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Laurence A Bindoff

Showing results (1-10 of 130) with videos related to

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Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|March 23, 2011
[When the most common isn't the explanation]Laurence A Bindoff
Epilepsia|October 5, 2011
Mitochondrial function and pathology in status epilepticusLaurence A Bindoff
Neurology|March 26, 2008
Melas associated with mutations in the polg1 geneCharalampos Tzoulis, Laurence A Bindoff
Journal of Parkinson'S Disease|August 14, 2013
A novel compound heterozygous tyrosine hydroxylase mutation (p.R441P) with complex phenotypeKristoffer Haugarvoll, Laurence A Bindoff
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|March 28, 2002
[Dopa-responsive dystonia--a hereditary dystonia easy to treat]Elisabeth Farbu, Laurence A Bindoff
Brain : a Journal of Neurology|October 16, 2012
Acute mitochondrial encephalopathy reflects neuronal energy failure irrespective of which genome the genetic defect affectsCharalampos Tzoulis, Laurence A Bindoff
Stroke|December 20, 2008
Serial diffusion imaging in a case of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodesCharalampos Tzoulis, Laurence A Bindoff
Human Mutation|October 16, 2012
MT-ND5 mutation causing exercise intolerance displays intercellular heteroplasmy and rapid shifts between generationsPetter Schandl Sanaker, Laurence A Bindoff
Handbook of Clinical Neurology|June 13, 2018
Mitochondrial ataxiasHilary J Vernon, Laurence A Bindoff
Epilepsia|September 6, 2012
Mitochondrial diseases and epilepsyLaurence A Bindoff, Bernt A Engelsen
Pageof 13

Showing results (1-10 of 130) with videos related to

Sort By:
Pageof 13
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|March 23, 2011
[When the most common isn't the explanation]Laurence A Bindoff
Epilepsia|October 5, 2011
Mitochondrial function and pathology in status epilepticusLaurence A Bindoff
Neurology|March 26, 2008
Melas associated with mutations in the polg1 geneCharalampos Tzoulis, Laurence A Bindoff
Journal of Parkinson'S Disease|August 14, 2013
A novel compound heterozygous tyrosine hydroxylase mutation (p.R441P) with complex phenotypeKristoffer Haugarvoll, Laurence A Bindoff
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|March 28, 2002
[Dopa-responsive dystonia--a hereditary dystonia easy to treat]Elisabeth Farbu, Laurence A Bindoff
Brain : a Journal of Neurology|October 16, 2012
Acute mitochondrial encephalopathy reflects neuronal energy failure irrespective of which genome the genetic defect affectsCharalampos Tzoulis, Laurence A Bindoff
Stroke|December 20, 2008
Serial diffusion imaging in a case of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodesCharalampos Tzoulis, Laurence A Bindoff
Human Mutation|October 16, 2012
MT-ND5 mutation causing exercise intolerance displays intercellular heteroplasmy and rapid shifts between generationsPetter Schandl Sanaker, Laurence A Bindoff
Handbook of Clinical Neurology|June 13, 2018
Mitochondrial ataxiasHilary J Vernon, Laurence A Bindoff
Epilepsia|September 6, 2012
Mitochondrial diseases and epilepsyLaurence A Bindoff, Bernt A Engelsen
Pageof 13