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Neurology and Therapy|June 20, 2026
ECAS-Based Neuropsychological Phenotyping in Amyotrophic Lateral Sclerosis: A Retrospective Study Comparing Different AlgorithmsBarbara Poletti, Edoardo N Aiello, Monica Consonni, et al.
European Journal of Neurology|November 7, 2025
Cognitive Reserve in Amyotrophic Lateral Sclerosis: A 2-[18F]FDG-PET Study on Sex-Related DifferencesAntonio Canosa, Stefano Callegaro, Umberto Manera, et al.
Neurobiology of Aging|May 9, 2016
TBK1 is associated with ALS and ALS-FTD in Sardinian patientsGiuseppe Borghero, Maura Pugliatti, Francesco Marrosu, et al.
Neurobiology of Aging|February 9, 2010
FUS mutations in sporadic amyotrophic lateral sclerosisShiao-Lin Lai, Yevgeniya Abramzon, Jennifer C Schymick, et al.
Scientific Reports|April 13, 2019
Exome array analysis of rare and low frequency variants in amyotrophic lateral sclerosisAnnelot M Dekker, Frank P Diekstra, Sara L Pulit, et al.
Brain Communications|October 28, 2021
SCFD1 expression quantitative trait loci in amyotrophic lateral sclerosis are differentially expressedAlfredo Iacoangeli, Isabella Fogh, Sashika Selvackadunco, 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.
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|March 2, 2015
CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patientsAdriano Chiò, Gabriele Mora, Mario Sabatelli, et al.
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