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Lorenzo Cipriano

Showing results (1-10 of 26) with videos related to

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Therapeutic Advances in Neurological Disorders|January 15, 2026
Hereditary spastic paraplegia: from decades of therapy to future innovationsLorenzo Cipriano, Corrado Angelini, Filippo Maria Santorelli
Genes|October 29, 2025
Fluid Biomarkers in Hereditary Spastic Paraplegia: A Narrative Review and Integrative Framework for Complex Neurodegenerative MechanismsLorenzo Cipriano, Nunzio Setola, Melissa Barghigiani, et al.
Reviews in the Neurosciences|June 6, 2022
Is the pathology of posterior cortical atrophy clinically predictable?Lorenzo Cipriano, Mariano Oliva, Gianfranco Puoti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 22, 2023
MRI and steroid-responsive encephalopathy associated with autoimmune thyroiditis: first report of conus medullaris involvement and literature review of the known neuroimaging profilesLorenzo Cipriano, Giuseppina Miele, Lorenzo Ugga, et al.
Children (Basel, Switzerland)|May 25, 2024
Expanding the Phenotype of the CACNA1C-Associated Neurological Disorders in Children: Systematic Literature Review and Description of a Novel MutationLorenzo Cipriano, Raffaele Piscopo, Chiara Aiello, et al.
Genes|January 28, 2026
Interstitial 12p Deletion Syndrome: Revised Minimal Critical Region and Review of the LiteratureFlavia Privitera, Stefano Pagano, Lorenzo Cipriano, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 6, 2026
Neurodevelopmental disorders in childhood-onset hereditary spastic paraplegia type 7: a case series and review of literatureSara Satolli, Antonio Varone, Francesco Mari, et al.
Genes|September 28, 2024
A Novel De Novo <i>STAG1</i> Variant in Monozygotic Twins with Neurodevelopmental Disorder: New Insights in Clinical HeterogeneityLorenzo Cipriano, Roberta Russo, Immacolata Andolfo, et al.
Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association|April 4, 2021
Clinical and Genetic Heterogeneity in a Large Family with Pseudoxanthoma Elasticum: MTHFR and SERPINE1 Variants as Possible Disease Modifiers in Developing Ischemic StrokeGiorgia Bruno, Marco Ritelli, Andrea Di Pietro, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|January 23, 2023
Immunomodulatory effects of ocrelizumab and candidate biomarkers for monitoring treatment response in multiple sclerosisGianmarco Abbadessa, Giuseppina Miele, Elisabetta Maida, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
Therapeutic Advances in Neurological Disorders|January 15, 2026
Hereditary spastic paraplegia: from decades of therapy to future innovationsLorenzo Cipriano, Corrado Angelini, Filippo Maria Santorelli
Genes|October 29, 2025
Fluid Biomarkers in Hereditary Spastic Paraplegia: A Narrative Review and Integrative Framework for Complex Neurodegenerative MechanismsLorenzo Cipriano, Nunzio Setola, Melissa Barghigiani, et al.
Reviews in the Neurosciences|June 6, 2022
Is the pathology of posterior cortical atrophy clinically predictable?Lorenzo Cipriano, Mariano Oliva, Gianfranco Puoti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 22, 2023
MRI and steroid-responsive encephalopathy associated with autoimmune thyroiditis: first report of conus medullaris involvement and literature review of the known neuroimaging profilesLorenzo Cipriano, Giuseppina Miele, Lorenzo Ugga, et al.
Children (Basel, Switzerland)|May 25, 2024
Expanding the Phenotype of the CACNA1C-Associated Neurological Disorders in Children: Systematic Literature Review and Description of a Novel MutationLorenzo Cipriano, Raffaele Piscopo, Chiara Aiello, et al.
Genes|January 28, 2026
Interstitial 12p Deletion Syndrome: Revised Minimal Critical Region and Review of the LiteratureFlavia Privitera, Stefano Pagano, Lorenzo Cipriano, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 6, 2026
Neurodevelopmental disorders in childhood-onset hereditary spastic paraplegia type 7: a case series and review of literatureSara Satolli, Antonio Varone, Francesco Mari, et al.
Genes|September 28, 2024
A Novel De Novo <i>STAG1</i> Variant in Monozygotic Twins with Neurodevelopmental Disorder: New Insights in Clinical HeterogeneityLorenzo Cipriano, Roberta Russo, Immacolata Andolfo, et al.
Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association|April 4, 2021
Clinical and Genetic Heterogeneity in a Large Family with Pseudoxanthoma Elasticum: MTHFR and SERPINE1 Variants as Possible Disease Modifiers in Developing Ischemic StrokeGiorgia Bruno, Marco Ritelli, Andrea Di Pietro, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|January 23, 2023
Immunomodulatory effects of ocrelizumab and candidate biomarkers for monitoring treatment response in multiple sclerosisGianmarco Abbadessa, Giuseppina Miele, Elisabetta Maida, et al.
Pageof 3