Gautham S Kumar, Alan J Thomas, et al.
Brain : a Journal of Neurology|October 31, 2007
Does mitochondrial DNA predispose to neuromyelitis optica (Devic's disease)?Gavin Hudson, Catherine Mowbray, Joanna L Elson, et al.
The British Journal of Ophthalmology|January 25, 2014
Abnormal retinal thickening is a common feature among patients with ARSACS-related phenotypesPatrick Yu-Wai-Man, Angela Pyle, Helen Griffin, et al.
Pageof 48