Showing results (251-260 of 370) with videos related to
Sort By:
Pageof 37
European Heart Journal. Cardiovascular Imaging|November 7, 2012
Concentric hypertrophic remodelling and subendocardial dysfunction in mitochondrial DNA point mutation carriersMatthew G D Bates, Kieren G Hollingsworth, Jane H Newman, et al.Neurology. Genetics|April 12, 2016
Respiratory chain deficiency in nonmitochondrial diseaseAngela Pyle, Helen J Nightingale, Helen Griffin, et al.Science (New York, N.Y.)|October 9, 2025
Ubiquitin-mediated mitophagy regulates the inheritance of mitochondrial DNA mutationsMichele Frison, Brandon S Lockey, Yu Nie, et al.Neurology|April 22, 2021
[<sup>11</sup>C]PK11195-PET Brain Imaging of the Mitochondrial Translocator Protein in Mitochondrial DiseaseJelle van den Ameele, Young T Hong, Roido Manavaki, et al.Human Mutation|February 27, 2016
MSeqDR: A Centralized Knowledge Repository and Bioinformatics Web Resource to Facilitate Genomic Investigations in Mitochondrial DiseaseLishuang Shen, Maria Angela Diroma, Michael Gonzalez, et al.American Journal of Human Genetics|December 29, 2005
Identification of an X-chromosomal locus and haplotype modulating the phenotype of a mitochondrial DNA disorderGavin Hudson, Sharon Keers, Patrick Yu-Wai-Man, et al.JAMA Neurology|November 25, 2014
Clonal expansion of secondary mitochondrial DNA deletions associated with spinocerebellar ataxia type 28Gráinne S Gorman, Gerald Pfeffer, Helen Griffin, et al.Journal of Neurology|September 4, 2014
ANO10 mutations cause ataxia and coenzyme Q₁₀ deficiencyAndrea Balreira, Veronika Boczonadi, Emanuele Barca, et al.American Journal of Human Genetics|May 3, 2016
Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain DeficienciesMetodi D Metodiev, Kyle Thompson, Charlotte L Alston, et al.Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 2011
Adult-onset cerebellar ataxia due to mutations in CABC1/ADCK3Rita Horvath, Birgit Czermin, Sweena Gulati, et al.Pageof 37