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Kamil S Sitarz

Showing results (1-10 of 8) with videos related to

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Current Neurology and Neuroscience Reports|March 7, 2012
Disorders of the optic nerve in mitochondrial cytopathies: new ideas on pathogenesis and therapeutic targetsKamil S Sitarz, Patrick F Chinnery, Patrick Yu-Wai-Man
Molecular Genetics and Metabolism|April 15, 2014
Valproic acid triggers increased mitochondrial biogenesis in POLG-deficient fibroblastsKamil S Sitarz, Hannah R Elliott, Betül S Karaman, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|August 11, 2011
Genetic variations within the OPA1 gene are not associated with neuromyelitis opticaKamil S Sitarz, Patrick Yu-Wai-Man, Gavin Hudson, et al.
Human Molecular Genetics|May 21, 2010
OPA1 mutations cause cytochrome c oxidase deficiency due to loss of wild-type mtDNA moleculesPatrick Yu-Wai-Man, Kamil S Sitarz, David C Samuels, et al.
Brain : a Journal of Neurology|April 12, 2012
MFN2 mutations cause compensatory mitochondrial DNA proliferationKamil S Sitarz, Patrick Yu-Wai-Man, Angela Pyle, et al.
Neurology|September 21, 2012
OPA1 mutations induce mtDNA proliferation in leukocytes of patients with dominant optic atrophyKamil S Sitarz, Gitte J Almind, Rita Horvath, et al.
Biochimica Et Biophysica Acta|December 9, 2010
POLG mutations cause decreased mitochondrial DNA repopulation rates following induced depletion in human fibroblastsJoanna D Stewart, Susanne Schoeler, Kamil S Sitarz, et al.
Neurology|December 16, 2016
Dysregulated mitophagy and mitochondrial organization in optic atrophy due to OPA1 mutationsChunyan Liao, Neil Ashley, Alan Diot, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Current Neurology and Neuroscience Reports|March 7, 2012
Disorders of the optic nerve in mitochondrial cytopathies: new ideas on pathogenesis and therapeutic targetsKamil S Sitarz, Patrick F Chinnery, Patrick Yu-Wai-Man
Molecular Genetics and Metabolism|April 15, 2014
Valproic acid triggers increased mitochondrial biogenesis in POLG-deficient fibroblastsKamil S Sitarz, Hannah R Elliott, Betül S Karaman, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|August 11, 2011
Genetic variations within the OPA1 gene are not associated with neuromyelitis opticaKamil S Sitarz, Patrick Yu-Wai-Man, Gavin Hudson, et al.
Human Molecular Genetics|May 21, 2010
OPA1 mutations cause cytochrome c oxidase deficiency due to loss of wild-type mtDNA moleculesPatrick Yu-Wai-Man, Kamil S Sitarz, David C Samuels, et al.
Brain : a Journal of Neurology|April 12, 2012
MFN2 mutations cause compensatory mitochondrial DNA proliferationKamil S Sitarz, Patrick Yu-Wai-Man, Angela Pyle, et al.
Neurology|September 21, 2012
OPA1 mutations induce mtDNA proliferation in leukocytes of patients with dominant optic atrophyKamil S Sitarz, Gitte J Almind, Rita Horvath, et al.
Biochimica Et Biophysica Acta|December 9, 2010
POLG mutations cause decreased mitochondrial DNA repopulation rates following induced depletion in human fibroblastsJoanna D Stewart, Susanne Schoeler, Kamil S Sitarz, et al.
Neurology|December 16, 2016
Dysregulated mitophagy and mitochondrial organization in optic atrophy due to OPA1 mutationsChunyan Liao, Neil Ashley, Alan Diot, et al.
Pageof 1