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

Javier Ruiz

Showing results (611-620 of 645) with videos related to

Pageof 65
Sort By:
Movement Disorders : Official Journal of the Movement Disorder Society|July 27, 2019
Cancer outcomes among Parkinson's disease patients with leucine rich repeat kinase 2 mutations, idiopathic Parkinson's disease patients, and nonaffected controlsIlir Agalliu, Roberto A Ortega, Marta San Luciano, et al.
NPJ Parkinson'S Disease|January 9, 2024
A potential patient stratification biomarker for Parkinson´s disease based on LRRK2 kinase-mediated centrosomal alterations in peripheral blood-derived cellsYahaira Naaldijk, Belén Fernández, Rachel Fasiczka, et al.
European Journal of Neurology|July 6, 2026
Neuropsychiatric Adverse Events Associated With Foslevodopa/Foscarbidopa Continuous Subcutaneous Infusion in Clinical Practice: A Multicenter StudyDavid Campo-Caballero, Jon Rodriguez-Antiguedad, Arnau Puig-Davi, et al.
European Journal of Neurology|August 14, 2023
Frequency and phenotypic spectrum of spinocerebellar ataxia 27B and other genetic ataxias in a Spanish cohort of late-onset cerebellar ataxiaPablo Iruzubieta, David Pellerin, Alberto Bergareche, et al.
Neuron|November 16, 2004
Cloning of the gene containing mutations that cause PARK8-linked Parkinson's diseaseCoro Paisán-Ruíz, Shushant Jain, E Whitney Evans, et al.
Molecular Neurodegeneration|January 24, 2018
Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylationJesús Madero-Pérez, Elena Fdez, Belén Fernández, et al.
Medrxiv : the Preprint Server for Health Sciences|July 3, 2026
Large-scale functional annotation establishes a reference framework for human <i>LRRK2</i> variantsAnthea Cheung, Neringa Pratuseviciute, Kirsten Black, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 23, 2017
Penetrance estimate of LRRK2 p.G2019S mutation in individuals of non-Ashkenazi Jewish ancestryAnnie J Lee, Yuanjia Wang, Roy N Alcalay, et al.
Acta Neuropathologica|June 14, 2021
R1441G but not G2019S mutation enhances LRRK2 mediated Rab10 phosphorylation in human peripheral blood neutrophilsYing Fan, Raja S Nirujogi, Alicia Garrido, et al.
Plos Medicine|June 4, 2014
Efficacy of pneumococcal nontypable Haemophilus influenzae protein D conjugate vaccine (PHiD-CV) in young Latin American children: A double-blind randomized controlled trialMiguel W Tregnaghi, Xavier Sáez-Llorens, Pio López, et al.
Pageof 65

Showing results (611-620 of 645) with videos related to

Sort By:
Pageof 65
Movement Disorders : Official Journal of the Movement Disorder Society|July 27, 2019
Cancer outcomes among Parkinson's disease patients with leucine rich repeat kinase 2 mutations, idiopathic Parkinson's disease patients, and nonaffected controlsIlir Agalliu, Roberto A Ortega, Marta San Luciano, et al.
NPJ Parkinson'S Disease|January 9, 2024
A potential patient stratification biomarker for Parkinson´s disease based on LRRK2 kinase-mediated centrosomal alterations in peripheral blood-derived cellsYahaira Naaldijk, Belén Fernández, Rachel Fasiczka, et al.
European Journal of Neurology|July 6, 2026
Neuropsychiatric Adverse Events Associated With Foslevodopa/Foscarbidopa Continuous Subcutaneous Infusion in Clinical Practice: A Multicenter StudyDavid Campo-Caballero, Jon Rodriguez-Antiguedad, Arnau Puig-Davi, et al.
European Journal of Neurology|August 14, 2023
Frequency and phenotypic spectrum of spinocerebellar ataxia 27B and other genetic ataxias in a Spanish cohort of late-onset cerebellar ataxiaPablo Iruzubieta, David Pellerin, Alberto Bergareche, et al.
Neuron|November 16, 2004
Cloning of the gene containing mutations that cause PARK8-linked Parkinson's diseaseCoro Paisán-Ruíz, Shushant Jain, E Whitney Evans, et al.
Molecular Neurodegeneration|January 24, 2018
Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylationJesús Madero-Pérez, Elena Fdez, Belén Fernández, et al.
Medrxiv : the Preprint Server for Health Sciences|July 3, 2026
Large-scale functional annotation establishes a reference framework for human <i>LRRK2</i> variantsAnthea Cheung, Neringa Pratuseviciute, Kirsten Black, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 23, 2017
Penetrance estimate of LRRK2 p.G2019S mutation in individuals of non-Ashkenazi Jewish ancestryAnnie J Lee, Yuanjia Wang, Roy N Alcalay, et al.
Acta Neuropathologica|June 14, 2021
R1441G but not G2019S mutation enhances LRRK2 mediated Rab10 phosphorylation in human peripheral blood neutrophilsYing Fan, Raja S Nirujogi, Alicia Garrido, et al.
Plos Medicine|June 4, 2014
Efficacy of pneumococcal nontypable Haemophilus influenzae protein D conjugate vaccine (PHiD-CV) in young Latin American children: A double-blind randomized controlled trialMiguel W Tregnaghi, Xavier Sáez-Llorens, Pio López, et al.
Pageof 65