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Patrick F Chinnery

Showing results (151-160 of 473) with videos related to

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Acta Neuropathologica|April 30, 2022
Heteroplasmic mitochondrial DNA mutations in frontotemporal lobar degenerationYu Nie, Alexander Murley, Zoe Golder, et al.
International Journal of Epidemiology|January 31, 2012
Epigenetics, epidemiology and mitochondrial DNA diseasesPatrick F Chinnery, Hannah R Elliott, Gavin Hudson, et al.
Molecular Vision|January 18, 2008
X-Inactivation patterns in females harboring mtDNA mutations that cause Leber hereditary optic neuropathyGavin Hudson, Valerio Carelli, Rita Horvath, et al.
Plos One|May 14, 2013
Raised intraocular pressure as a potential risk factor for visual loss in Leber Hereditary Optic NeuropathyAnais Thouin, Philip G Griffiths, Gavin Hudson, et al.
Acta Ophthalmologica|March 5, 2013
Visual and psychological morbidity among patients with autosomal dominant optic atrophyMaura Bailie, Marcela Votruba, Philip G Griffiths, et al.
Neurology|July 10, 2013
Clinical reasoning: a 39-year-old man with abdominal crampsStephan R Jaiser, Mark R Baker, Roger G Whittaker, et al.
Neuromuscular Disorders : NMD|March 29, 2005
A novel ANT1 gene mutation with probable germline mosaicism in autosomal dominant progressive external ophthalmoplegiaMarcus Deschauer, Gavin Hudson, Tobias Müller, et al.
Trends in Genetics : TIG|July 18, 2020
Mitochondrial Diseases: A Diagnostic RevolutionKatherine R Schon, Thiloka Ratnaike, Jelle van den Ameele, et al.
Intensive Care Medicine|March 13, 2010
Fall in circulating mononuclear cell mitochondrial DNA content in human sepsisAngela Pyle, David J Burn, Charlotte Gordon, et al.
Biochimica Et Biophysica Acta|July 9, 2004
Abnormal cardiac energetics in patients carrying the A3243G mtDNA mutation measured in vivo using phosphorus MR spectroscopyRaffaele Lodi, Bheeshma Rajagopalan, Andrew M Blamire, et al.
Pageof 48

Showing results (151-160 of 473) with videos related to

Sort By:
Pageof 48
Acta Neuropathologica|April 30, 2022
Heteroplasmic mitochondrial DNA mutations in frontotemporal lobar degenerationYu Nie, Alexander Murley, Zoe Golder, et al.
International Journal of Epidemiology|January 31, 2012
Epigenetics, epidemiology and mitochondrial DNA diseasesPatrick F Chinnery, Hannah R Elliott, Gavin Hudson, et al.
Molecular Vision|January 18, 2008
X-Inactivation patterns in females harboring mtDNA mutations that cause Leber hereditary optic neuropathyGavin Hudson, Valerio Carelli, Rita Horvath, et al.
Plos One|May 14, 2013
Raised intraocular pressure as a potential risk factor for visual loss in Leber Hereditary Optic NeuropathyAnais Thouin, Philip G Griffiths, Gavin Hudson, et al.
Acta Ophthalmologica|March 5, 2013
Visual and psychological morbidity among patients with autosomal dominant optic atrophyMaura Bailie, Marcela Votruba, Philip G Griffiths, et al.
Neurology|July 10, 2013
Clinical reasoning: a 39-year-old man with abdominal crampsStephan R Jaiser, Mark R Baker, Roger G Whittaker, et al.
Neuromuscular Disorders : NMD|March 29, 2005
A novel ANT1 gene mutation with probable germline mosaicism in autosomal dominant progressive external ophthalmoplegiaMarcus Deschauer, Gavin Hudson, Tobias Müller, et al.
Trends in Genetics : TIG|July 18, 2020
Mitochondrial Diseases: A Diagnostic RevolutionKatherine R Schon, Thiloka Ratnaike, Jelle van den Ameele, et al.
Intensive Care Medicine|March 13, 2010
Fall in circulating mononuclear cell mitochondrial DNA content in human sepsisAngela Pyle, David J Burn, Charlotte Gordon, et al.
Biochimica Et Biophysica Acta|July 9, 2004
Abnormal cardiac energetics in patients carrying the A3243G mtDNA mutation measured in vivo using phosphorus MR spectroscopyRaffaele Lodi, Bheeshma Rajagopalan, Andrew M Blamire, et al.
Pageof 48