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Lefkos T Middleton

Showing results (31-40 of 57) with videos related to

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American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 2, 2010
A genomewide linkage study on suicidality in major depressive disorder confirms evidence for linkage to 2p12Amy W Butler, Gerome Breen, Federica Tozzi, et al.
American Journal of Human Genetics|April 12, 2003
Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type VAnthony Antonellis, Rachel E Ellsworth, Nyamkhishig Sambuughin, et al.
The American Journal of Cardiology|January 12, 2005
Relation between atherogenic dyslipidemia and the Adult Treatment Program-III definition of metabolic syndrome (Genetic Epidemiology of Metabolic Syndrome Project)Diego F Wyszynski, Dawn M Waterworth, Philip J Barter, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 4, 2009
A comparative study of LRRK2, PINK1 and genetically undefined familial Parkinson's diseaseKenya Nishioka, Mounir Kefi, Barbara Jasinska-Myga, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 20, 2010
Comprehensive sequencing of the LRRK2 gene in patients with familial Parkinson's disease from North AfricaBarbara Jasinska-Myga, Jennifer Kachergus, Carles Vilariño-Güell, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 2, 2015
Evidence for α-synuclein prions causing multiple system atrophy in humans with parkinsonismStanley B Prusiner, Amanda L Woerman, Daniel A Mordes, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 7, 2023
Prediagnostic Blood Metal Levels and the Risk of Parkinson's Disease: A Large European Prospective CohortYujia Zhao, Anushree Ray, Karin Broberg, et al.
Journal of Medical Genetics|September 13, 2019
Distal hereditary motor neuronopathy of the Jerash type is caused by a novel <i>SIGMAR1</i> c.500A>T missense mutationAntonis Ververis, Rana Dajani, Pantelitsa Koutsou, et al.
The Lancet. Neurology|June 10, 2008
LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic studyMary M Hulihan, Lianna Ishihara-Paul, Jennifer Kachergus, et al.
Human Mutation|December 17, 2008
ATP13A2 variability in Parkinson diseaseCarles Vilariño-Güell, Alexandra I Soto, Sarah J Lincoln, et al.
Pageof 6

Showing results (31-40 of 57) with videos related to

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Pageof 6
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 2, 2010
A genomewide linkage study on suicidality in major depressive disorder confirms evidence for linkage to 2p12Amy W Butler, Gerome Breen, Federica Tozzi, et al.
American Journal of Human Genetics|April 12, 2003
Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type VAnthony Antonellis, Rachel E Ellsworth, Nyamkhishig Sambuughin, et al.
The American Journal of Cardiology|January 12, 2005
Relation between atherogenic dyslipidemia and the Adult Treatment Program-III definition of metabolic syndrome (Genetic Epidemiology of Metabolic Syndrome Project)Diego F Wyszynski, Dawn M Waterworth, Philip J Barter, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 4, 2009
A comparative study of LRRK2, PINK1 and genetically undefined familial Parkinson's diseaseKenya Nishioka, Mounir Kefi, Barbara Jasinska-Myga, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 20, 2010
Comprehensive sequencing of the LRRK2 gene in patients with familial Parkinson's disease from North AfricaBarbara Jasinska-Myga, Jennifer Kachergus, Carles Vilariño-Güell, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 2, 2015
Evidence for α-synuclein prions causing multiple system atrophy in humans with parkinsonismStanley B Prusiner, Amanda L Woerman, Daniel A Mordes, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 7, 2023
Prediagnostic Blood Metal Levels and the Risk of Parkinson's Disease: A Large European Prospective CohortYujia Zhao, Anushree Ray, Karin Broberg, et al.
Journal of Medical Genetics|September 13, 2019
Distal hereditary motor neuronopathy of the Jerash type is caused by a novel <i>SIGMAR1</i> c.500A>T missense mutationAntonis Ververis, Rana Dajani, Pantelitsa Koutsou, et al.
The Lancet. Neurology|June 10, 2008
LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic studyMary M Hulihan, Lianna Ishihara-Paul, Jennifer Kachergus, et al.
Human Mutation|December 17, 2008
ATP13A2 variability in Parkinson diseaseCarles Vilariño-Güell, Alexandra I Soto, Sarah J Lincoln, et al.
Pageof 6