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Maura Brunetti

Showing results (41-50 of 86) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|July 27, 2022
Systematic evaluation of genetic mutations in ALS: a population-based studyMaurizio Grassano, Andrea Calvo, Cristina Moglia, et al.
Annals of Neurology|April 3, 2024
High Frequency of Cognitive and Behavioral Impairment in Amyotrophic Lateral Sclerosis Patients with SOD1 Pathogenic VariantsAndrea Calvo, Cristina Moglia, Antonio Canosa, et al.
Neurology|January 23, 2024
Cognitive and Behavioral Features of Patients With Amyotrophic Lateral Sclerosis Who Are Carriers of the <i>TARDBP</i> Pathogenic VariantCristina Moglia, Andrea Calvo, Antonio Canosa, et al.
European Journal of Nuclear Medicine and Molecular Imaging|January 25, 2022
Amyotrophic lateral sclerosis with SOD1 mutations shows distinct brain metabolic changesAntonio Canosa, Andrea Calvo, Cristina Moglia, et al.
Neurology. Genetics|September 15, 2022
Phenotype Analysis of Fused in Sarcoma Mutations in Amyotrophic Lateral SclerosisMaurizio Grassano, Giorgia Brodini, Giovanni De Marco, et al.
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, Neurosurgery, and Psychiatry|September 29, 2021
GBA variants influence cognitive status in amyotrophic lateral sclerosisAntonio Canosa, Maurizio Grassano, Cristina Moglia, et al.
Neurology|August 15, 2019
Cognitive impairment across ALS clinical stages in a population-based cohortAdriano Chiò, Cristina Moglia, Antonio Canosa, 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.
Pageof 9

Showing results (41-50 of 86) with videos related to

Sort By:
Pageof 9
Journal of Neurology, Neurosurgery, and Psychiatry|July 27, 2022
Systematic evaluation of genetic mutations in ALS: a population-based studyMaurizio Grassano, Andrea Calvo, Cristina Moglia, et al.
Annals of Neurology|April 3, 2024
High Frequency of Cognitive and Behavioral Impairment in Amyotrophic Lateral Sclerosis Patients with SOD1 Pathogenic VariantsAndrea Calvo, Cristina Moglia, Antonio Canosa, et al.
Neurology|January 23, 2024
Cognitive and Behavioral Features of Patients With Amyotrophic Lateral Sclerosis Who Are Carriers of the <i>TARDBP</i> Pathogenic VariantCristina Moglia, Andrea Calvo, Antonio Canosa, et al.
European Journal of Nuclear Medicine and Molecular Imaging|January 25, 2022
Amyotrophic lateral sclerosis with SOD1 mutations shows distinct brain metabolic changesAntonio Canosa, Andrea Calvo, Cristina Moglia, et al.
Neurology. Genetics|September 15, 2022
Phenotype Analysis of Fused in Sarcoma Mutations in Amyotrophic Lateral SclerosisMaurizio Grassano, Giorgia Brodini, Giovanni De Marco, et al.
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, Neurosurgery, and Psychiatry|September 29, 2021
GBA variants influence cognitive status in amyotrophic lateral sclerosisAntonio Canosa, Maurizio Grassano, Cristina Moglia, et al.
Neurology|August 15, 2019
Cognitive impairment across ALS clinical stages in a population-based cohortAdriano Chiò, Cristina Moglia, Antonio Canosa, 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.
Pageof 9