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

C Lamperti

Showing results (11-20 of 23) with videos related to

Pageof 3
Sort By:
Neurology|April 26, 2001
Lack of apoptosis in mitochondrial encephalomyopathiesM Sciacco, G Fagiolari, C Lamperti, et al.
Neurology|December 10, 2003
A CAV3 microdeletion differentially affects skeletal muscle and myocardiumR Cagliani, N Bresolin, A Prelle, et al.
Journal of Inherited Metabolic Disease|April 10, 2009
Neuropathological study of skeletal muscle, heart, liver, and brain in a neonatal form of glycogen storage disease type IV associated with a new mutation in GBE1 geneC Lamperti, S Salani, S Lucchiari, et al.
Neurology|April 12, 2003
Cerebellar ataxia and coenzyme Q10 deficiencyC Lamperti, A Naini, M Hirano, et al.
Neurology|October 24, 2008
Mutated mitofusin 2 presents with intrafamilial variability and brain mitochondrial dysfunctionR Del Bo, M Moggio, M Rango, et al.
Neurology|June 27, 2002
Clinicopathological features of genetically confirmed Danon diseaseK Sugie, A Yamamoto, K Murayama, et al.
Journal of the Neurological Sciences|October 13, 2010
New molecular findings in congenital myopathies due to selenoprotein N gene mutationsR Cagliani, M E Fruguglietti, A Berardinelli, et al.
Journal of Neurology|July 14, 2021
Adult-onset mitochondrial movement disorders: a national picture from the Italian NetworkV Montano, D Orsucci, V Carelli, et al.
Journal of Neurology|October 13, 2001
Retrospective study of a large population of patients affected with mitochondrial disorders: clinical, morphological and molecular genetic evaluationM Sciacco, A Prelle, G P Comi, et al.
Journal of Neurology|August 18, 2022
Primary mitochondrial myopathy: 12-month follow-up results of an Italian cohortV Montano, P Lopriore, F Gruosso, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Neurology|April 26, 2001
Lack of apoptosis in mitochondrial encephalomyopathiesM Sciacco, G Fagiolari, C Lamperti, et al.
Neurology|December 10, 2003
A CAV3 microdeletion differentially affects skeletal muscle and myocardiumR Cagliani, N Bresolin, A Prelle, et al.
Journal of Inherited Metabolic Disease|April 10, 2009
Neuropathological study of skeletal muscle, heart, liver, and brain in a neonatal form of glycogen storage disease type IV associated with a new mutation in GBE1 geneC Lamperti, S Salani, S Lucchiari, et al.
Neurology|April 12, 2003
Cerebellar ataxia and coenzyme Q10 deficiencyC Lamperti, A Naini, M Hirano, et al.
Neurology|October 24, 2008
Mutated mitofusin 2 presents with intrafamilial variability and brain mitochondrial dysfunctionR Del Bo, M Moggio, M Rango, et al.
Neurology|June 27, 2002
Clinicopathological features of genetically confirmed Danon diseaseK Sugie, A Yamamoto, K Murayama, et al.
Journal of the Neurological Sciences|October 13, 2010
New molecular findings in congenital myopathies due to selenoprotein N gene mutationsR Cagliani, M E Fruguglietti, A Berardinelli, et al.
Journal of Neurology|July 14, 2021
Adult-onset mitochondrial movement disorders: a national picture from the Italian NetworkV Montano, D Orsucci, V Carelli, et al.
Journal of Neurology|October 13, 2001
Retrospective study of a large population of patients affected with mitochondrial disorders: clinical, morphological and molecular genetic evaluationM Sciacco, A Prelle, G P Comi, et al.
Journal of Neurology|August 18, 2022
Primary mitochondrial myopathy: 12-month follow-up results of an Italian cohortV Montano, P Lopriore, F Gruosso, et al.
Pageof 3