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Patrick F Chinnery

Showing results (171-180 of 473) with videos related to

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Annals of Neurology|September 5, 2002
Normokalemic periodic paralysis revisited: does it exist?Patrick F Chinnery, Timothy J Walls, Michael G Hanna, et al.
Neuromuscular Disorders : NMD|August 9, 2005
Subclinical semitendinosus and obturator externus involvement defines an autosomal dominant myopathy with early respiratory failureDaniel Birchall, Maja von der Hagen, David Bates, et al.
Neurology|November 8, 2013
Clinical features of MS associated with Leber hereditary optic neuropathy mtDNA mutationsGerald Pfeffer, Ailbhe Burke, Patrick Yu-Wai-Man, et al.
Plos Genetics|April 26, 2014
The challenges of mitochondrial replacementPatrick F Chinnery, Lyndsey Craven, Shoukhrat Mitalipov, et al.
Acta Ophthalmologica|December 12, 2007
Investigation of auditory dysfunction in Leber hereditary optic neuropathyPatrick Yu-Wai-Man, Clive Elliott, Philip G Griffiths, et al.
Science Advances|October 25, 2023
High-throughput single-cell analysis reveals progressive mitochondrial DNA mosaicism throughout lifeAngelos Glynos, Lyuba V Bozhilova, Michele Frison, et al.
Human Molecular Genetics|October 10, 2023
CHCHD10 mutations induce tissue-specific mitochondrial DNA deletions with a distinct signatureMario K Shammas, Yu Nie, Alexandra Gilsrud, et al.
Neurobiology of Aging|July 29, 2011
No evidence of substantia nigra telomere shortening in Parkinson's diseaseGavin Hudson, David Faini, Andrea Stutt, et al.
JAMA Neurology|October 25, 2016
A Woman With Intellectual Disability, Amenorrhoea, Seizures, and Balance ProblemsAlastair J C Hughes, Hannah E Steele, Angela Pyle, et al.
Brain : a Journal of Neurology|October 16, 2008
Clinical features and natural history of neuroferritinopathy caused by the 458dupA FTL mutationDavid Devos, P Jissendi Tchofo, Isabelle Vuillaume, et al.
Pageof 48

Showing results (171-180 of 473) with videos related to

Sort By:
Pageof 48
Annals of Neurology|September 5, 2002
Normokalemic periodic paralysis revisited: does it exist?Patrick F Chinnery, Timothy J Walls, Michael G Hanna, et al.
Neuromuscular Disorders : NMD|August 9, 2005
Subclinical semitendinosus and obturator externus involvement defines an autosomal dominant myopathy with early respiratory failureDaniel Birchall, Maja von der Hagen, David Bates, et al.
Neurology|November 8, 2013
Clinical features of MS associated with Leber hereditary optic neuropathy mtDNA mutationsGerald Pfeffer, Ailbhe Burke, Patrick Yu-Wai-Man, et al.
Plos Genetics|April 26, 2014
The challenges of mitochondrial replacementPatrick F Chinnery, Lyndsey Craven, Shoukhrat Mitalipov, et al.
Acta Ophthalmologica|December 12, 2007
Investigation of auditory dysfunction in Leber hereditary optic neuropathyPatrick Yu-Wai-Man, Clive Elliott, Philip G Griffiths, et al.
Science Advances|October 25, 2023
High-throughput single-cell analysis reveals progressive mitochondrial DNA mosaicism throughout lifeAngelos Glynos, Lyuba V Bozhilova, Michele Frison, et al.
Human Molecular Genetics|October 10, 2023
CHCHD10 mutations induce tissue-specific mitochondrial DNA deletions with a distinct signatureMario K Shammas, Yu Nie, Alexandra Gilsrud, et al.
Neurobiology of Aging|July 29, 2011
No evidence of substantia nigra telomere shortening in Parkinson's diseaseGavin Hudson, David Faini, Andrea Stutt, et al.
JAMA Neurology|October 25, 2016
A Woman With Intellectual Disability, Amenorrhoea, Seizures, and Balance ProblemsAlastair J C Hughes, Hannah E Steele, Angela Pyle, et al.
Brain : a Journal of Neurology|October 16, 2008
Clinical features and natural history of neuroferritinopathy caused by the 458dupA FTL mutationDavid Devos, P Jissendi Tchofo, Isabelle Vuillaume, et al.
Pageof 48