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

Niccolo E Mencacci

Showing results (1-10 of 29) with videos related to

Pageof 3
Sort By:
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|September 17, 2019
Naming Genes for Dystonia: DYT-z or Ditzy?Niccolo E Mencacci, H A Jinnah
Neurology|July 9, 2016
Author ResponseNiccolo E Mencacci, Roberto Erro, Kailash P Bhatia
Movement Disorders : Official Journal of the Movement Disorder Society|November 15, 2023
Dystonia in ATP Synthase Defects: Reconnecting Mitochondria and DopamineElisabetta Indelicato, Sylvia Boesch, Niccolo' E Mencacci, et al.
Neurology|April 3, 2015
Cortical pencil lining in neuroferritinopathy: a diagnostic clueAmit Batla, Matthew E Adams, Roberto Erro, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 14, 2015
Web-based assessment of Parkinson's prodromal markers identifies GBA variantsAlastair J Noyce, Niccolo E Mencacci, Anette Schrag, et al.
Neurology|July 21, 2012
Myoclonus-dystonia syndrome due to tyrosine hydroxylase deficiencyMaria Stamelou, Niccolo E Mencacci, Carla Cordivari, et al.
Brain : a Journal of Neurology|November 16, 2014
Reply: Parkinson's disease in GTP cyclohydrolase 1 mutation carriersNiccolo E Mencacci, Alan M Pittman, Ioannis U Isaias, et al.
Neurobiology of Aging|December 14, 2020
Replication assessment of NUS1 variants in Parkinson's diseaseBernabe I Bustos, Sara Bandres-Ciga, J Raphael Gibbs, et al.
Movement Disorders Clinical Practice|October 27, 2018
Expanding the Phenotype and Genetic Defects Associated with the <i>GOSR2</i> GeneRoman Praschberger, Bettina Balint, Niccolo E Mencacci, et al.
Neurology|June 19, 2015
ADCY5 mutations are another cause of benign hereditary choreaNiccolo E Mencacci, Roberto Erro, Sarah Wiethoff, et al.
Pageof 3

Showing results (1-10 of 29) with videos related to

Sort By:
Pageof 3
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|September 17, 2019
Naming Genes for Dystonia: DYT-z or Ditzy?Niccolo E Mencacci, H A Jinnah
Neurology|July 9, 2016
Author ResponseNiccolo E Mencacci, Roberto Erro, Kailash P Bhatia
Movement Disorders : Official Journal of the Movement Disorder Society|November 15, 2023
Dystonia in ATP Synthase Defects: Reconnecting Mitochondria and DopamineElisabetta Indelicato, Sylvia Boesch, Niccolo' E Mencacci, et al.
Neurology|April 3, 2015
Cortical pencil lining in neuroferritinopathy: a diagnostic clueAmit Batla, Matthew E Adams, Roberto Erro, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 14, 2015
Web-based assessment of Parkinson's prodromal markers identifies GBA variantsAlastair J Noyce, Niccolo E Mencacci, Anette Schrag, et al.
Neurology|July 21, 2012
Myoclonus-dystonia syndrome due to tyrosine hydroxylase deficiencyMaria Stamelou, Niccolo E Mencacci, Carla Cordivari, et al.
Brain : a Journal of Neurology|November 16, 2014
Reply: Parkinson's disease in GTP cyclohydrolase 1 mutation carriersNiccolo E Mencacci, Alan M Pittman, Ioannis U Isaias, et al.
Neurobiology of Aging|December 14, 2020
Replication assessment of NUS1 variants in Parkinson's diseaseBernabe I Bustos, Sara Bandres-Ciga, J Raphael Gibbs, et al.
Movement Disorders Clinical Practice|October 27, 2018
Expanding the Phenotype and Genetic Defects Associated with the <i>GOSR2</i> GeneRoman Praschberger, Bettina Balint, Niccolo E Mencacci, et al.
Neurology|June 19, 2015
ADCY5 mutations are another cause of benign hereditary choreaNiccolo E Mencacci, Roberto Erro, Sarah Wiethoff, et al.
Pageof 3