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C Paisán

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

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European Journal of Neurology|December 18, 2008
R632W mutation in PLA2G6 segregates with dystonia-parkinsonism in a consanguineous Iranian familyF Sina, S Shojaee, E Elahi, et al.
Clinical Genetics|April 25, 2017
A novel TRPA1 variant is associated with carbamazepine-responsive cramp-fasciculation syndromeM J Nirenberg, R Chaouni, T M Biller, et al.
Clinical Genetics|January 3, 2013
Rapid disease progression in adult-onset mitochondrial membrane protein-associated neurodegenerationO Dogu, C E Krebs, H Kaleagasi, et al.
Neuroscience Letters|October 19, 2004
Mitochondrial polymporphisms in Parkinson's DiseaseD Otaegui, C Paisán, A Sáenz, et al.
Neurobiology of Aging|April 5, 2008
Whole genome analysis in a consanguineous family with early onset Alzheimer's diseaseJ Clarimón, R Djaldetti, A Lleó, et al.
Neuroscience Letters|August 15, 2006
Apolipoprotein E epsilon4 allele in familial and sporadic Parkinson's diseaseL Blázquez, D Otaegui, A Sáenz, et al.
Journal of Neurology|October 1, 2014
Compound heterozygous PNPLA6 mutations cause Boucher-Neuhäuser syndrome with late-onset ataxiaA Deik, B Johannes, J C Rucker, et al.
Neurology|September 15, 2005
LRRK2 gene in Parkinson disease: mutation analysis and case control association studyC Paisán-Ruíz, A E Lang, T Kawarai, et al.
Journal of Medical Genetics|February 10, 2006
Testing association between LRRK2 and Parkinson's disease and investigating linkage disequilibriumC Paisán-Ruíz, E W Evans, S Jain, et al.
Brain : a Journal of Neurology|February 4, 2005
LGMD2A: genotype-phenotype correlations based on a large mutational survey on the calpain 3 geneA Sáenz, F Leturcq, A M Cobo, et al.
Pageof 1

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

Sort By:
Pageof 1
European Journal of Neurology|December 18, 2008
R632W mutation in PLA2G6 segregates with dystonia-parkinsonism in a consanguineous Iranian familyF Sina, S Shojaee, E Elahi, et al.
Clinical Genetics|April 25, 2017
A novel TRPA1 variant is associated with carbamazepine-responsive cramp-fasciculation syndromeM J Nirenberg, R Chaouni, T M Biller, et al.
Clinical Genetics|January 3, 2013
Rapid disease progression in adult-onset mitochondrial membrane protein-associated neurodegenerationO Dogu, C E Krebs, H Kaleagasi, et al.
Neuroscience Letters|October 19, 2004
Mitochondrial polymporphisms in Parkinson's DiseaseD Otaegui, C Paisán, A Sáenz, et al.
Neurobiology of Aging|April 5, 2008
Whole genome analysis in a consanguineous family with early onset Alzheimer's diseaseJ Clarimón, R Djaldetti, A Lleó, et al.
Neuroscience Letters|August 15, 2006
Apolipoprotein E epsilon4 allele in familial and sporadic Parkinson's diseaseL Blázquez, D Otaegui, A Sáenz, et al.
Journal of Neurology|October 1, 2014
Compound heterozygous PNPLA6 mutations cause Boucher-Neuhäuser syndrome with late-onset ataxiaA Deik, B Johannes, J C Rucker, et al.
Neurology|September 15, 2005
LRRK2 gene in Parkinson disease: mutation analysis and case control association studyC Paisán-Ruíz, A E Lang, T Kawarai, et al.
Journal of Medical Genetics|February 10, 2006
Testing association between LRRK2 and Parkinson's disease and investigating linkage disequilibriumC Paisán-Ruíz, E W Evans, S Jain, et al.
Brain : a Journal of Neurology|February 4, 2005
LGMD2A: genotype-phenotype correlations based on a large mutational survey on the calpain 3 geneA Sáenz, F Leturcq, A M Cobo, et al.
Pageof 1