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

Diana Rodriguez

Showing results (141-150 of 193) with videos related to

Pageof 20
Sort By:
Brain : a Journal of Neurology|May 26, 2011
Mutations of TSEN and CASK genes are prevalent in pontocerebellar hypoplasias type 2 and 4Vassili Valayannopoulos, Caroline Michot, Diana Rodriguez, et al.
Neurology. Genetics|November 2, 2020
Congenital immobility and stiffness related to biallelic <i>ATAD1</i> variantsRoxane Bunod, Diane Doummar, Sandra Whalen, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 20, 2016
Clinical, radiological and possible pathological overlap of cystic leukoencephalopathy without megalencephaly and Aicardi-Goutières syndromeDavide Tonduti, Simona Orcesi, Emma M Jenkinson, et al.
Orphanet Journal of Rare Diseases|March 29, 2012
Spectrum of pontocerebellar hypoplasia in 13 girls and boys with CASK mutations: confirmation of a recognizable phenotype and first description of a male mosaic patientLydie Burglen, Sandra Chantot-Bastaraud, Catherine Garel, et al.
Molecular Genetics and Metabolism|February 5, 2015
Case definition and classification of leukodystrophies and leukoencephalopathiesAdeline Vanderver, Morgan Prust, Davide Tonduti, et al.
Genes|August 25, 2019
One <i>NF1</i> Mutation may Conceal AnotherLaurence Pacot, Cyril Burin des Roziers, Ingrid Laurendeau, et al.
Contemporary Clinical Trials|August 14, 2020
The Aging<sup>PLUS</sup> trial: Design of a randomized controlled trial to increase physical activity in middle-aged and older adultsManfred Diehl, Abigail Nehrkorn-Bailey, Katherine Thompson, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 21, 2025
Neurological outcomes and disability predictors in paediatric herpes simplex virus encephalitis: a multicentre cohort from French tertiary hospitalsCaroline Rey, Laetitia Giorgi, Hélène Maurey, et al.
Journal of Clinical Medicine|June 26, 2026
Frailty and Congestion in Patients with Heart Failure: Clinical Interaction and Prognostic ImplicationsÁngela Rodríguez-Eguren, Joan Llevadot-Sesmilo, José Jesús Broseta, et al.
Lancet (London, England)|July 29, 2008
Prevalence of dementia in Latin America, India, and China: a population-based cross-sectional surveyJuan J Llibre Rodriguez, Cleusa P Ferri, Daisy Acosta, et al.
Pageof 20

Showing results (141-150 of 193) with videos related to

Sort By:
Pageof 20
Brain : a Journal of Neurology|May 26, 2011
Mutations of TSEN and CASK genes are prevalent in pontocerebellar hypoplasias type 2 and 4Vassili Valayannopoulos, Caroline Michot, Diana Rodriguez, et al.
Neurology. Genetics|November 2, 2020
Congenital immobility and stiffness related to biallelic <i>ATAD1</i> variantsRoxane Bunod, Diane Doummar, Sandra Whalen, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 20, 2016
Clinical, radiological and possible pathological overlap of cystic leukoencephalopathy without megalencephaly and Aicardi-Goutières syndromeDavide Tonduti, Simona Orcesi, Emma M Jenkinson, et al.
Orphanet Journal of Rare Diseases|March 29, 2012
Spectrum of pontocerebellar hypoplasia in 13 girls and boys with CASK mutations: confirmation of a recognizable phenotype and first description of a male mosaic patientLydie Burglen, Sandra Chantot-Bastaraud, Catherine Garel, et al.
Molecular Genetics and Metabolism|February 5, 2015
Case definition and classification of leukodystrophies and leukoencephalopathiesAdeline Vanderver, Morgan Prust, Davide Tonduti, et al.
Genes|August 25, 2019
One <i>NF1</i> Mutation may Conceal AnotherLaurence Pacot, Cyril Burin des Roziers, Ingrid Laurendeau, et al.
Contemporary Clinical Trials|August 14, 2020
The Aging<sup>PLUS</sup> trial: Design of a randomized controlled trial to increase physical activity in middle-aged and older adultsManfred Diehl, Abigail Nehrkorn-Bailey, Katherine Thompson, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 21, 2025
Neurological outcomes and disability predictors in paediatric herpes simplex virus encephalitis: a multicentre cohort from French tertiary hospitalsCaroline Rey, Laetitia Giorgi, Hélène Maurey, et al.
Journal of Clinical Medicine|June 26, 2026
Frailty and Congestion in Patients with Heart Failure: Clinical Interaction and Prognostic ImplicationsÁngela Rodríguez-Eguren, Joan Llevadot-Sesmilo, José Jesús Broseta, et al.
Lancet (London, England)|July 29, 2008
Prevalence of dementia in Latin America, India, and China: a population-based cross-sectional surveyJuan J Llibre Rodriguez, Cleusa P Ferri, Daisy Acosta, et al.
Pageof 20