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Journal of Neurology, Neurosurgery, and Psychiatry
|
September 4, 2009
A comparative study of LRRK2, PINK1 and genetically undefined familial Parkinson's disease
Kenya 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 Africa
Barbara 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 parkinsonism
Stanley B Prusiner, Amanda L Woerman, Daniel A Mordes, et al.
Molecular Psychiatry
|
December 25, 2008
Genome-wide association study of recurrent major depressive disorder in two European case-control cohorts
P Muglia, F Tozzi, N W Galwey, et al.
The Lancet. Neurology
|
June 10, 2008
LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic study
Mary M Hulihan, Lianna Ishihara-Paul, Jennifer Kachergus, et al.
Human Mutation
|
December 17, 2008
ATP13A2 variability in Parkinson disease
Carles Vilariño-Güell, Alexandra I Soto, Sarah J Lincoln, 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 mutation
Antonis Ververis, Rana Dajani, Pantelitsa Koutsou, 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 Cohort
Yujia Zhao, Anushree Ray, Karin Broberg, et al.
Frontiers in Public Health
|
December 6, 2021
Health, Lifestyle, and Psycho-Social Determinants of Poor Sleep Quality During the Early Phase of the COVID-19 Pandemic: A Focus on UK Older Adults Deemed Clinically Extremely Vulnerable
Chinedu T Udeh-Momoh, Tamlyn Watermeyer, Shireen Sindi, et al.
Neurology
|
August 8, 2008
PINK1 mutations and parkinsonism
L Ishihara-Paul, M M Hulihan, J Kachergus, et al.
Page
of 19
Search research articles
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Showing results (151-160 of 181) with videos related to
Sort By:
Page
of 19
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 4, 2009
A comparative study of LRRK2, PINK1 and genetically undefined familial Parkinson's disease
Kenya 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 Africa
Barbara 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 parkinsonism
Stanley B Prusiner, Amanda L Woerman, Daniel A Mordes, et al.
Molecular Psychiatry
|
December 25, 2008
Genome-wide association study of recurrent major depressive disorder in two European case-control cohorts
P Muglia, F Tozzi, N W Galwey, et al.
The Lancet. Neurology
|
June 10, 2008
LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic study
Mary M Hulihan, Lianna Ishihara-Paul, Jennifer Kachergus, et al.
Human Mutation
|
December 17, 2008
ATP13A2 variability in Parkinson disease
Carles Vilariño-Güell, Alexandra I Soto, Sarah J Lincoln, 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 mutation
Antonis Ververis, Rana Dajani, Pantelitsa Koutsou, 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 Cohort
Yujia Zhao, Anushree Ray, Karin Broberg, et al.
Frontiers in Public Health
|
December 6, 2021
Health, Lifestyle, and Psycho-Social Determinants of Poor Sleep Quality During the Early Phase of the COVID-19 Pandemic: A Focus on UK Older Adults Deemed Clinically Extremely Vulnerable
Chinedu T Udeh-Momoh, Tamlyn Watermeyer, Shireen Sindi, et al.
Neurology
|
August 8, 2008
PINK1 mutations and parkinsonism
L Ishihara-Paul, M M Hulihan, J Kachergus, et al.
Page
of 19