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

S Cocozza

Showing results (61-70 of 81) with videos related to

Pageof 9
Sort By:
Annals of Neurology|March 1, 1995
Early-onset ataxia with cardiomyopathy and retained tendon reflexes maps to the Friedreich's ataxia locus on chromosome 9qF Palau, G De Michele, J J Vilchez, et al.
Journal of the Neurological Sciences|October 1, 1996
Autosomal dominant cerebellar ataxia type I. Clinical and molecular study in 36 Italian families including a comparison between SCA1 and SCA2 phenotypesA Filla, G De Michele, G Campanella, et al.
European Journal of Neurology|September 21, 2020
Diffuse brain connectivity changes in Charcot-Marie-Tooth type 1a patients: a resting-state functional magnetic resonance imaging studyG Pontillo, S Tozza, T Perillo, et al.
AJNR. American Journal of Neuroradiology|April 23, 2021
Unraveling Deep Gray Matter Atrophy and Iron and Myelin Changes in Multiple SclerosisG Pontillo, M Petracca, S Monti, et al.
European Journal of Neurology|November 2, 2016
Grey:white matter ratio at diagnosis and the risk of 10-year multiple sclerosis progressionM Moccia, M Quarantelli, R Lanzillo, et al.
Cell|July 11, 1998
Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloproteaseG Casari, M De Fusco, S Ciarmatori, et al.
Revista Do Hospital Das Clinicas|January 10, 2002
Friedreich's ataxia: clinical and molecular study of 25 Brazilian casesL M Albano, M Zatz, C A Kim, et al.
European Neurology|July 15, 2000
Relative frequencies of CAG expansions in spinocerebellar ataxia and dentatorubropallidoluysian atrophy in 116 Italian familiesA Filla, C Mariotti, G Caruso, et al.
Human Molecular Genetics|August 1, 1997
The Friedreich ataxia GAA triplet repeat: premutation and normal allelesL Montermini, E Andermann, M Labuda, et al.
Journal of Neurology|August 4, 1999
Spinocerebellar ataxia type 2 in southern Italy: a clinical and molecular study of 30 familiesA Filla, G De Michele, L Santoro, et al.
Pageof 9

Showing results (61-70 of 81) with videos related to

Sort By:
Pageof 9
Annals of Neurology|March 1, 1995
Early-onset ataxia with cardiomyopathy and retained tendon reflexes maps to the Friedreich's ataxia locus on chromosome 9qF Palau, G De Michele, J J Vilchez, et al.
Journal of the Neurological Sciences|October 1, 1996
Autosomal dominant cerebellar ataxia type I. Clinical and molecular study in 36 Italian families including a comparison between SCA1 and SCA2 phenotypesA Filla, G De Michele, G Campanella, et al.
European Journal of Neurology|September 21, 2020
Diffuse brain connectivity changes in Charcot-Marie-Tooth type 1a patients: a resting-state functional magnetic resonance imaging studyG Pontillo, S Tozza, T Perillo, et al.
AJNR. American Journal of Neuroradiology|April 23, 2021
Unraveling Deep Gray Matter Atrophy and Iron and Myelin Changes in Multiple SclerosisG Pontillo, M Petracca, S Monti, et al.
European Journal of Neurology|November 2, 2016
Grey:white matter ratio at diagnosis and the risk of 10-year multiple sclerosis progressionM Moccia, M Quarantelli, R Lanzillo, et al.
Cell|July 11, 1998
Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloproteaseG Casari, M De Fusco, S Ciarmatori, et al.
Revista Do Hospital Das Clinicas|January 10, 2002
Friedreich's ataxia: clinical and molecular study of 25 Brazilian casesL M Albano, M Zatz, C A Kim, et al.
European Neurology|July 15, 2000
Relative frequencies of CAG expansions in spinocerebellar ataxia and dentatorubropallidoluysian atrophy in 116 Italian familiesA Filla, C Mariotti, G Caruso, et al.
Human Molecular Genetics|August 1, 1997
The Friedreich ataxia GAA triplet repeat: premutation and normal allelesL Montermini, E Andermann, M Labuda, et al.
Journal of Neurology|August 4, 1999
Spinocerebellar ataxia type 2 in southern Italy: a clinical and molecular study of 30 familiesA Filla, G De Michele, L Santoro, et al.
Pageof 9