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

Maura Brunetti

Showing results (71-80 of 86) with videos related to

Pageof 9
Sort By:
Neurobiology of Aging|March 2, 2015
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patientsAdriano Chiò, Gabriele Mora, Mario Sabatelli, et al.
Biomedicines|March 29, 2023
The <i>HFE</i> p.H63D (p.His63Asp) Polymorphism Is a Modifier of ALS Outcome in Italian and French Patients with <i>SOD1</i> MutationsAntonio Canosa, Andrea Calvo, Gabriele Mora, et al.
Neurobiology of Aging|January 7, 2016
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansionAdriano Chiò, Gabriele Mora, Mario Sabatelli, et al.
Neurobiology of Aging|December 15, 2022
Whole genome sequencing analysis reveals post-zygotic mutation variability in monozygotic twins discordant for amyotrophic lateral sclerosisGijs H P Tazelaar, Paul J Hop, Meinie Seelen, et al.
Brain : a Journal of Neurology|April 22, 2026
Machine learning model based on plasma proteomics for the identification of Parkinson's diseaseBoluwatife Adewale, Ruth Chia, Ruin Moaddel, et al.
Neuron|December 15, 2010
Exome sequencing reveals VCP mutations as a cause of familial ALSJanel O Johnson, Jessica Mandrioli, Michael Benatar, et al.
Nature Medicine|August 19, 2025
A plasma proteomics-based candidate biomarker panel predictive of amyotrophic lateral sclerosisRuth Chia, Ruin Moaddel, Justin Y Kwan, et al.
Brain : a Journal of Neurology|February 28, 2012
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72Adriano Chiò, Giuseppe Borghero, Gabriella Restagno, et al.
Neurobiology of Aging|March 16, 2012
C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS populationMario Sabatelli, Francesca Luisa Conforti, Marcella Zollino, et al.
Science Translational Medicine|February 23, 2022
Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALSPaul J Hop, Ramona A J Zwamborn, Eilis Hannon, et al.
Pageof 9

Showing results (71-80 of 86) with videos related to

Sort By:
Pageof 9
Neurobiology of Aging|March 2, 2015
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patientsAdriano Chiò, Gabriele Mora, Mario Sabatelli, et al.
Biomedicines|March 29, 2023
The <i>HFE</i> p.H63D (p.His63Asp) Polymorphism Is a Modifier of ALS Outcome in Italian and French Patients with <i>SOD1</i> MutationsAntonio Canosa, Andrea Calvo, Gabriele Mora, et al.
Neurobiology of Aging|January 7, 2016
ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansionAdriano Chiò, Gabriele Mora, Mario Sabatelli, et al.
Neurobiology of Aging|December 15, 2022
Whole genome sequencing analysis reveals post-zygotic mutation variability in monozygotic twins discordant for amyotrophic lateral sclerosisGijs H P Tazelaar, Paul J Hop, Meinie Seelen, et al.
Brain : a Journal of Neurology|April 22, 2026
Machine learning model based on plasma proteomics for the identification of Parkinson's diseaseBoluwatife Adewale, Ruth Chia, Ruin Moaddel, et al.
Neuron|December 15, 2010
Exome sequencing reveals VCP mutations as a cause of familial ALSJanel O Johnson, Jessica Mandrioli, Michael Benatar, et al.
Nature Medicine|August 19, 2025
A plasma proteomics-based candidate biomarker panel predictive of amyotrophic lateral sclerosisRuth Chia, Ruin Moaddel, Justin Y Kwan, et al.
Brain : a Journal of Neurology|February 28, 2012
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72Adriano Chiò, Giuseppe Borghero, Gabriella Restagno, et al.
Neurobiology of Aging|March 16, 2012
C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS populationMario Sabatelli, Francesca Luisa Conforti, Marcella Zollino, et al.
Science Translational Medicine|February 23, 2022
Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALSPaul J Hop, Ramona A J Zwamborn, Eilis Hannon, et al.
Pageof 9