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Lorenzo Maggi

Showing results (11-20 of 186) with videos related to

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Neuromuscular Disorders : NMD|May 26, 2023
253rd ENMC international workshop: Striated muscle laminopathies - natural history and clinical trial readiness. 24-26 June 2022, Hoofddorp, the NetherlandsLorenzo Maggi, Susana Quijano-Roy, Carsten Bönnemann, et al.
Cells|July 2, 2021
Ion Channel Gene Mutations Causing Skeletal Muscle Disorders: Pathomechanisms and Opportunities for TherapyLorenzo Maggi, Silvia Bonanno, Concetta Altamura, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|October 29, 2020
Salbutamol as effective treatment in slow-channel syndrome- first reportLuca Spiro Santovito, Raffaella Brugnoni, Paolo Banfi, et al.
Acta Neurologica Belgica|August 30, 2017
Reply to the letter by Finsterer et al. concerning the paper: "Affection of immune-cells by a C10orf2 mutation manifesting as mitochondrial myopathy and transient sensory transverse syndrome" by Galassi G. et alGiuliana Galassi, Lorenzo Maggi, Eleonora Lamantea, et al.
Acta Neurologica Belgica|May 22, 2017
C10ORF2 mutation associated with progressive external ophthalmoplegia and clinically isolated syndromeGiuliana Galassi, Lorenzo Maggi, Eleonora Lamantea, et al.
Journal of Robotic Surgery|June 19, 2026
Introduction of robotics into a well-established navigation OR team for TKA does not increase surgical time. A one center evaluationLorenzo Maggi, Yves Vanderschelden, David Burlot, et al.
International Journal of Molecular Sciences|April 30, 2021
Skeletal and Cardiac Muscle Disorders Caused by Mutations in Genes Encoding Intermediate Filament ProteinsLorenzo Maggi, Manolis Mavroidis, Stelios Psarras, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|March 16, 2021
Therapeutic efficacy of 3,4-Diaminopyridine phosphate on neuromuscular junction in Pompe diseaseCinzia Bragato, Flavia Blasevich, Gary Ingenito, et al.
Journal of Neuromuscular Diseases|April 3, 2023
Novel DPAGT1 Gene Mutation in Two Twins with Congenital Myasthenic Syndrome and a Review of the LiteratureMarta Cheli, Raffaella Brugnoni, Sara Gibertini, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 6, 2022
Sixth cranial nerve palsy after first intrathecal nusinersen administrationLuca Spiro Santovito, Silvia Bonanno, Luisa Chiapparini, et al.
Pageof 19

Showing results (11-20 of 186) with videos related to

Sort By:
Pageof 19
Neuromuscular Disorders : NMD|May 26, 2023
253rd ENMC international workshop: Striated muscle laminopathies - natural history and clinical trial readiness. 24-26 June 2022, Hoofddorp, the NetherlandsLorenzo Maggi, Susana Quijano-Roy, Carsten Bönnemann, et al.
Cells|July 2, 2021
Ion Channel Gene Mutations Causing Skeletal Muscle Disorders: Pathomechanisms and Opportunities for TherapyLorenzo Maggi, Silvia Bonanno, Concetta Altamura, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|October 29, 2020
Salbutamol as effective treatment in slow-channel syndrome- first reportLuca Spiro Santovito, Raffaella Brugnoni, Paolo Banfi, et al.
Acta Neurologica Belgica|August 30, 2017
Reply to the letter by Finsterer et al. concerning the paper: "Affection of immune-cells by a C10orf2 mutation manifesting as mitochondrial myopathy and transient sensory transverse syndrome" by Galassi G. et alGiuliana Galassi, Lorenzo Maggi, Eleonora Lamantea, et al.
Acta Neurologica Belgica|May 22, 2017
C10ORF2 mutation associated with progressive external ophthalmoplegia and clinically isolated syndromeGiuliana Galassi, Lorenzo Maggi, Eleonora Lamantea, et al.
Journal of Robotic Surgery|June 19, 2026
Introduction of robotics into a well-established navigation OR team for TKA does not increase surgical time. A one center evaluationLorenzo Maggi, Yves Vanderschelden, David Burlot, et al.
International Journal of Molecular Sciences|April 30, 2021
Skeletal and Cardiac Muscle Disorders Caused by Mutations in Genes Encoding Intermediate Filament ProteinsLorenzo Maggi, Manolis Mavroidis, Stelios Psarras, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|March 16, 2021
Therapeutic efficacy of 3,4-Diaminopyridine phosphate on neuromuscular junction in Pompe diseaseCinzia Bragato, Flavia Blasevich, Gary Ingenito, et al.
Journal of Neuromuscular Diseases|April 3, 2023
Novel DPAGT1 Gene Mutation in Two Twins with Congenital Myasthenic Syndrome and a Review of the LiteratureMarta Cheli, Raffaella Brugnoni, Sara Gibertini, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 6, 2022
Sixth cranial nerve palsy after first intrathecal nusinersen administrationLuca Spiro Santovito, Silvia Bonanno, Luisa Chiapparini, et al.
Pageof 19