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Journal of Medical Genetics
|
July 5, 2003
Frequency of rare mitochondrial DNA mutations in patients with suspected Leber's hereditary optic neuropathy
R W Taylor, M S Jobling, D M Turnbull, et al.
Proceedings of the Royal Society of London. Series B, Biological Sciences
|
June 22, 1990
Local circuitry in the IMHV of the domestic chick (Gallus domesticus)
P M Bradley, B D Burns, P F Chinnery, et al.
Journal of Medical Genetics
|
April 3, 2004
Primary open angle glaucoma is associated with a specific p53 gene haplotype
T Ressiniotis, P G Griffiths, M Birch, et al.
Eye (London, England)
|
March 8, 2014
Treatment strategies for inherited optic neuropathies: past, present and future
P Yu-Wai-Man, M Votruba, A T Moore, et al.
Journal of Neurology
|
November 14, 2013
Enhanced reticulospinal output in patients with (REEP1) hereditary spastic paraplegia type 31
K M Fisher, P F Chinnery, S N Baker, et al.
Nature Genetics
|
February 1, 1997
Selective inhibition of mutant human mitochondrial DNA replication in vitro by peptide nucleic acids
R W Taylor, P F Chinnery, D M Turnbull, et al.
Methods in Molecular Medicine
|
February 22, 2012
Analysis of mitochondrial DNA mutations : point mutations
R W Taylor, R M Andrews, P F Chinnery, et al.
Eye (London, England)
|
March 9, 2000
Evaluation of bupivacaine-induced muscle regeneration in the treatment of ptosis in patients with chronic progressive external ophthalmoplegia and Kearns-Sayre syndrome
R M Andrews, P G Griffiths, P F Chinnery, et al.
American Journal of Medical Genetics
|
February 13, 2001
Leber hereditary optic neuropathy: Does heteroplasmy influence the inheritance and expression of the G11778A mitochondrial DNA mutation?
P F Chinnery, R M Andrews, D M Turnbull, et al.
Journal of Medical Genetics
|
November 13, 2008
Inherited mitochondrial optic neuropathies
P Yu-Wai-Man, P G Griffiths, G Hudson, et al.
Page
of 16
Search research articles
Search
Showing results (41-50 of 152) with videos related to
Sort By:
Page
of 16
Journal of Medical Genetics
|
July 5, 2003
Frequency of rare mitochondrial DNA mutations in patients with suspected Leber's hereditary optic neuropathy
R W Taylor, M S Jobling, D M Turnbull, et al.
Proceedings of the Royal Society of London. Series B, Biological Sciences
|
June 22, 1990
Local circuitry in the IMHV of the domestic chick (Gallus domesticus)
P M Bradley, B D Burns, P F Chinnery, et al.
Journal of Medical Genetics
|
April 3, 2004
Primary open angle glaucoma is associated with a specific p53 gene haplotype
T Ressiniotis, P G Griffiths, M Birch, et al.
Eye (London, England)
|
March 8, 2014
Treatment strategies for inherited optic neuropathies: past, present and future
P Yu-Wai-Man, M Votruba, A T Moore, et al.
Journal of Neurology
|
November 14, 2013
Enhanced reticulospinal output in patients with (REEP1) hereditary spastic paraplegia type 31
K M Fisher, P F Chinnery, S N Baker, et al.
Nature Genetics
|
February 1, 1997
Selective inhibition of mutant human mitochondrial DNA replication in vitro by peptide nucleic acids
R W Taylor, P F Chinnery, D M Turnbull, et al.
Methods in Molecular Medicine
|
February 22, 2012
Analysis of mitochondrial DNA mutations : point mutations
R W Taylor, R M Andrews, P F Chinnery, et al.
Eye (London, England)
|
March 9, 2000
Evaluation of bupivacaine-induced muscle regeneration in the treatment of ptosis in patients with chronic progressive external ophthalmoplegia and Kearns-Sayre syndrome
R M Andrews, P G Griffiths, P F Chinnery, et al.
American Journal of Medical Genetics
|
February 13, 2001
Leber hereditary optic neuropathy: Does heteroplasmy influence the inheritance and expression of the G11778A mitochondrial DNA mutation?
P F Chinnery, R M Andrews, D M Turnbull, et al.
Journal of Medical Genetics
|
November 13, 2008
Inherited mitochondrial optic neuropathies
P Yu-Wai-Man, P G Griffiths, G Hudson, et al.
Page
of 16