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Laura Pozzi

Showing results (21-30 of 36) with videos related to

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Neurology|March 17, 2023
Clinical Features and Biomarkers to Differentiate Primary and Amyotrophic Lateral Sclerosis in Patients With an Upper Motor Neuron SyndromeParide Schito, Tommaso Russo, Teuta Domi, et al.
Frontiers in Neurology|August 1, 2022
Profiling morphologic MRI features of motor neuron disease caused by <i>TARDBP</i> mutationsEdoardo Gioele Spinelli, Alma Ghirelli, Nilo Riva, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|April 23, 2019
Concurrence of NMOSD and ALS in a patient with hexanucleotide repeat expansions of C9orf72Yuri Matteo Falzone, Marta Radaelli, Federica Agosta, et al.
Frontiers in Neuroscience|June 29, 2023
A novel <i>GRN</i> mutation in an Italian patient with non-fluent variant of primary progressive aphasia at onset: a longitudinal case reportVeronica Castelnovo, Elisa Canu, Teuta Domi, et al.
European Journal of Neurology|June 23, 2026
Tolerability, Safety and Effectiveness of Sigh Introduction During Non-Invasive Mechanical Ventilation Cycles in Patients With Amyotrophic Lateral SclerosisNilo Riva, Paride Schito, Tommaso Russo, et al.
Journal of Neurology|May 27, 2024
Update on recent advances in amyotrophic lateral sclerosisNilo Riva, Teuta Domi, Laura Pozzi, et al.
Journal of Neurology|April 20, 2020
Serum phosphorylated neurofilament heavy-chain levels reflect phenotypic heterogeneity and are an independent predictor of survival in motor neuron diseaseYuri Matteo Falzone, Teuta Domi, Federica Agosta, et al.
The Journal of Biological Chemistry|October 29, 2011
c-Jun N-terminal kinase regulates soluble Aβ oligomers and cognitive impairment in AD mouse modelAlessandra Sclip, Xanthi Antoniou, Alessio Colombo, et al.
Neurobiology of Aging|April 20, 2019
Coexistence of variants in TBK1 and in other ALS-related genes elucidates an oligogenic model of pathogenesis in sporadic ALSSerena Lattante, Paolo Niccolò Doronzio, Giuseppe Marangi, et al.
Journal of Neurology|June 29, 2023
Case report: coexistence of C9orf72 expansion and progranulin mutation in a case of genetic frontotemporal dementia-clinical features and neuroimaging correlatesAlma Ghirelli, Edoardo Gioele Spinelli, Elisa Canu, et al.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
Neurology|March 17, 2023
Clinical Features and Biomarkers to Differentiate Primary and Amyotrophic Lateral Sclerosis in Patients With an Upper Motor Neuron SyndromeParide Schito, Tommaso Russo, Teuta Domi, et al.
Frontiers in Neurology|August 1, 2022
Profiling morphologic MRI features of motor neuron disease caused by <i>TARDBP</i> mutationsEdoardo Gioele Spinelli, Alma Ghirelli, Nilo Riva, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|April 23, 2019
Concurrence of NMOSD and ALS in a patient with hexanucleotide repeat expansions of C9orf72Yuri Matteo Falzone, Marta Radaelli, Federica Agosta, et al.
Frontiers in Neuroscience|June 29, 2023
A novel <i>GRN</i> mutation in an Italian patient with non-fluent variant of primary progressive aphasia at onset: a longitudinal case reportVeronica Castelnovo, Elisa Canu, Teuta Domi, et al.
European Journal of Neurology|June 23, 2026
Tolerability, Safety and Effectiveness of Sigh Introduction During Non-Invasive Mechanical Ventilation Cycles in Patients With Amyotrophic Lateral SclerosisNilo Riva, Paride Schito, Tommaso Russo, et al.
Journal of Neurology|May 27, 2024
Update on recent advances in amyotrophic lateral sclerosisNilo Riva, Teuta Domi, Laura Pozzi, et al.
Journal of Neurology|April 20, 2020
Serum phosphorylated neurofilament heavy-chain levels reflect phenotypic heterogeneity and are an independent predictor of survival in motor neuron diseaseYuri Matteo Falzone, Teuta Domi, Federica Agosta, et al.
The Journal of Biological Chemistry|October 29, 2011
c-Jun N-terminal kinase regulates soluble Aβ oligomers and cognitive impairment in AD mouse modelAlessandra Sclip, Xanthi Antoniou, Alessio Colombo, et al.
Neurobiology of Aging|April 20, 2019
Coexistence of variants in TBK1 and in other ALS-related genes elucidates an oligogenic model of pathogenesis in sporadic ALSSerena Lattante, Paolo Niccolò Doronzio, Giuseppe Marangi, et al.
Journal of Neurology|June 29, 2023
Case report: coexistence of C9orf72 expansion and progranulin mutation in a case of genetic frontotemporal dementia-clinical features and neuroimaging correlatesAlma Ghirelli, Edoardo Gioele Spinelli, Elisa Canu, et al.
Pageof 4