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Gabriele Mora

Showing results (91-100 of 117) with videos related to

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Neurology|October 6, 2017
Meta-analysis of pharmacogenetic interactions in amyotrophic lateral sclerosis clinical trialsRuben P A van Eijk, Ashley R Jones, William Sproviero, et al.
Neurobiology of Aging|February 9, 2010
FUS mutations in sporadic amyotrophic lateral sclerosisShiao-Lin Lai, Yevgeniya Abramzon, Jennifer C Schymick, et al.
Brain : a Journal of Neurology|April 27, 2021
The unfolded protein response in amyotrophic later sclerosis: results of a phase 2 trialEleonora Dalla Bella, Enrica Bersano, Giovanni Antonini, et al.
Journal of Neurology|September 16, 2017
Comorbidity of dementia with amyotrophic lateral sclerosis (ALS): insights from a large multicenter Italian cohortFrancesca Trojsi, Mattia Siciliano, Cinzia Femiano, et al.
Neurobiology of Aging|July 16, 2015
HFE p.H63D polymorphism does not influence ALS phenotype and survivalAdriano Chiò, Gabriele Mora, Mario Sabatelli, et al.
Frontiers in Neuroscience|June 4, 2019
Comparative Analysis of <i>C9orf72</i> and Sporadic Disease in a Large Multicenter ALS Population: The Effect of Male Sex on Survival of <i>C9orf72</i> Positive PatientsFrancesca Trojsi, Mattia Siciliano, Cinzia Femiano, et al.
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.
The Lancet. Neurology|October 11, 2014
Analysis of amyotrophic lateral sclerosis as a multistep process: a population-based modelling studyAmmar Al-Chalabi, Andrea Calvo, Adriano Chio, 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|September 20, 2011
Chromosome 9 ALS and FTD locus is probably derived from a single founderKin Mok, Bryan J Traynor, Jennifer Schymick, et al.
Pageof 12

Showing results (91-100 of 117) with videos related to

Sort By:
Pageof 12
Neurology|October 6, 2017
Meta-analysis of pharmacogenetic interactions in amyotrophic lateral sclerosis clinical trialsRuben P A van Eijk, Ashley R Jones, William Sproviero, et al.
Neurobiology of Aging|February 9, 2010
FUS mutations in sporadic amyotrophic lateral sclerosisShiao-Lin Lai, Yevgeniya Abramzon, Jennifer C Schymick, et al.
Brain : a Journal of Neurology|April 27, 2021
The unfolded protein response in amyotrophic later sclerosis: results of a phase 2 trialEleonora Dalla Bella, Enrica Bersano, Giovanni Antonini, et al.
Journal of Neurology|September 16, 2017
Comorbidity of dementia with amyotrophic lateral sclerosis (ALS): insights from a large multicenter Italian cohortFrancesca Trojsi, Mattia Siciliano, Cinzia Femiano, et al.
Neurobiology of Aging|July 16, 2015
HFE p.H63D polymorphism does not influence ALS phenotype and survivalAdriano Chiò, Gabriele Mora, Mario Sabatelli, et al.
Frontiers in Neuroscience|June 4, 2019
Comparative Analysis of <i>C9orf72</i> and Sporadic Disease in a Large Multicenter ALS Population: The Effect of Male Sex on Survival of <i>C9orf72</i> Positive PatientsFrancesca Trojsi, Mattia Siciliano, Cinzia Femiano, et al.
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.
The Lancet. Neurology|October 11, 2014
Analysis of amyotrophic lateral sclerosis as a multistep process: a population-based modelling studyAmmar Al-Chalabi, Andrea Calvo, Adriano Chio, 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|September 20, 2011
Chromosome 9 ALS and FTD locus is probably derived from a single founderKin Mok, Bryan J Traynor, Jennifer Schymick, et al.
Pageof 12