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Maura Brunetti

Showing results (61-70 of 86) with videos related to

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Archives of Neurology|January 12, 2011
Large proportion of amyotrophic lateral sclerosis cases in Sardinia due to a single founder mutation of the TARDBP geneAdriano Chiò, Giuseppe Borghero, Maura Pugliatti, et al.
Annals of Neurology|February 20, 2025
Brain Metabolic Features of FUS-ALS: A 2-[<sup>18</sup>F]FDG-PET StudyAntonio Canosa, Umberto Manera, Rosario Vasta, et al.
Annals of Clinical and Translational Neurology|April 25, 2025
KIF5A p.Pro986Leu Risk Variant and Accelerated Progression of Amyotrophic Lateral SclerosisArianna Manini, Rosario Vasta, Alberto Brusati, et al.
Neurobiology of Aging|July 26, 2015
ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestryGiuseppe Borghero, Maura Pugliatti, Francesco Marrosu, et al.
Journal of Neurology|April 6, 2019
Parkinsonian traits in amyotrophic lateral sclerosis (ALS): a prospective population-based studyAndrea Calvo, Adriano Chiò, Marco Pagani, et al.
Journal of Neurology|August 22, 2025
Whole genome sequencing analysis in primary lateral sclerosis (PLS) patients reveals mutations in neurological diseases-causing genesArianna Manini, Alberto Brusati, Maurizio Grassano, et al.
Neurobiology of Aging|August 16, 2014
Genetic architecture of ALS in SardiniaGiuseppe Borghero, Maura Pugliatti, Francesco Marrosu, 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.
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.
Neurobiology of Aging|July 16, 2015
HFE p.H63D polymorphism does not influence ALS phenotype and survivalAdriano Chiò, Gabriele Mora, Mario Sabatelli, et al.
Pageof 9

Showing results (61-70 of 86) with videos related to

Sort By:
Pageof 9
Archives of Neurology|January 12, 2011
Large proportion of amyotrophic lateral sclerosis cases in Sardinia due to a single founder mutation of the TARDBP geneAdriano Chiò, Giuseppe Borghero, Maura Pugliatti, et al.
Annals of Neurology|February 20, 2025
Brain Metabolic Features of FUS-ALS: A 2-[<sup>18</sup>F]FDG-PET StudyAntonio Canosa, Umberto Manera, Rosario Vasta, et al.
Annals of Clinical and Translational Neurology|April 25, 2025
KIF5A p.Pro986Leu Risk Variant and Accelerated Progression of Amyotrophic Lateral SclerosisArianna Manini, Rosario Vasta, Alberto Brusati, et al.
Neurobiology of Aging|July 26, 2015
ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestryGiuseppe Borghero, Maura Pugliatti, Francesco Marrosu, et al.
Journal of Neurology|April 6, 2019
Parkinsonian traits in amyotrophic lateral sclerosis (ALS): a prospective population-based studyAndrea Calvo, Adriano Chiò, Marco Pagani, et al.
Journal of Neurology|August 22, 2025
Whole genome sequencing analysis in primary lateral sclerosis (PLS) patients reveals mutations in neurological diseases-causing genesArianna Manini, Alberto Brusati, Maurizio Grassano, et al.
Neurobiology of Aging|August 16, 2014
Genetic architecture of ALS in SardiniaGiuseppe Borghero, Maura Pugliatti, Francesco Marrosu, 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.
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.
Neurobiology of Aging|July 16, 2015
HFE p.H63D polymorphism does not influence ALS phenotype and survivalAdriano Chiò, Gabriele Mora, Mario Sabatelli, et al.
Pageof 9