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Daniela Bernardo

Showing results (11-20 of 17) with videos related to

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Human Molecular Genetics|January 14, 2021
Novel variants and cellular studies on patients' primary fibroblasts support a role for NEK1 missense variants in ALS pathogenesisSerena Lattante, Paolo Niccolò Doronzio, Amelia Conte, et al.
Genes|January 8, 2025
Exploring the Role of <i>CCNF</i> Variants in Italian ALS PatientsGiulia Bisogni, Amelia Conte, Umberto Costantino, et al.
Journal of Neurology|June 11, 2025
Burden of pathogenetic and likely pathogenetic variants in SPG7, SPG11 and AP4 genes in Amyotrophic Lateral Sclerosis. A case-control studyPaolo Niccolò Doronzio, Serena Lattante, Daniela Bernardo, 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 Cachexia, Sarcopenia and Muscle|January 19, 2026
Muscle Imaging in Inclusion Body Myositis: Refinement of MRI Criteria and Insights Into Upper Body InvolvementEleonora Torchia, Matteo Lucchini, José Verdu-Diaz, et al.
European Journal of Neurology|February 3, 2023
Evaluating the contribution of the gene TARDBP in Italian patients with amyotrophic lateral sclerosisSerena Lattante, Mario Sabatelli, Giulia Bisogni, et al.
Journal of Neurology|June 3, 2024
Long-term treatment of SOD1 ALS with tofersen: a multicentre experience in 17 patientsMario Sabatelli, Federica Cerri, Riccardo Zuccarino, et al.
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Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Human Molecular Genetics|January 14, 2021
Novel variants and cellular studies on patients' primary fibroblasts support a role for NEK1 missense variants in ALS pathogenesisSerena Lattante, Paolo Niccolò Doronzio, Amelia Conte, et al.
Genes|January 8, 2025
Exploring the Role of <i>CCNF</i> Variants in Italian ALS PatientsGiulia Bisogni, Amelia Conte, Umberto Costantino, et al.
Journal of Neurology|June 11, 2025
Burden of pathogenetic and likely pathogenetic variants in SPG7, SPG11 and AP4 genes in Amyotrophic Lateral Sclerosis. A case-control studyPaolo Niccolò Doronzio, Serena Lattante, Daniela Bernardo, 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 Cachexia, Sarcopenia and Muscle|January 19, 2026
Muscle Imaging in Inclusion Body Myositis: Refinement of MRI Criteria and Insights Into Upper Body InvolvementEleonora Torchia, Matteo Lucchini, José Verdu-Diaz, et al.
European Journal of Neurology|February 3, 2023
Evaluating the contribution of the gene TARDBP in Italian patients with amyotrophic lateral sclerosisSerena Lattante, Mario Sabatelli, Giulia Bisogni, et al.
Journal of Neurology|June 3, 2024
Long-term treatment of SOD1 ALS with tofersen: a multicentre experience in 17 patientsMario Sabatelli, Federica Cerri, Riccardo Zuccarino, et al.
Pageof 2