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

Franco Taroni

Showing results (81-90 of 204) with videos related to

Pageof 21
Sort By:
Cerebellum (London, England)|August 23, 2024
Phenotypic Spectrum and Natural History of Gillespie Syndrome. An Updated Literature Review with 2 New CasesClaudia Ciaccio, Matilde Taddei, Chiara Pantaleoni, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|April 1, 2020
Severe worsening of adult-onset Alexander disease after minor head trauma: Report of two patients and review of the literatureChiara Benzoni, Domenico Aquino, Daniela Di Bella, et al.
Journal of the Peripheral Nervous System : JPNS|August 27, 2015
Mutational mechanisms in MFN2-related neuropathy: compound heterozygosity for recessive and semidominant mutationsGiuseppe Piscosquito, Paola Saveri, Stefania Magri, et al.
BMJ Case Reports|June 21, 2011
A novel founder mutation in the MFN2 gene associated with variable Charcot-Marie-Tooth type 2 phenotype in two families from Southern ItalyMaria Muglia, Giovanni Vazza, Alessandra Patitucci, et al.
Neuromuscular Disorders : NMD|June 9, 2009
Novel mutations in the GDAP1 gene in patients affected with early-onset axonal Charcot-Marie-Tooth type 4AIsabella Moroni, Michela Morbin, Micaela Milani, et al.
Cerebellum (London, England)|September 5, 2008
Spinocerebellar ataxia type 28: a novel autosomal dominant cerebellar ataxia characterized by slow progression and ophthalmoparesisCaterina Mariotti, Alfredo Brusco, Daniela Di Bella, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 18, 2007
Rapid progression of late onset axonal Charcot-Marie-Tooth disease associated with a novel MPZ mutation in the extracellular domainMatilde Laurà, Micaela Milani, Michela Morbin, et al.
Journal of Child Neurology|June 1, 2005
Electroencephalographic recordings of focal seizures in patients affected by periventricular nodular heterotopia: role of the heterotopic nodules in the genesis of epileptic dischargesGiorgio Battaglia, Silvana Franceschetti, Luisa Chiapparini, et al.
Journal of the Peripheral Nervous System : JPNS|May 28, 2014
X-linked Charcot-Marie-Tooth type 1: stroke-like presentation of a novel GJB1 mutationAnna Sagnelli, Giuseppe Piscosquito, Luisa Chiapparini, et al.
Science & Justice : Journal of the Forensic Science Society|October 6, 2016
Discussion on how to implement a verbal scale in a forensic laboratory: Benefits, pitfalls and suggestions to avoid misunderstandingsRaymond Marquis, Alex Biedermann, Liv Cadola, et al.
Pageof 21

Showing results (81-90 of 204) with videos related to

Sort By:
Pageof 21
Cerebellum (London, England)|August 23, 2024
Phenotypic Spectrum and Natural History of Gillespie Syndrome. An Updated Literature Review with 2 New CasesClaudia Ciaccio, Matilde Taddei, Chiara Pantaleoni, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|April 1, 2020
Severe worsening of adult-onset Alexander disease after minor head trauma: Report of two patients and review of the literatureChiara Benzoni, Domenico Aquino, Daniela Di Bella, et al.
Journal of the Peripheral Nervous System : JPNS|August 27, 2015
Mutational mechanisms in MFN2-related neuropathy: compound heterozygosity for recessive and semidominant mutationsGiuseppe Piscosquito, Paola Saveri, Stefania Magri, et al.
BMJ Case Reports|June 21, 2011
A novel founder mutation in the MFN2 gene associated with variable Charcot-Marie-Tooth type 2 phenotype in two families from Southern ItalyMaria Muglia, Giovanni Vazza, Alessandra Patitucci, et al.
Neuromuscular Disorders : NMD|June 9, 2009
Novel mutations in the GDAP1 gene in patients affected with early-onset axonal Charcot-Marie-Tooth type 4AIsabella Moroni, Michela Morbin, Micaela Milani, et al.
Cerebellum (London, England)|September 5, 2008
Spinocerebellar ataxia type 28: a novel autosomal dominant cerebellar ataxia characterized by slow progression and ophthalmoparesisCaterina Mariotti, Alfredo Brusco, Daniela Di Bella, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 18, 2007
Rapid progression of late onset axonal Charcot-Marie-Tooth disease associated with a novel MPZ mutation in the extracellular domainMatilde Laurà, Micaela Milani, Michela Morbin, et al.
Journal of Child Neurology|June 1, 2005
Electroencephalographic recordings of focal seizures in patients affected by periventricular nodular heterotopia: role of the heterotopic nodules in the genesis of epileptic dischargesGiorgio Battaglia, Silvana Franceschetti, Luisa Chiapparini, et al.
Journal of the Peripheral Nervous System : JPNS|May 28, 2014
X-linked Charcot-Marie-Tooth type 1: stroke-like presentation of a novel GJB1 mutationAnna Sagnelli, Giuseppe Piscosquito, Luisa Chiapparini, et al.
Science & Justice : Journal of the Forensic Science Society|October 6, 2016
Discussion on how to implement a verbal scale in a forensic laboratory: Benefits, pitfalls and suggestions to avoid misunderstandingsRaymond Marquis, Alex Biedermann, Liv Cadola, et al.
Pageof 21