Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Antonio Toscano

Showing results (101-110 of 223) with videos related to

Pageof 23
Sort By:
Cerebrovascular Diseases (Basel, Switzerland)|February 6, 2020
Isolated Insular Stroke: Clinical PresentationFabrizio Giammello, Domenico Cosenza, Carmela Casella, et al.
Annals of Neurology|September 5, 2002
Mutations of mitochondrial DNA polymerase gammaA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegiaEleonora Lamantea, Valeria Tiranti, Andreina Bordoni, et al.
Frontiers in Genetics|June 17, 2022
Case Report: Rare Homozygous <i>RNASEH1</i> Mutations Associated With Adult-Onset Mitochondrial Encephalomyopathy and Multiple Mitochondrial DNA DeletionsArianna Manini, Leonardo Caporali, Megi Meneri, et al.
Neuromuscular Disorders : NMD|August 2, 2015
Homozygosity for the common GAA gene splice site mutation c.-32-13T>G in Pompe disease is associated with the classical adult phenotypical spectrumOlimpia Musumeci, Andrea Thieme, Kristl G Claeys, et al.
Journal of Inherited Metabolic Disease|September 17, 2010
Changes in skeletal muscle qualities during enzyme replacement therapy in late-onset type II glycogenosis: temporal and spatial pattern of mass vs. strength responseSabrina Ravaglia, Anna Pichiecchio, Michela Ponzio, et al.
Autophagy|August 8, 2018
ZFYVE26/SPASTIZIN and SPG11/SPATACSIN mutations in hereditary spastic paraplegia types AR-SPG15 and AR-SPG11 have different effects on autophagy and endocytosisChiara Vantaggiato, Elena Panzeri, Marianna Castelli, et al.
Acta Neurologica Belgica|March 8, 2023
Paraneoplastic neurological syndromes of the central nervous system: a single institution 7-year case seriesFabrizio Giammello, Karol Galletta, Francesco Grillo, et al.
Neuromuscular Disorders : NMD|February 12, 2009
Immune-mediated rippling muscle disease with myasthenia gravis: a report of seven patients with long-term follow-up in twoBenedikt Schoser, Saiju Jacob, David Hilton-Jones, et al.
Journal of Muscle Research and Cell Motility|March 30, 2006
Immunohistochemical analysis of human skeletal muscle AMP deaminase deficiency. Evidence of a correlation between the muscle HPRG content and the level of the residual AMP deaminase activityAntonietta R M Sabbatini, Antonio Toscano, Mohammed Aguennouz, et al.
World Neurosurgery|June 1, 2024
Predictors of Good Functional Outcome in Patients with Tandem Occlusion After Revascularization Treatment: Single-Center Experience with 12-Month Follow-UpLudovica Ferraù, Fabrizio Giammello, Agostino Tessitore, et al.
Pageof 23

Showing results (101-110 of 223) with videos related to

Sort By:
Pageof 23
Cerebrovascular Diseases (Basel, Switzerland)|February 6, 2020
Isolated Insular Stroke: Clinical PresentationFabrizio Giammello, Domenico Cosenza, Carmela Casella, et al.
Annals of Neurology|September 5, 2002
Mutations of mitochondrial DNA polymerase gammaA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegiaEleonora Lamantea, Valeria Tiranti, Andreina Bordoni, et al.
Frontiers in Genetics|June 17, 2022
Case Report: Rare Homozygous <i>RNASEH1</i> Mutations Associated With Adult-Onset Mitochondrial Encephalomyopathy and Multiple Mitochondrial DNA DeletionsArianna Manini, Leonardo Caporali, Megi Meneri, et al.
Neuromuscular Disorders : NMD|August 2, 2015
Homozygosity for the common GAA gene splice site mutation c.-32-13T>G in Pompe disease is associated with the classical adult phenotypical spectrumOlimpia Musumeci, Andrea Thieme, Kristl G Claeys, et al.
Journal of Inherited Metabolic Disease|September 17, 2010
Changes in skeletal muscle qualities during enzyme replacement therapy in late-onset type II glycogenosis: temporal and spatial pattern of mass vs. strength responseSabrina Ravaglia, Anna Pichiecchio, Michela Ponzio, et al.
Autophagy|August 8, 2018
ZFYVE26/SPASTIZIN and SPG11/SPATACSIN mutations in hereditary spastic paraplegia types AR-SPG15 and AR-SPG11 have different effects on autophagy and endocytosisChiara Vantaggiato, Elena Panzeri, Marianna Castelli, et al.
Acta Neurologica Belgica|March 8, 2023
Paraneoplastic neurological syndromes of the central nervous system: a single institution 7-year case seriesFabrizio Giammello, Karol Galletta, Francesco Grillo, et al.
Neuromuscular Disorders : NMD|February 12, 2009
Immune-mediated rippling muscle disease with myasthenia gravis: a report of seven patients with long-term follow-up in twoBenedikt Schoser, Saiju Jacob, David Hilton-Jones, et al.
Journal of Muscle Research and Cell Motility|March 30, 2006
Immunohistochemical analysis of human skeletal muscle AMP deaminase deficiency. Evidence of a correlation between the muscle HPRG content and the level of the residual AMP deaminase activityAntonietta R M Sabbatini, Antonio Toscano, Mohammed Aguennouz, et al.
World Neurosurgery|June 1, 2024
Predictors of Good Functional Outcome in Patients with Tandem Occlusion After Revascularization Treatment: Single-Center Experience with 12-Month Follow-UpLudovica Ferraù, Fabrizio Giammello, Agostino Tessitore, et al.
Pageof 23