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

P Rebelo

Showing results (41-50 of 64) with videos related to

Pageof 7
Sort By:
Biorxiv : the Preprint Server for Biology|December 18, 2023
Sord deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insightsAdriana P Rebelo, Clemer Abad, Maike F Dohrn, et al.
Neurology|May 5, 2017
Novel mutations in <i>dystonin</i> provide clues to the pathomechanisms of HSAN-VIFiore Manganelli, Silvia Parisi, Maria Nolano, et al.
Brain : a Journal of Neurology|March 27, 2024
SORD-deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insightsAdriana P Rebelo, Clemer Abad, Maike F Dohrn, et al.
Neurology|February 3, 2022
De Novo <i>ATP1A1</i> Variants in an Early-Onset Complex Neurodevelopmental SyndromeMaike F Dohrn, Adriana P Rebelo, Siddharth Srivastava, et al.
ACS Infectious Diseases|September 4, 2019
Flexible 3D Cell-Based Platforms for the Discovery and Profiling of Novel Drugs Targeting <i>Plasmodium</i> Hepatic InfectionFrancisca Arez, Sofia P Rebelo, Diana Fontinha, et al.
Brain Communications|December 11, 2023
Novel variant in <i>CADM3</i> causes Charcot-Marie-Tooth diseaseAbdoulaye Yalcouyé, Adriana P Rebelo, Lassana Cissé, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 22, 2022
BiP inactivation due to loss of the deAMPylation function of FICD causes a motor neuron diseaseAdriana P Rebelo, Ariel Ruiz, Maike F Dohrn, et al.
Brain : a Journal of Neurology|April 23, 2021
A CADM3 variant causes Charcot-Marie-Tooth disease with marked upper limb involvementAdriana P Rebelo, Andrea Cortese, Amit Abraham, et al.
Neurology. Genetics|May 24, 2019
Autosomal dominant optic atrophy and cataract "plus" phenotype including axonal neuropathyAlejandro Horga, Enrico Bugiardini, Andreea Manole, et al.
Brain : a Journal of Neurology|May 26, 2021
Erratum to: A CADM3 variant causes Charcot-Marie-Tooth disease with marked upper limb involvementAdriana P Rebelo, Andrea Cortese, Amit Abraham, et al.
Pageof 7

Showing results (41-50 of 64) with videos related to

Sort By:
Pageof 7
Biorxiv : the Preprint Server for Biology|December 18, 2023
Sord deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insightsAdriana P Rebelo, Clemer Abad, Maike F Dohrn, et al.
Neurology|May 5, 2017
Novel mutations in <i>dystonin</i> provide clues to the pathomechanisms of HSAN-VIFiore Manganelli, Silvia Parisi, Maria Nolano, et al.
Brain : a Journal of Neurology|March 27, 2024
SORD-deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insightsAdriana P Rebelo, Clemer Abad, Maike F Dohrn, et al.
Neurology|February 3, 2022
De Novo <i>ATP1A1</i> Variants in an Early-Onset Complex Neurodevelopmental SyndromeMaike F Dohrn, Adriana P Rebelo, Siddharth Srivastava, et al.
ACS Infectious Diseases|September 4, 2019
Flexible 3D Cell-Based Platforms for the Discovery and Profiling of Novel Drugs Targeting <i>Plasmodium</i> Hepatic InfectionFrancisca Arez, Sofia P Rebelo, Diana Fontinha, et al.
Brain Communications|December 11, 2023
Novel variant in <i>CADM3</i> causes Charcot-Marie-Tooth diseaseAbdoulaye Yalcouyé, Adriana P Rebelo, Lassana Cissé, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 22, 2022
BiP inactivation due to loss of the deAMPylation function of FICD causes a motor neuron diseaseAdriana P Rebelo, Ariel Ruiz, Maike F Dohrn, et al.
Brain : a Journal of Neurology|April 23, 2021
A CADM3 variant causes Charcot-Marie-Tooth disease with marked upper limb involvementAdriana P Rebelo, Andrea Cortese, Amit Abraham, et al.
Neurology. Genetics|May 24, 2019
Autosomal dominant optic atrophy and cataract "plus" phenotype including axonal neuropathyAlejandro Horga, Enrico Bugiardini, Andreea Manole, et al.
Brain : a Journal of Neurology|May 26, 2021
Erratum to: A CADM3 variant causes Charcot-Marie-Tooth disease with marked upper limb involvementAdriana P Rebelo, Andrea Cortese, Amit Abraham, et al.
Pageof 7