Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

O A Ross

Showing results (21-30 of 36) with videos related to

Pageof 4
Sort By:
Neurology|October 27, 2004
PINK1 (PARK6) associated Parkinson disease in IrelandD G Healy, P M Abou-Sleiman, J M Gibson, et al.
Neurology|January 26, 2007
Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplicationJ Fuchs, C Nilsson, J Kachergus, et al.
Neuropathology and Applied Neurobiology|November 19, 2016
Clinicopathologic heterogeneity in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) due to microtubule-associated protein tau (MAPT) p.P301L mutation, including a patient with globular glial tauopathyP Tacik, M Sanchez-Contreras, M DeTure, et al.
European Journal of Neurology|May 29, 2009
GRN 3'UTR+78 C>T is not associated with risk for Parkinson's diseaseB Jasinska-Myga, C Wider, G Opala, et al.
European Journal of Neurology|June 3, 2015
Low density lipoprotein receptor related protein 1 and 6 gene variants and ischaemic stroke riskA M Harriott, M G Heckman, S Rayaprolu, et al.
Neurology|February 16, 2011
MAPT H1 haplotype is a risk factor for essential tremor and multiple system atrophyC Vilariño-Güell, A I Soto-Ortolaza, A Rajput, et al.
Neurology|May 11, 2011
A family with Parkinsonism, essential tremor, restless legs syndrome, and depressionA Puschmann, R F Pfeiffer, A J Stoessl, et al.
European Journal of Neurology|November 17, 2009
Association of the MAPT locus with Parkinson's diseaseC Wider, C Vilariño-Güell, B Jasinska-Myga, et al.
Neurology|December 22, 2010
An independent replication of PARK16 in Asian samplesC Vilariño-Güell, O A Ross, J O Aasly, et al.
European Journal of Neurology|December 17, 2010
SNCA, MAPT, and GSK3B in Parkinson disease: a gene-gene interaction studyC Wider, C Vilariño-Güell, M G Heckman, et al.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
Neurology|October 27, 2004
PINK1 (PARK6) associated Parkinson disease in IrelandD G Healy, P M Abou-Sleiman, J M Gibson, et al.
Neurology|January 26, 2007
Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplicationJ Fuchs, C Nilsson, J Kachergus, et al.
Neuropathology and Applied Neurobiology|November 19, 2016
Clinicopathologic heterogeneity in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) due to microtubule-associated protein tau (MAPT) p.P301L mutation, including a patient with globular glial tauopathyP Tacik, M Sanchez-Contreras, M DeTure, et al.
European Journal of Neurology|May 29, 2009
GRN 3'UTR+78 C>T is not associated with risk for Parkinson's diseaseB Jasinska-Myga, C Wider, G Opala, et al.
European Journal of Neurology|June 3, 2015
Low density lipoprotein receptor related protein 1 and 6 gene variants and ischaemic stroke riskA M Harriott, M G Heckman, S Rayaprolu, et al.
Neurology|February 16, 2011
MAPT H1 haplotype is a risk factor for essential tremor and multiple system atrophyC Vilariño-Güell, A I Soto-Ortolaza, A Rajput, et al.
Neurology|May 11, 2011
A family with Parkinsonism, essential tremor, restless legs syndrome, and depressionA Puschmann, R F Pfeiffer, A J Stoessl, et al.
European Journal of Neurology|November 17, 2009
Association of the MAPT locus with Parkinson's diseaseC Wider, C Vilariño-Güell, B Jasinska-Myga, et al.
Neurology|December 22, 2010
An independent replication of PARK16 in Asian samplesC Vilariño-Güell, O A Ross, J O Aasly, et al.
European Journal of Neurology|December 17, 2010
SNCA, MAPT, and GSK3B in Parkinson disease: a gene-gene interaction studyC Wider, C Vilariño-Güell, M G Heckman, et al.
Pageof 4