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Neurobiology of Aging|August 2, 2011
A patient carrying a homozygous p.A382T TARDBP missense mutation shows a syndrome including ALS, extrapyramidal symptoms, and FTDGiuseppe Borghero, Gianluca Floris, Antonino Cannas, et al.Journal of Neurology|July 21, 2025
Exploring the phenotypic fingerprints of ANXA11 variants in ALS: a population-based study in an European cohortFrancesca Palumbo, Barbara Iazzolino, Cristina Moglia, et al.Neurology|December 21, 2014
ATXN2 polyQ intermediate repeats are a modifier of ALS survivalAdriano Chiò, Andrea Calvo, Cristina Moglia, et al.Neurology|November 19, 2020
Mutational Analysis of Known ALS Genes in an Italian Population-Based CohortMaurizio Grassano, Andrea Calvo, Cristina Moglia, et al.Journal of Neurology|October 24, 2022
Factors predicting disease progression in C9ORF72 ALS patientsJessica Mandrioli, Elisabetta Zucchi, Ilaria Martinelli, et al.Neurology|January 8, 2020
ALS phenotype is influenced by age, sex, and genetics: A population-based studyAdriano Chiò, Cristina Moglia, Antonio Canosa, et al.Journal of Neurology, Neurosurgery, and Psychiatry|August 25, 2022
Exploring the phenotype of Italian patients with ALS with intermediate ATXN2 polyQ repeatsAdriano Chio, Cristina Moglia, Antonio Canosa, et al.Journal of Neurology, Neurosurgery, and Psychiatry|May 3, 2012
ALS/FTD phenotype in two Sardinian families carrying both C9ORF72 and TARDBP mutationsAdriano Chiò, Gabriella Restagno, Maura Brunetti, et al.Journal of Neurology|September 5, 2023
Predictors for progression in amyotrophic lateral sclerosis associated to SOD1 mutation: insight from two population-based registriesIlaria Martinelli, Andrea Ghezzi, Elisabetta Zucchi, et al.Neurology. Genetics|October 31, 2022
Clinical and Metabolic Signature of UNC13A rs12608932 Variant in Amyotrophic Lateral SclerosisAndrea Calvo, Antonio Canosa, Cristina Moglia, et al.Pageof 8