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

Barbara Garavaglia

Showing results (91-100 of 129) with videos related to

Pageof 13
Sort By:
Movement Disorders : Official Journal of the Movement Disorder Society|April 20, 2006
Frequency and phenotypes of LRRK2 G2019S mutation in Italian patients with Parkinson's diseaseRoberta Marongiu, Daniele Ghezzi, Tamara Ialongo, et al.
Brain : a Journal of Neurology|March 2, 2023
Variants in ATP5F1B are associated with dominantly inherited dystoniaAlessia Nasca, Niccolò E Mencacci, Federica Invernizzi, et al.
Journal of Neuropathology and Experimental Neurology|January 26, 2025
α-Synuclein distribution in olfactory mucosa and skin nerves in Parkinson disease associated with an EIF4G1 gene mutationArianna Braccia, Antonio Emanuele Elia, Grazia Devigili, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 20, 2016
Clinical, radiological and possible pathological overlap of cystic leukoencephalopathy without megalencephaly and Aicardi-Goutières syndromeDavide Tonduti, Simona Orcesi, Emma M Jenkinson, et al.
International Journal of Molecular Sciences|July 12, 2025
LC-MS/MS-Based Determination of Ambroxol in Human Plasma and Cerebrospinal Fluid: Validation and Applicability in a Phase II Study on GBA-Associated Parkinson's Disease PatientsValentina Franco, Michela Palmisani, Fabiana Colucci, et al.
Movement Disorders Clinical Practice|January 31, 2024
Dominant VPS16 Pathogenic Variants: Not Only Isolated DystoniaEdoardo Monfrini, Laura Avanzino, Giovanni Palermo, et al.
Biochemical and Biophysical Research Communications|January 13, 2009
Variant late infantile ceroid lipofuscinoses associated with novel mutations in CLN6Natalia Cannelli, Barbara Garavaglia, Alessandro Simonati, et al.
Parkinsonism & Related Disorders|June 4, 2008
Parkin analysis in early onset Parkinson's diseaseFrancesca Sironi, Paola Primignani, Michela Zini, et al.
Brain Communications|December 9, 2022
Adult-onset KMT2B-related dystoniaEdoardo Monfrini, Andrea Ciolfi, Francesco Cavallieri, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 20, 2019
Frequency and phenotypic spectrum of KMT2B dystonia in childhood: A single-center cohort studyMiryam Carecchio, Federica Invernizzi, Paulina Gonzàlez-Latapi, et al.
Pageof 13

Showing results (91-100 of 129) with videos related to

Sort By:
Pageof 13
Movement Disorders : Official Journal of the Movement Disorder Society|April 20, 2006
Frequency and phenotypes of LRRK2 G2019S mutation in Italian patients with Parkinson's diseaseRoberta Marongiu, Daniele Ghezzi, Tamara Ialongo, et al.
Brain : a Journal of Neurology|March 2, 2023
Variants in ATP5F1B are associated with dominantly inherited dystoniaAlessia Nasca, Niccolò E Mencacci, Federica Invernizzi, et al.
Journal of Neuropathology and Experimental Neurology|January 26, 2025
α-Synuclein distribution in olfactory mucosa and skin nerves in Parkinson disease associated with an EIF4G1 gene mutationArianna Braccia, Antonio Emanuele Elia, Grazia Devigili, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 20, 2016
Clinical, radiological and possible pathological overlap of cystic leukoencephalopathy without megalencephaly and Aicardi-Goutières syndromeDavide Tonduti, Simona Orcesi, Emma M Jenkinson, et al.
International Journal of Molecular Sciences|July 12, 2025
LC-MS/MS-Based Determination of Ambroxol in Human Plasma and Cerebrospinal Fluid: Validation and Applicability in a Phase II Study on GBA-Associated Parkinson's Disease PatientsValentina Franco, Michela Palmisani, Fabiana Colucci, et al.
Movement Disorders Clinical Practice|January 31, 2024
Dominant VPS16 Pathogenic Variants: Not Only Isolated DystoniaEdoardo Monfrini, Laura Avanzino, Giovanni Palermo, et al.
Biochemical and Biophysical Research Communications|January 13, 2009
Variant late infantile ceroid lipofuscinoses associated with novel mutations in CLN6Natalia Cannelli, Barbara Garavaglia, Alessandro Simonati, et al.
Parkinsonism & Related Disorders|June 4, 2008
Parkin analysis in early onset Parkinson's diseaseFrancesca Sironi, Paola Primignani, Michela Zini, et al.
Brain Communications|December 9, 2022
Adult-onset KMT2B-related dystoniaEdoardo Monfrini, Andrea Ciolfi, Francesco Cavallieri, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 20, 2019
Frequency and phenotypic spectrum of KMT2B dystonia in childhood: A single-center cohort studyMiryam Carecchio, Federica Invernizzi, Paulina Gonzàlez-Latapi, et al.
Pageof 13