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P Yu-Wai-Man

Showing results (11-20 of 22) with videos related to

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Journal of Medical Genetics|April 3, 2004
Mitochondrial DNA haplogroup distribution within Leber hereditary optic neuropathy pedigreesP Yu-Wai-Man, N Howell, D A Mackey, et al.
Neurology|September 16, 2011
Subclinical multisystem neurologic disease in "pure" OPA1 autosomal dominant optic atrophyM R Baker, K M Fisher, R G Whittaker, et al.
Neurology|June 27, 2002
NDUFA-1 is not a nuclear modifier gene in Leber hereditary optic neuropathyP Yu-Wai-Man, D T Brown, M S Wehnert, et al.
Journal of Medical Genetics|July 8, 2009
OPA1 increases the risk of normal but not high tension glaucomaP Yu-Wai-Man, J D Stewart, G Hudson, et al.
Journal of Medical Genetics|February 3, 2009
Genomic rearrangements in OPA1 are frequent in patients with autosomal dominant optic atrophyN Fuhrmann, M V Alavi, P Bitoun, et al.
Scientific Reports|October 15, 2021
A mutant wfs1 zebrafish model of Wolfram syndrome manifesting visual dysfunction and developmental delayG Cairns, F Burté, R Price, et al.
Mitochondrion|July 22, 2017
The pattern of retinal ganglion cell dysfunction in Leber hereditary optic neuropathyA Majander, A G Robson, C João, et al.
Cell Death & Disease|November 30, 2024
OPA1 and disease-causing mutants perturb mitochondrial nucleoid distributionJ Macuada, I Molina-Riquelme, G Vidal, et al.
Neurology|November 26, 2008
OPA1 in multiple mitochondrial DNA deletion disordersJ D Stewart, G Hudson, P Yu-Wai-Man, et al.
Brain : a Journal of Neurology|February 8, 2013
Persistence of the treatment effect of idebenone in Leber's hereditary optic neuropathyT Klopstock, G Metz, P Yu-Wai-Man, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Journal of Medical Genetics|April 3, 2004
Mitochondrial DNA haplogroup distribution within Leber hereditary optic neuropathy pedigreesP Yu-Wai-Man, N Howell, D A Mackey, et al.
Neurology|September 16, 2011
Subclinical multisystem neurologic disease in "pure" OPA1 autosomal dominant optic atrophyM R Baker, K M Fisher, R G Whittaker, et al.
Neurology|June 27, 2002
NDUFA-1 is not a nuclear modifier gene in Leber hereditary optic neuropathyP Yu-Wai-Man, D T Brown, M S Wehnert, et al.
Journal of Medical Genetics|July 8, 2009
OPA1 increases the risk of normal but not high tension glaucomaP Yu-Wai-Man, J D Stewart, G Hudson, et al.
Journal of Medical Genetics|February 3, 2009
Genomic rearrangements in OPA1 are frequent in patients with autosomal dominant optic atrophyN Fuhrmann, M V Alavi, P Bitoun, et al.
Scientific Reports|October 15, 2021
A mutant wfs1 zebrafish model of Wolfram syndrome manifesting visual dysfunction and developmental delayG Cairns, F Burté, R Price, et al.
Mitochondrion|July 22, 2017
The pattern of retinal ganglion cell dysfunction in Leber hereditary optic neuropathyA Majander, A G Robson, C João, et al.
Cell Death & Disease|November 30, 2024
OPA1 and disease-causing mutants perturb mitochondrial nucleoid distributionJ Macuada, I Molina-Riquelme, G Vidal, et al.
Neurology|November 26, 2008
OPA1 in multiple mitochondrial DNA deletion disordersJ D Stewart, G Hudson, P Yu-Wai-Man, et al.
Brain : a Journal of Neurology|February 8, 2013
Persistence of the treatment effect of idebenone in Leber's hereditary optic neuropathyT Klopstock, G Metz, P Yu-Wai-Man, et al.
Pageof 3