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

Enza Maria Valente

Showing results (1-10 of 333) with videos related to

Pageof 34
Sort By:
Movement Disorders : Official Journal of the Movement Disorder Society|January 1, 2019
LRP10: A novel disease gene bridging Parkinson's disease and dementia with Lewy bodyFrancesca Morgante, Enza Maria Valente
The Lancet. Neurology|June 22, 2007
Heterozygous mutations in genes causing parkinsonism: monogenic disorders go complexEnza Maria Valente, Alessandro Ferraris
Movement Disorders Clinical Practice|May 7, 2020
Movement Disorders in Genetic Pediatric AtaxiasSimone Gana, Enza Maria Valente
Developmental Medicine and Child Neurology|February 22, 2024
Joubert syndrome and hydrocephalus: Further expanding the phenotypic spectrum of a pleiotropic ciliopathySimone Gana, Enza Maria Valente
Neurology|August 12, 2011
"Gluing" phenotypes together: the case of GLUT1Enza Maria Valente, Alberto Albanese
F1000 Biology Reports|October 16, 2010
Advances in the genetics of primary torsion dystoniaEnza Maria Valente, Alberto Albanese
Movement Disorders : Official Journal of the Movement Disorder Society|February 21, 2017
KMT2B: A new twist in dystonia geneticsBettina Balint, Enza Maria Valente
The Journal of Pathology|October 5, 2016
PINK1 in the limelight: multiple functions of an eclectic protein in human health and diseaseGiuseppe Arena, Enza Maria Valente
Frontiers in Neurology|April 19, 2013
Genetic issues in the diagnosis of dystoniasSimona Petrucci, Enza Maria Valente
Movement Disorders : Official Journal of the Movement Disorder Society|April 10, 2013
Novel genes and novel pathogenetic mechanisms in adult-onset primary dystoniaSimona Petrucci, Enza Maria Valente
Pageof 34

Showing results (1-10 of 333) with videos related to

Sort By:
Pageof 34
Movement Disorders : Official Journal of the Movement Disorder Society|January 1, 2019
LRP10: A novel disease gene bridging Parkinson's disease and dementia with Lewy bodyFrancesca Morgante, Enza Maria Valente
The Lancet. Neurology|June 22, 2007
Heterozygous mutations in genes causing parkinsonism: monogenic disorders go complexEnza Maria Valente, Alessandro Ferraris
Movement Disorders Clinical Practice|May 7, 2020
Movement Disorders in Genetic Pediatric AtaxiasSimone Gana, Enza Maria Valente
Developmental Medicine and Child Neurology|February 22, 2024
Joubert syndrome and hydrocephalus: Further expanding the phenotypic spectrum of a pleiotropic ciliopathySimone Gana, Enza Maria Valente
Neurology|August 12, 2011
"Gluing" phenotypes together: the case of GLUT1Enza Maria Valente, Alberto Albanese
F1000 Biology Reports|October 16, 2010
Advances in the genetics of primary torsion dystoniaEnza Maria Valente, Alberto Albanese
Movement Disorders : Official Journal of the Movement Disorder Society|February 21, 2017
KMT2B: A new twist in dystonia geneticsBettina Balint, Enza Maria Valente
The Journal of Pathology|October 5, 2016
PINK1 in the limelight: multiple functions of an eclectic protein in human health and diseaseGiuseppe Arena, Enza Maria Valente
Frontiers in Neurology|April 19, 2013
Genetic issues in the diagnosis of dystoniasSimona Petrucci, Enza Maria Valente
Movement Disorders : Official Journal of the Movement Disorder Society|April 10, 2013
Novel genes and novel pathogenetic mechanisms in adult-onset primary dystoniaSimona Petrucci, Enza Maria Valente
Pageof 34