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P Chinnery

Showing results (1-10 of 8) with videos related to

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The British Journal of Radiology|July 28, 2005
Radiological characterization of spinocerebellar ataxia type 6D Butteriss, P Chinnery, D Birchall
The Cochrane Database of Systematic Reviews|January 27, 2006
Treatment for mitochondrial disordersP Chinnery, K Majamaa, D Turnbull, et al.
Acta Paediatrica (Oslo, Norway : 1992)|January 6, 2009
Abnormal growth in mitochondrial diseaseS Wolny, R McFarland, P Chinnery, et al.
European Journal of Neurology|August 26, 2006
Task force guidelines handbook: EFNS guidelines on diagnosis and management of fatty acid mitochondrial disordersC Angelini, A Federico, H Reichmann, 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.
Cell Death Discovery|June 9, 2016
Loss of function of <i>Ywhah</i> in mice induces deafness and cochlear outer hair cells' degenerationL Buret, G Rebillard, E Brun, et al.
Nature Communications|January 10, 2015
Mutations in PNPLA6 are linked to photoreceptor degeneration and various forms of childhood blindnessS Kmoch, J Majewski, V Ramamurthy, et al.
Neurology|December 14, 2005
BDNF genetic variants are associated with onset age of familial Parkinson disease: GenePD StudyS Karamohamed, J C Latourelle, B A Racette, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
The British Journal of Radiology|July 28, 2005
Radiological characterization of spinocerebellar ataxia type 6D Butteriss, P Chinnery, D Birchall
The Cochrane Database of Systematic Reviews|January 27, 2006
Treatment for mitochondrial disordersP Chinnery, K Majamaa, D Turnbull, et al.
Acta Paediatrica (Oslo, Norway : 1992)|January 6, 2009
Abnormal growth in mitochondrial diseaseS Wolny, R McFarland, P Chinnery, et al.
European Journal of Neurology|August 26, 2006
Task force guidelines handbook: EFNS guidelines on diagnosis and management of fatty acid mitochondrial disordersC Angelini, A Federico, H Reichmann, 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.
Cell Death Discovery|June 9, 2016
Loss of function of <i>Ywhah</i> in mice induces deafness and cochlear outer hair cells' degenerationL Buret, G Rebillard, E Brun, et al.
Nature Communications|January 10, 2015
Mutations in PNPLA6 are linked to photoreceptor degeneration and various forms of childhood blindnessS Kmoch, J Majewski, V Ramamurthy, et al.
Neurology|December 14, 2005
BDNF genetic variants are associated with onset age of familial Parkinson disease: GenePD StudyS Karamohamed, J C Latourelle, B A Racette, et al.
Pageof 1