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European Journal of Human Genetics : EJHG|April 12, 2007
Abundance of the POLG disease mutations in Europe, Australia, New Zealand, and the United States explained by single ancient European foundersAnna H Hakonen, Guido Davidzon, Renato Salemi, et al.
European Journal of Nutrition|September 11, 2025
Bone and mineral metabolism in 2-7-year-old Finnish children and their caregivers following vegan, vegetarian, and omnivorous dietsSuvi T Itkonen, Topi Hovinen, Elina Kettunen, et al.
Circulation|December 2, 2025
Mitochondrial Genetics in Cardiovascular Health and Disease: A Scientific Statement From the American Heart AssociationJessica L Fetterman, Patrick F Chinnery, Rebecca McClellan, et al.
Cell Metabolism|August 3, 2017
mTORC1 Regulates Mitochondrial Integrated Stress Response and Mitochondrial Myopathy ProgressionNahid A Khan, Joni Nikkanen, Shuichi Yatsuga, et al.
Neurology. Genetics|July 9, 2020
Genetic background of ataxia in children younger than 5 years in FinlandErika Ignatius, Pirjo Isohanni, Max Pohjanpelto, et al.
Journal of Community Genetics|April 6, 2020
Attitudes towards genetic testing and information: does parenthood shape the views?Antti Saastamoinen, Virva Hyttinen, Mika Kortelainen, et al.
Human Molecular Genetics|February 20, 2010
Ketogenic diet slows down mitochondrial myopathy progression in miceSofia Ahola-Erkkilä, Christopher J Carroll, Katja Peltola-Mjösund, et al.
Neurology|July 20, 2014
Mitochondrial EFTs defects in juvenile-onset Leigh disease, ataxia, neuropathy, and optic atrophySofia Ahola, Pirjo Isohanni, Liliya Euro, et al.
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