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

Nilo Riva

Showing results (91-100 of 133) with videos related to

Pageof 14
Sort By:
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 7, 2019
ALS Cognitive Behavioral Screen (ALS-CBS): normative values for the Italian population and clinical usabilityLucio Tremolizzo, Andrea Lizio, Gabriella Santangelo, et al.
Journal of Neurology|June 29, 2023
Case report: coexistence of C9orf72 expansion and progranulin mutation in a case of genetic frontotemporal dementia-clinical features and neuroimaging correlatesAlma Ghirelli, Edoardo Gioele Spinelli, Elisa Canu, et al.
Journal of Neuroinflammation|November 15, 2025
Loss of C9orf72 impacts the peripheral neuromuscular system via immune dysregulation and accelerates the progression of amyotrophic lateral sclerosis in SOD-1 mutant miceFrancesca Sironi, Massimo Tortarolo, Sabrina Mazzucchi, et al.
Scientific Reports|December 17, 2016
Unraveling gene expression profiles in peripheral motor nerve from amyotrophic lateral sclerosis patients: insights into pathogenesisNilo Riva, Ferdinando Clarelli, Teuta Domi, et al.
International Journal of Molecular Sciences|May 14, 2020
Burden of Rare Variants in ALS and Axonal Hereditary Neuropathy Genes Influence Survival in ALS: Insights from a Next Generation Sequencing Study of an Italian ALS CohortStefania Scarlino, Teuta Domi, Laura Pozzi, et al.
Journal of Neurology|October 12, 2018
Functioning and quality of life in patients with neuropathy associated with anti-MAG antibodiesYuri M Falzone, Marta Campagnolo, Mariangela Bianco, et al.
Experimental Neurology|March 30, 2017
A longitudinal DTI and histological study of the spinal cord reveals early pathological alterations in G93A-SOD1 mouse model of amyotrophic lateral sclerosisStefania Marcuzzo, Silvia Bonanno, Matteo Figini, et al.
European Journal of Neurology|March 9, 2022
Integrated evaluation of a panel of neurochemical biomarkers to optimize diagnosis and prognosis in amyotrophic lateral sclerosisYuri Matteo Falzone, Teuta Domi, Alessandra Mandelli, et al.
Neurology|September 21, 2021
Structural MRI Signatures in Genetic Presentations of the Frontotemporal Dementia/Motor Neuron Disease SpectrumEdoardo Gioele Spinelli, Alma Ghirelli, Silvia Basaia, et al.
Frontiers in Oncology|October 13, 2022
Clinical and pathological findings in neurolymphomatosis: Preliminary association with gene expression profiles in sural nervesFederica Cerri, Francesco Gentile, Ferdinando Clarelli, et al.
Pageof 14

Showing results (91-100 of 133) with videos related to

Sort By:
Pageof 14
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 7, 2019
ALS Cognitive Behavioral Screen (ALS-CBS): normative values for the Italian population and clinical usabilityLucio Tremolizzo, Andrea Lizio, Gabriella Santangelo, et al.
Journal of Neurology|June 29, 2023
Case report: coexistence of C9orf72 expansion and progranulin mutation in a case of genetic frontotemporal dementia-clinical features and neuroimaging correlatesAlma Ghirelli, Edoardo Gioele Spinelli, Elisa Canu, et al.
Journal of Neuroinflammation|November 15, 2025
Loss of C9orf72 impacts the peripheral neuromuscular system via immune dysregulation and accelerates the progression of amyotrophic lateral sclerosis in SOD-1 mutant miceFrancesca Sironi, Massimo Tortarolo, Sabrina Mazzucchi, et al.
Scientific Reports|December 17, 2016
Unraveling gene expression profiles in peripheral motor nerve from amyotrophic lateral sclerosis patients: insights into pathogenesisNilo Riva, Ferdinando Clarelli, Teuta Domi, et al.
International Journal of Molecular Sciences|May 14, 2020
Burden of Rare Variants in ALS and Axonal Hereditary Neuropathy Genes Influence Survival in ALS: Insights from a Next Generation Sequencing Study of an Italian ALS CohortStefania Scarlino, Teuta Domi, Laura Pozzi, et al.
Journal of Neurology|October 12, 2018
Functioning and quality of life in patients with neuropathy associated with anti-MAG antibodiesYuri M Falzone, Marta Campagnolo, Mariangela Bianco, et al.
Experimental Neurology|March 30, 2017
A longitudinal DTI and histological study of the spinal cord reveals early pathological alterations in G93A-SOD1 mouse model of amyotrophic lateral sclerosisStefania Marcuzzo, Silvia Bonanno, Matteo Figini, et al.
European Journal of Neurology|March 9, 2022
Integrated evaluation of a panel of neurochemical biomarkers to optimize diagnosis and prognosis in amyotrophic lateral sclerosisYuri Matteo Falzone, Teuta Domi, Alessandra Mandelli, et al.
Neurology|September 21, 2021
Structural MRI Signatures in Genetic Presentations of the Frontotemporal Dementia/Motor Neuron Disease SpectrumEdoardo Gioele Spinelli, Alma Ghirelli, Silvia Basaia, et al.
Frontiers in Oncology|October 13, 2022
Clinical and pathological findings in neurolymphomatosis: Preliminary association with gene expression profiles in sural nervesFederica Cerri, Francesco Gentile, Ferdinando Clarelli, et al.
Pageof 14