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P F Chinnery

Showing results (91-100 of 152) with videos related to

Pageof 16
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Neurology. Genetics|November 11, 2016
Novel <i>HSPB1</i> mutation causes both motor neuronopathy and distal myopathyD J Lewis-Smith, J Duff, A Pyle, et al.
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.
Journal of Medical Genetics|May 15, 2003
Neuroferritinopathy in a French family with late onset dominant dystoniaP F Chinnery, A R J Curtis, C Fey, 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.
Annals of Neurology|September 1, 1996
MELAS associated with a mutation in the valine transfer RNA gene of mitochondrial DNAR W Taylor, P F Chinnery, F Haldane, et al.
Gut|December 15, 2000
Mitochondrial enteropathy: the primary pathology may not be within the gastrointestinal tractP F Chinnery, S Jones, L Sviland, 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|January 13, 2010
A novel FTL insertion causing neuroferritinopathyS Batey, I Vuillaume, D Devos, et al.
Journal of Medical Genetics|February 6, 2004
Mitochondrial DNA deletion in "identical" twin brothersE L Blakely, L He, R W Taylor, et al.
Archives of Disease in Childhood|January 23, 2008
Reversible valproate hepatotoxicity due to mutations in mitochondrial DNA polymerase gamma (POLG1)R McFarland, G Hudson, R W Taylor, et al.
Pageof 16

Showing results (91-100 of 152) with videos related to

Sort By:
Pageof 16
Neurology. Genetics|November 11, 2016
Novel <i>HSPB1</i> mutation causes both motor neuronopathy and distal myopathyD J Lewis-Smith, J Duff, A Pyle, et al.
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.
Journal of Medical Genetics|May 15, 2003
Neuroferritinopathy in a French family with late onset dominant dystoniaP F Chinnery, A R J Curtis, C Fey, 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.
Annals of Neurology|September 1, 1996
MELAS associated with a mutation in the valine transfer RNA gene of mitochondrial DNAR W Taylor, P F Chinnery, F Haldane, et al.
Gut|December 15, 2000
Mitochondrial enteropathy: the primary pathology may not be within the gastrointestinal tractP F Chinnery, S Jones, L Sviland, 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|January 13, 2010
A novel FTL insertion causing neuroferritinopathyS Batey, I Vuillaume, D Devos, et al.
Journal of Medical Genetics|February 6, 2004
Mitochondrial DNA deletion in "identical" twin brothersE L Blakely, L He, R W Taylor, et al.
Archives of Disease in Childhood|January 23, 2008
Reversible valproate hepatotoxicity due to mutations in mitochondrial DNA polymerase gamma (POLG1)R McFarland, G Hudson, R W Taylor, et al.
Pageof 16