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Coro Paisán-Ruiz

Showing results (1-10 of 41) with videos related to

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Human Mutation|May 28, 2009
LRRK2 gene variation and its contribution to Parkinson diseaseCoro Paisán-Ruiz
Neurology|November 3, 2010
Common pathogenic pathways in melanoma and Parkinson diseaseCoro Paisán-Ruiz, Henry Houlden
Frontiers in Genetics|May 18, 2012
The use of next-generation sequencing in movement disordersCatharine E Krebs, Coro Paisán-Ruiz
Journal of Clinical Neurology (Seoul, Korea)|July 23, 2011
Thinning of the corpus callosum and cerebellar atrophy is correlated with phenotypic severity in a family with spastic paraplegia type 11Sanjeev Rajakulendran, Coro Paisán-Ruiz, Henry Houlden
Molecular Neurobiology|January 19, 2018
Pla2g6 Deficiency in Zebrafish Leads to Dopaminergic Cell Death, Axonal Degeneration, Increased β-Synuclein Expression, and Defects in Brain Functions and PathwaysElena Sánchez, Luis J Azcona, Coro Paisán-Ruiz
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 23, 2009
Homozygosity mapping through whole genome analysis identifies a COL18A1 mutation in an Indian family presenting with an autosomal recessive neurological disorderCoro Paisán-Ruiz, Geoff Scopes, Philip Lee, et al.
Journal of Parkinson'S Disease|August 14, 2013
LRRK2: cause, risk, and mechanismCoro Paisán-Ruiz, Patrick A Lewis, Andrew B Singleton
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|July 22, 2015
PLA2G6-associated Dystonia-Parkinsonism: Case Report and Literature ReviewSiamak Karkheiran, Gholam Ali Shahidi, Ruth H Walker, et al.
Annals of Human Genetics|June 4, 2009
Parkinson's disease and low frequency alleles found together throughout LRRK2Coro Paisán-Ruiz, Nicole Washecka, Priti Nath, et al.
NPJ Genomic Medicine|November 11, 2017
Whole genome sequencing identifies a novel homozygous exon deletion in the <i>NT5C2</i> gene in a family with intellectual disability and spastic paraplegiaHossein Darvish, Luis J Azcona, Abbas Tafakhori, et al.
Pageof 5

Showing results (1-10 of 41) with videos related to

Sort By:
Pageof 5
Human Mutation|May 28, 2009
LRRK2 gene variation and its contribution to Parkinson diseaseCoro Paisán-Ruiz
Neurology|November 3, 2010
Common pathogenic pathways in melanoma and Parkinson diseaseCoro Paisán-Ruiz, Henry Houlden
Frontiers in Genetics|May 18, 2012
The use of next-generation sequencing in movement disordersCatharine E Krebs, Coro Paisán-Ruiz
Journal of Clinical Neurology (Seoul, Korea)|July 23, 2011
Thinning of the corpus callosum and cerebellar atrophy is correlated with phenotypic severity in a family with spastic paraplegia type 11Sanjeev Rajakulendran, Coro Paisán-Ruiz, Henry Houlden
Molecular Neurobiology|January 19, 2018
Pla2g6 Deficiency in Zebrafish Leads to Dopaminergic Cell Death, Axonal Degeneration, Increased β-Synuclein Expression, and Defects in Brain Functions and PathwaysElena Sánchez, Luis J Azcona, Coro Paisán-Ruiz
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 23, 2009
Homozygosity mapping through whole genome analysis identifies a COL18A1 mutation in an Indian family presenting with an autosomal recessive neurological disorderCoro Paisán-Ruiz, Geoff Scopes, Philip Lee, et al.
Journal of Parkinson'S Disease|August 14, 2013
LRRK2: cause, risk, and mechanismCoro Paisán-Ruiz, Patrick A Lewis, Andrew B Singleton
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|July 22, 2015
PLA2G6-associated Dystonia-Parkinsonism: Case Report and Literature ReviewSiamak Karkheiran, Gholam Ali Shahidi, Ruth H Walker, et al.
Annals of Human Genetics|June 4, 2009
Parkinson's disease and low frequency alleles found together throughout LRRK2Coro Paisán-Ruiz, Nicole Washecka, Priti Nath, et al.
NPJ Genomic Medicine|November 11, 2017
Whole genome sequencing identifies a novel homozygous exon deletion in the <i>NT5C2</i> gene in a family with intellectual disability and spastic paraplegiaHossein Darvish, Luis J Azcona, Abbas Tafakhori, et al.
Pageof 5