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Daniel G Healy

Showing results (31-40 of 50) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|February 1, 2014
Temporal discrimination, a cervical dystonia endophenotype: penetrance and functional correlatesOkka Kimmich, Anna Molloy, Robert Whelan, et al.
Frontiers in Neurology|May 8, 2014
Cervical dystonia: a disorder of the midbrain network for covert attentional orientingMichael Hutchinson, Tadashi Isa, Anna Molloy, et al.
Human Molecular Genetics|June 28, 2012
G2019S leucine-rich repeat kinase 2 causes uncoupling protein-mediated mitochondrial depolarizationTatiana D Papkovskaia, Kai-Yin Chau, Francisco Inesta-Vaquera, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 16, 2006
NR4A2 genetic variation in sporadic Parkinson's disease: a genewide approachDaniel G Healy, Patrick M Abou-Sleiman, Kourosh R Ahmadi, et al.
Annals of Neurology|September 7, 2004
The gene responsible for PARK6 Parkinson's disease, PINK1, does not influence common forms of parkinsonismDaniel G Healy, Patrick M Abou-Sleiman, Kourosh R Ahmadi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 26, 2014
An evaluation of the role of environmental factors in the disease penetrance of cervical dystoniaAnna Molloy, Okka Kimmich, Laura Williams, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 5, 2009
Evidence for pre and postsynaptic nigrostriatal dysfunction in the fragile X tremor-ataxia syndromeDaniel G Healy, Susan Bressman, John Dickson, et al.
Parkinsonism & Related Disorders|October 29, 2020
The "round the houses" sign and "zig-zag" sign in progressive supranuclear palsy and other conditionsConor Fearon, Robert Field, Eoghan Donlon, et al.
Annals of Neurology|September 14, 2006
A heterozygous effect for PINK1 mutations in Parkinson's disease?Patrick M Abou-Sleiman, Miratul M K Muqit, Neil Q McDonald, et al.
Lancet (London, England)|February 1, 2005
A common LRRK2 mutation in idiopathic Parkinson's diseaseWilliam P Gilks, Patrick M Abou-Sleiman, Sonia Gandhi, et al.
Pageof 5

Showing results (31-40 of 50) with videos related to

Sort By:
Pageof 5
Movement Disorders : Official Journal of the Movement Disorder Society|February 1, 2014
Temporal discrimination, a cervical dystonia endophenotype: penetrance and functional correlatesOkka Kimmich, Anna Molloy, Robert Whelan, et al.
Frontiers in Neurology|May 8, 2014
Cervical dystonia: a disorder of the midbrain network for covert attentional orientingMichael Hutchinson, Tadashi Isa, Anna Molloy, et al.
Human Molecular Genetics|June 28, 2012
G2019S leucine-rich repeat kinase 2 causes uncoupling protein-mediated mitochondrial depolarizationTatiana D Papkovskaia, Kai-Yin Chau, Francisco Inesta-Vaquera, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 16, 2006
NR4A2 genetic variation in sporadic Parkinson's disease: a genewide approachDaniel G Healy, Patrick M Abou-Sleiman, Kourosh R Ahmadi, et al.
Annals of Neurology|September 7, 2004
The gene responsible for PARK6 Parkinson's disease, PINK1, does not influence common forms of parkinsonismDaniel G Healy, Patrick M Abou-Sleiman, Kourosh R Ahmadi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 26, 2014
An evaluation of the role of environmental factors in the disease penetrance of cervical dystoniaAnna Molloy, Okka Kimmich, Laura Williams, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 5, 2009
Evidence for pre and postsynaptic nigrostriatal dysfunction in the fragile X tremor-ataxia syndromeDaniel G Healy, Susan Bressman, John Dickson, et al.
Parkinsonism & Related Disorders|October 29, 2020
The "round the houses" sign and "zig-zag" sign in progressive supranuclear palsy and other conditionsConor Fearon, Robert Field, Eoghan Donlon, et al.
Annals of Neurology|September 14, 2006
A heterozygous effect for PINK1 mutations in Parkinson's disease?Patrick M Abou-Sleiman, Miratul M K Muqit, Neil Q McDonald, et al.
Lancet (London, England)|February 1, 2005
A common LRRK2 mutation in idiopathic Parkinson's diseaseWilliam P Gilks, Patrick M Abou-Sleiman, Sonia Gandhi, et al.
Pageof 5