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

Luca Marsili

Showing results (111-120 of 120) with videos related to

Pageof 12
Sort By:
You have reached the last page of results.This site can display upto 120 results.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 21, 2020
The odyssey of complex neurogenetic disorders: From undetermined to positiveValeria Salinas, Patricia Vega, Luca Marsili, et al.
Neurology. Clinical Practice|June 30, 2025
Community Disadvantage Is Associated With More Severe Motor Symptoms in Parkinson DiseaseEmily J Hill, Samuel Blaise Marcucci, Kelly DeLano, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 9, 2020
Appropriateness, safety, and effectiveness of "drip and ship" teleconsultation model in Southeastern Tuscany: a feasibility studySimone Gallerini, Luca Marsili, Vincenzo Groccia, et al.
Research Square|October 7, 2024
The <i>LRRK2</i> p.L1795F variant causes Parkinson's disease in the European populationLara M Lange, Kristin Levine, Susan H Fox, et al.
NPJ Parkinson'S Disease|March 26, 2025
The LRRK2 p.L1795F variant causes Parkinson's disease in the European populationLara M Lange, Kristin Levine, Susan H Fox, et al.
Frontiers in Aging Neuroscience|November 2, 2020
Phenotype-Agnostic Molecular Subtyping of Neurodegenerative Disorders: The Cincinnati Cohort Biomarker Program (CCBP)Andrea Sturchio, Luca Marsili, Joaquin A Vizcarra, et al.
Archives of Neurology|February 16, 2011
Excessive daytime sleepiness in multiple system atrophy (SLEEMSA study)Claudia Moreno-López, Joan Santamaría, Manuel Salamero, et al.
Neurology|February 13, 2019
Revisiting protein aggregation as pathogenic in sporadic Parkinson and Alzheimer diseasesAlberto J Espay, Joaquin A Vizcarra, Luca Marsili, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 23, 2019
The Parkinson's disease e-diary: Developing a clinical and research tool for the digital ageJoaquin A Vizcarra, Álvaro Sánchez-Ferro, Walter Maetzler, et al.
American Journal of Human Genetics|June 10, 2023
Extreme phenotypic heterogeneity in non-expansion spinocerebellar ataxiasPaulina Cunha, Emilien Petit, Marie Coutelier, et al.
Pageof 12

Showing results (111-120 of 120) with videos related to

Sort By:
Pageof 12
You have reached the last page of results.This site can display upto 120 results.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 21, 2020
The odyssey of complex neurogenetic disorders: From undetermined to positiveValeria Salinas, Patricia Vega, Luca Marsili, et al.
Neurology. Clinical Practice|June 30, 2025
Community Disadvantage Is Associated With More Severe Motor Symptoms in Parkinson DiseaseEmily J Hill, Samuel Blaise Marcucci, Kelly DeLano, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 9, 2020
Appropriateness, safety, and effectiveness of "drip and ship" teleconsultation model in Southeastern Tuscany: a feasibility studySimone Gallerini, Luca Marsili, Vincenzo Groccia, et al.
Research Square|October 7, 2024
The <i>LRRK2</i> p.L1795F variant causes Parkinson's disease in the European populationLara M Lange, Kristin Levine, Susan H Fox, et al.
NPJ Parkinson'S Disease|March 26, 2025
The LRRK2 p.L1795F variant causes Parkinson's disease in the European populationLara M Lange, Kristin Levine, Susan H Fox, et al.
Frontiers in Aging Neuroscience|November 2, 2020
Phenotype-Agnostic Molecular Subtyping of Neurodegenerative Disorders: The Cincinnati Cohort Biomarker Program (CCBP)Andrea Sturchio, Luca Marsili, Joaquin A Vizcarra, et al.
Archives of Neurology|February 16, 2011
Excessive daytime sleepiness in multiple system atrophy (SLEEMSA study)Claudia Moreno-López, Joan Santamaría, Manuel Salamero, et al.
Neurology|February 13, 2019
Revisiting protein aggregation as pathogenic in sporadic Parkinson and Alzheimer diseasesAlberto J Espay, Joaquin A Vizcarra, Luca Marsili, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 23, 2019
The Parkinson's disease e-diary: Developing a clinical and research tool for the digital ageJoaquin A Vizcarra, Álvaro Sánchez-Ferro, Walter Maetzler, et al.
American Journal of Human Genetics|June 10, 2023
Extreme phenotypic heterogeneity in non-expansion spinocerebellar ataxiasPaulina Cunha, Emilien Petit, Marie Coutelier, et al.
Pageof 12