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

Alexandra I Soto

Showing results (1-10 of 108) with videos related to

Pageof 11
Sort By:
Parkinsonism & Related Disorders|September 29, 2015
Genetic susceptibility variants in parkinsonismAlexandra I Soto-Ortolaza, Owen A Ross
Brain : a Journal of Neurology|July 14, 2023
PTPA variants are rare in early-onset and familial Parkinson's diseaseJarosław Dulski, Alexandra I Soto-Beasley, Ryan J Uitti, et al.
Irish Journal of Medical Science|March 22, 2021
PARKIN, PINK1, and DJ1 analysis in early-onset Parkinson's disease in IrelandDiana A Olszewska, Allan McCarthy, Alexandra I Soto-Beasley, et al.
Journal of Movement Disorders|April 30, 2021
Dancing Feet Dyskinesia in a Patient with GBA-PDDiana A Olszewska, Allan McCarthy, Alexandra I Soto-Beasley, et al.
Parkinsonism & Related Disorders|September 5, 2017
DCTN1 variation in pathologically-confirmed PSP and CBD tauopathyMonica Sanchez-Contreras, Alexandra I Soto, Ronald L Walton, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 13, 2009
Reported mutations in GIGYF2 are not a common cause of Parkinson's diseaseCarles Vilariño-Güell, Owen A Ross, Alexandra I Soto, et al.
Parkinsonism & Related Disorders|September 24, 2009
Histamine N-methyltransferase Thr105Ile is not associated with Parkinson's disease or essential tremorBrett H Keeling, Carles Vilariño-Güell, Alexandra I Soto-Ortolaza, et al.
Frontiers in Neurology|July 28, 2020
Association Between Glucocerebrosidase Mutations and Parkinson's Disease in IrelandDiana A Olszewska, Allan McCarthy, Alexandra I Soto-Beasley, et al.
Cells|August 12, 2022
Systematic Functional Analysis of <i>PINK1</i> and <i>PRKN</i> Coding VariantsBenjamin J Broadway, Paige K Boneski, Jenny M Bredenberg, et al.
Neurology|May 3, 2013
Similarities between familial and sporadic autopsy-proven progressive supranuclear palsyShinsuke Fujioka, Avi A Algom, Melissa E Murray, et al.
Pageof 11

Showing results (1-10 of 108) with videos related to

Sort By:
Pageof 11
Parkinsonism & Related Disorders|September 29, 2015
Genetic susceptibility variants in parkinsonismAlexandra I Soto-Ortolaza, Owen A Ross
Brain : a Journal of Neurology|July 14, 2023
PTPA variants are rare in early-onset and familial Parkinson's diseaseJarosław Dulski, Alexandra I Soto-Beasley, Ryan J Uitti, et al.
Irish Journal of Medical Science|March 22, 2021
PARKIN, PINK1, and DJ1 analysis in early-onset Parkinson's disease in IrelandDiana A Olszewska, Allan McCarthy, Alexandra I Soto-Beasley, et al.
Journal of Movement Disorders|April 30, 2021
Dancing Feet Dyskinesia in a Patient with GBA-PDDiana A Olszewska, Allan McCarthy, Alexandra I Soto-Beasley, et al.
Parkinsonism & Related Disorders|September 5, 2017
DCTN1 variation in pathologically-confirmed PSP and CBD tauopathyMonica Sanchez-Contreras, Alexandra I Soto, Ronald L Walton, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 13, 2009
Reported mutations in GIGYF2 are not a common cause of Parkinson's diseaseCarles Vilariño-Güell, Owen A Ross, Alexandra I Soto, et al.
Parkinsonism & Related Disorders|September 24, 2009
Histamine N-methyltransferase Thr105Ile is not associated with Parkinson's disease or essential tremorBrett H Keeling, Carles Vilariño-Güell, Alexandra I Soto-Ortolaza, et al.
Frontiers in Neurology|July 28, 2020
Association Between Glucocerebrosidase Mutations and Parkinson's Disease in IrelandDiana A Olszewska, Allan McCarthy, Alexandra I Soto-Beasley, et al.
Cells|August 12, 2022
Systematic Functional Analysis of <i>PINK1</i> and <i>PRKN</i> Coding VariantsBenjamin J Broadway, Paige K Boneski, Jenny M Bredenberg, et al.
Neurology|May 3, 2013
Similarities between familial and sporadic autopsy-proven progressive supranuclear palsyShinsuke Fujioka, Avi A Algom, Melissa E Murray, et al.
Pageof 11