Showing results (21-30 of 97) with videos related to
Sort By:
Pageof 10
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.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.Journal of Neurology|July 14, 2020
Behr syndrome and hypertrophic cardiomyopathy in a family with a novel UCHL1 deletionGrace McMacken, Hanns Lochmüller, Boglarka Bansagi, et al.EMBO Reports|August 17, 2023
Feasibility and impact of haplogroup matching for mitochondrial replacement treatmentYuko Takeda, Louise Hyslop, Meenakshi Choudhary, et al.Neurology. Genetics|September 29, 2017
De novo CTBP1 variant is associated with decreased mitochondrial respiratory chain activitiesEwen W Sommerville, Charlotte L Alston, Angela Pyle, 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.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.Journal of Neurogenetics|November 5, 2013
Late-onset sacsinopathy diagnosed by exome sequencing and comparative genomic hybridizationAngela Pyle, Helen Griffin, Jennifer Duff, et al.Lancet (London, England)|December 20, 2005
Mitochondrial DNA and survival after sepsis: a prospective studySimon V Baudouin, David Saunders, Watcharee Tiangyou, et al.Movement Disorders : Official Journal of the Movement Disorder Society|April 11, 2017
metabolic profiling of Parkinson's disease and mild cognitive impairmentFlorence Burté, David Houghton, Hannah Lowes, et al.Pageof 10