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

Wilson Marques

Showing results (171-180 of 197) with videos related to

Pageof 20
Sort By:
Parkinsonism & Related Disorders|October 26, 2021
DRPLA: An unusual disease or an underestimated cause of ataxia in Brazil?Wladimir Bocca Vieira de Rezende Pinto, Rubens Paulo Araújo Salomão, Nathália Cabral Bergamasco, et al.
Brain : a Journal of Neurology|May 12, 2023
Biallelic variants in COQ7 cause distal hereditary motor neuropathy with upper motor neuron signsAdriana P Rebelo, Pedro J Tomaselli, Jessica Medina, et al.
Arquivos De Neuro-Psiquiatria|April 14, 2023
Brazilian consensus for diagnosis, management and treatment of hereditary transthyretin amyloidosis with peripheral neuropathy: second editionMarcus Vinicius Pinto, Marcondes Cavalcante França, Marcus Vinicius Magno Gonçalves, et al.
Arquivos De Neuro-Psiquiatria|July 28, 2025
Brazilian Academy of Neurology recommendations for diagnosis, management, and treatment of chronic inflammatory demyelinating polyradiculoneuropathy (CIDP)Osvaldo J M Nascimento, Wilson Marques, Marcus Vinícius Magno Gonçalves, et al.
Neurogenetics|October 4, 2011
New mutations in the ATM gene and clinical data of 25 AT patientsIlja Demuth, Véronique Dutrannoy, Wilson Marques, et al.
American Journal of Human Genetics|June 11, 2013
Alteration of ganglioside biosynthesis responsible for complex hereditary spastic paraplegiaAmir Boukhris, Rebecca Schule, José L Loureiro, et al.
Journal of the Neurological Sciences|April 28, 2020
CAG repeats ≥ 34 in Ataxin-1 gene are associated with amyotrophic lateral sclerosis in a Brazilian cohortJoão Pedro Nunes Gonçalves, Helen Maia Tavares de Andrade, Vívian Pedigone Cintra, et al.
Human Mutation|July 17, 2013
Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12Guida Landouré, Peng-Peng Zhu, Charles M Lourenço, et al.
JAMA|September 28, 2023
Eplontersen for Hereditary Transthyretin Amyloidosis With PolyneuropathyTeresa Coelho, Wilson Marques, Noel R Dasgupta, et al.
Brain : a Journal of Neurology|November 11, 2017
Hereditary spastic paraplegia type 5: natural history, biomarkers and a randomized controlled trialLudger Schöls, Tim W Rattay, Peter Martus, et al.
Pageof 20

Showing results (171-180 of 197) with videos related to

Sort By:
Pageof 20
Parkinsonism & Related Disorders|October 26, 2021
DRPLA: An unusual disease or an underestimated cause of ataxia in Brazil?Wladimir Bocca Vieira de Rezende Pinto, Rubens Paulo Araújo Salomão, Nathália Cabral Bergamasco, et al.
Brain : a Journal of Neurology|May 12, 2023
Biallelic variants in COQ7 cause distal hereditary motor neuropathy with upper motor neuron signsAdriana P Rebelo, Pedro J Tomaselli, Jessica Medina, et al.
Arquivos De Neuro-Psiquiatria|April 14, 2023
Brazilian consensus for diagnosis, management and treatment of hereditary transthyretin amyloidosis with peripheral neuropathy: second editionMarcus Vinicius Pinto, Marcondes Cavalcante França, Marcus Vinicius Magno Gonçalves, et al.
Arquivos De Neuro-Psiquiatria|July 28, 2025
Brazilian Academy of Neurology recommendations for diagnosis, management, and treatment of chronic inflammatory demyelinating polyradiculoneuropathy (CIDP)Osvaldo J M Nascimento, Wilson Marques, Marcus Vinícius Magno Gonçalves, et al.
Neurogenetics|October 4, 2011
New mutations in the ATM gene and clinical data of 25 AT patientsIlja Demuth, Véronique Dutrannoy, Wilson Marques, et al.
American Journal of Human Genetics|June 11, 2013
Alteration of ganglioside biosynthesis responsible for complex hereditary spastic paraplegiaAmir Boukhris, Rebecca Schule, José L Loureiro, et al.
Journal of the Neurological Sciences|April 28, 2020
CAG repeats ≥ 34 in Ataxin-1 gene are associated with amyotrophic lateral sclerosis in a Brazilian cohortJoão Pedro Nunes Gonçalves, Helen Maia Tavares de Andrade, Vívian Pedigone Cintra, et al.
Human Mutation|July 17, 2013
Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12Guida Landouré, Peng-Peng Zhu, Charles M Lourenço, et al.
JAMA|September 28, 2023
Eplontersen for Hereditary Transthyretin Amyloidosis With PolyneuropathyTeresa Coelho, Wilson Marques, Noel R Dasgupta, et al.
Brain : a Journal of Neurology|November 11, 2017
Hereditary spastic paraplegia type 5: natural history, biomarkers and a randomized controlled trialLudger Schöls, Tim W Rattay, Peter Martus, et al.
Pageof 20