Endurance training and detraining in mitochondrial myopathies due to single large-scale mtDNA deletions

By Taivassalo Tanja   Gardner Julie L.   Schaefer Andrew M.   Newman Jane   Barron Martin J.   Haller Ronald G.   Turnbull Douglass M.  

Brain, Vol. 129, Iss. 12, 2006-12 ,pp. : 3391-3401

Oxford University Press

Access to resources Recommend Favorite

Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance

By Hudson Gavin  

Brain, Vol. 131, Iss. 2, 2008-02 ,pp. : 329-337

Oxford University Press

Access to resources Recommend Favorite

mtDNA disease for the neurologist

By Nesbitt Victoria   Whittaker Roger G   Turnbull Douglass M   McFarland Robert   Taylor Robert W  

Future Neurology, Vol. 6, Iss. 1, 2011-01 ,pp. : 63-80

Future Medicine

Access to resources Recommend Favorite

Thymidine kinase 2 defects can cause multi-tissue mtDNA depletion syndrome

By Götz Alexandra  

Brain, Vol. 131, Iss. 11, 2008-11 ,pp. : 2841-2850

Oxford University Press

Access to resources Recommend Favorite

No evidence for paternal inheritance of mtDNA in patients with sporadic mtDNA mutations

By Schwartz M.   Vissing J.  

Journal of the Neurological Sciences, Vol. 218, Iss. 1, 2004-03 ,pp. : 99-101

Elsevier

Access to resources Recommend Favorite