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Patrick F Chinnery

Showing results (241-250 of 473) with videos related to

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Neuromuscular Disorders : NMD|April 27, 2020
Chronic pain is common in mitochondrial diseaseJelle van den Ameele, Joshua Fuge, Robert D S Pitceathly, et al.
Scientific Reports|February 21, 2019
Mitochondrial Haplogroup and the Risk of Acute Kidney Injury Following Cardiac Bypass SurgeryNigel S Kanagasundaram, Simon V Baudouin, Sarah Rowling, et al.
Annals of Neurology|September 22, 2007
Prevalence of mitochondrial DNA disease in adultsAndrew M Schaefer, Robert McFarland, Emma L Blakely, et al.
Neurology. Genetics|September 29, 2017
De novo <i>CTBP1</i> variant is associated with decreased mitochondrial respiratory chain activitiesEwen W Sommerville, Charlotte L Alston, Angela Pyle, et al.
Nucleic Acids Research|July 24, 2002
Detection and quantification of mitochondrial DNA deletions in individual cells by real-time PCRLangping He, Patrick F Chinnery, Steve E Durham, et al.
Archives of Neurology|July 4, 2012
Prominent sensorimotor neuropathy due to SACS mutations revealed by whole-exome sequencingAngela Pyle, Helen Griffin, Patrick Yu-Wai-Man, et al.
Hepatology (Baltimore, Md.)|November 2, 2010
Polymerase γ gene POLG determines the risk of sodium valproate-induced liver toxicityJoanna D Stewart, Rita Horvath, Enrico Baruffini, et al.
Mitochondrion|May 22, 2012
Unique mitochondrial DNA in highly inbred feral cattleGavin Hudson, Ian Wilson, Brendan I A Payne, et al.
JIMD Reports|August 31, 2016
Lethal Neonatal LTBL Associated with Biallelic EARS2 Variants: Case Report and Review of the Reported Neuroradiological FeaturesRenata Oliveira, Ewen W Sommerville, Kyle Thompson, et al.
Molecular Vision|January 5, 2011
Variation in OPA1 does not explain the incomplete penetrance of Leber hereditary optic neuropathyGavin Hudson, Patrick Yu-Wai-Man, Phillip G Griffiths, et al.
Pageof 48

Showing results (241-250 of 473) with videos related to

Sort By:
Pageof 48
Neuromuscular Disorders : NMD|April 27, 2020
Chronic pain is common in mitochondrial diseaseJelle van den Ameele, Joshua Fuge, Robert D S Pitceathly, et al.
Scientific Reports|February 21, 2019
Mitochondrial Haplogroup and the Risk of Acute Kidney Injury Following Cardiac Bypass SurgeryNigel S Kanagasundaram, Simon V Baudouin, Sarah Rowling, et al.
Annals of Neurology|September 22, 2007
Prevalence of mitochondrial DNA disease in adultsAndrew M Schaefer, Robert McFarland, Emma L Blakely, et al.
Neurology. Genetics|September 29, 2017
De novo <i>CTBP1</i> variant is associated with decreased mitochondrial respiratory chain activitiesEwen W Sommerville, Charlotte L Alston, Angela Pyle, et al.
Nucleic Acids Research|July 24, 2002
Detection and quantification of mitochondrial DNA deletions in individual cells by real-time PCRLangping He, Patrick F Chinnery, Steve E Durham, et al.
Archives of Neurology|July 4, 2012
Prominent sensorimotor neuropathy due to SACS mutations revealed by whole-exome sequencingAngela Pyle, Helen Griffin, Patrick Yu-Wai-Man, et al.
Hepatology (Baltimore, Md.)|November 2, 2010
Polymerase γ gene POLG determines the risk of sodium valproate-induced liver toxicityJoanna D Stewart, Rita Horvath, Enrico Baruffini, et al.
Mitochondrion|May 22, 2012
Unique mitochondrial DNA in highly inbred feral cattleGavin Hudson, Ian Wilson, Brendan I A Payne, et al.
JIMD Reports|August 31, 2016
Lethal Neonatal LTBL Associated with Biallelic EARS2 Variants: Case Report and Review of the Reported Neuroradiological FeaturesRenata Oliveira, Ewen W Sommerville, Kyle Thompson, et al.
Molecular Vision|January 5, 2011
Variation in OPA1 does not explain the incomplete penetrance of Leber hereditary optic neuropathyGavin Hudson, Patrick Yu-Wai-Man, Phillip G Griffiths, et al.
Pageof 48