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

Giulia Coarelli

Showing results (21-30 of 72) with videos related to

Pageof 8
Sort By:
European Journal of Neurology|January 6, 2025
Substantia nigra degeneration in spinocerebellar ataxia 2 and 7 using neuromelanin-sensitive imagingLydia Chougar, Giulia Coarelli, François-Xavier Lejeune, et al.
Clinical Neurology and Neurosurgery|July 5, 2018
Corrigendum to "Novel homozygous GBA2 mutation in a patient with complicated spastic paraplegia" [Clin. Neurol. Neurosurg. 168 (May) (2018) 60-63]Giulia Coarelli, Silvia Romano, Lorena Travaglini, et al.
Clinical Neurology and Neurosurgery|March 11, 2018
Novel homozygous GBA2 mutation in a patient with complicated spastic paraplegiaGiulia Coarelli, Silvia Romano, Lorena Travaglini, et al.
Psycho-Oncology|April 7, 2018
Assessing cognitive function in patients treated with immune checkpoint inhibitors: A feasibility studyStefania Cuzzubbo, Catherine Belin, Kader Chouahnia, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 28, 2024
Digital Gait Measures Capture 1-Year Progression in Early-Stage Spinocerebellar Ataxia Type 2Jens Seemann, Lina Daghsen, Matthieu Cazier, et al.
Neurology. Clinical Practice|October 19, 2023
End-of-Life Discussions With Patients and Caregivers Affected By Neurogenetic DiseasesAnne-Claire Dorsemans, Giulia Coarelli, Anna Heinzmann, et al.
Journal of Medical Genetics|October 21, 2022
Reproductive choices and intrafamilial communication in neurogenetic diseases with different self-estimated severitiesLucie Pierron, Sophie Tezenas du Montcel, Anna Heinzmann, et al.
European Journal of Neurology|December 20, 2024
Hereditary spastic paraplegias: When to expect bladder dysfunction a genetic and urodynamic studyPauline Lallemant-Dudek, Marine Guillaud-Bataille, Claire Hentzen, et al.
Plos One|May 23, 2013
A "candidate-interactome" aggregate analysis of genome-wide association data in multiple sclerosisRosella Mechelli, Renato Umeton, Claudia Policano, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|August 21, 2013
Screening for neurotropic viruses in cerebrospinal fluid of patients with multiple sclerosis and other neurological diseasesRosella Mechelli, Danila Vittori, Giulia Coarelli, et al.
Pageof 8

Showing results (21-30 of 72) with videos related to

Sort By:
Pageof 8
European Journal of Neurology|January 6, 2025
Substantia nigra degeneration in spinocerebellar ataxia 2 and 7 using neuromelanin-sensitive imagingLydia Chougar, Giulia Coarelli, François-Xavier Lejeune, et al.
Clinical Neurology and Neurosurgery|July 5, 2018
Corrigendum to "Novel homozygous GBA2 mutation in a patient with complicated spastic paraplegia" [Clin. Neurol. Neurosurg. 168 (May) (2018) 60-63]Giulia Coarelli, Silvia Romano, Lorena Travaglini, et al.
Clinical Neurology and Neurosurgery|March 11, 2018
Novel homozygous GBA2 mutation in a patient with complicated spastic paraplegiaGiulia Coarelli, Silvia Romano, Lorena Travaglini, et al.
Psycho-Oncology|April 7, 2018
Assessing cognitive function in patients treated with immune checkpoint inhibitors: A feasibility studyStefania Cuzzubbo, Catherine Belin, Kader Chouahnia, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 28, 2024
Digital Gait Measures Capture 1-Year Progression in Early-Stage Spinocerebellar Ataxia Type 2Jens Seemann, Lina Daghsen, Matthieu Cazier, et al.
Neurology. Clinical Practice|October 19, 2023
End-of-Life Discussions With Patients and Caregivers Affected By Neurogenetic DiseasesAnne-Claire Dorsemans, Giulia Coarelli, Anna Heinzmann, et al.
Journal of Medical Genetics|October 21, 2022
Reproductive choices and intrafamilial communication in neurogenetic diseases with different self-estimated severitiesLucie Pierron, Sophie Tezenas du Montcel, Anna Heinzmann, et al.
European Journal of Neurology|December 20, 2024
Hereditary spastic paraplegias: When to expect bladder dysfunction a genetic and urodynamic studyPauline Lallemant-Dudek, Marine Guillaud-Bataille, Claire Hentzen, et al.
Plos One|May 23, 2013
A "candidate-interactome" aggregate analysis of genome-wide association data in multiple sclerosisRosella Mechelli, Renato Umeton, Claudia Policano, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|August 21, 2013
Screening for neurotropic viruses in cerebrospinal fluid of patients with multiple sclerosis and other neurological diseasesRosella Mechelli, Danila Vittori, Giulia Coarelli, et al.
Pageof 8