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 (81-90 of 197) with videos related to

Pageof 20
Sort By:
Arquivos De Neuro-Psiquiatria|March 17, 2016
Clinical and neurophysiological features of the hereditary neuropathy with liability to pressure palsy due to the 17p11.2 deletionAline Pinheiro Martins de Oliveira, Raquel Campos Pereira, Patrícia Toscano Onofre, et al.
Cerebellum (London, England)|July 15, 2023
Genetic Epidemiology and Clinical Characteristics of Patients with Spinocerebellar Ataxias in an Unexplored Brazilian State, Using Strategies for Resource-Limited SettingsDébora Beserra Vilar Moraes, Tácio Luis Cavalcante Coradine, Everton Vieira Lopes Silva, et al.
Muscle & Nerve|September 30, 2010
Coexistence of two chronic neuropathies in a young child: Charcot-Marie-Tooth disease type 1A and chronic inflammatory demyelinating polyneuropathyWilson Marques, Carolina A R Funayama, Juliana B Secchin, et al.
Practical Neurology|June 24, 2025
Pachymeningeal thickening and subdural effusion in POEMS syndromeTrajano Aguiar Pires Gonçalves, Camila Dermínio Donadel, Rodrigo Siqueira Soares Frezatti, et al.
Physiotherapy Theory and Practice|May 4, 2019
Physical function and performance measures of children and adolescents with Charcot-Marie-Tooth diseaseCyntia Rogean De Baptista, Adriana H Nascimento-Elias, Beatriz Garcia, et al.
Cerebellum (London, England)|August 18, 2022
Voxel-Based Morphometry and Relaxometry Demonstrate Macro- and Microstructural Damages in Spinocerebellar Ataxia Type 3Lívia Leite Góes Gitaí, Manoel Alves Sobreira-Neto, Paula Rejane Beserra Diniz, et al.
Pediatric Neurology|December 3, 2024
Hopkins Syndrome: An Uncommon Cause of Weakness in Intensive Care UnitTrajano Aguiar Pires Gonçalves, Maria Clara Zanon Zotin, Carolina Lavigne Moreira, et al.
Journal of the Peripheral Nervous System : JPNS|June 14, 2024
Monoclonal gammopathy-associated peripheral neuropathies: Uncovering pearls and challengesTrajano Aguiar Pires Gonçalves, Camila Derminio Donadel, Rodrigo Siqueira Soares Frezatti, et al.
Cerebellum (London, England)|September 18, 2020
Which Factors in Spinocerebellar Ataxia Type 3 Patients Are Associated with Restless Legs Syndrome/Willis-Ekbom Disease?Lívia Leite Góes Gitaí, Alan Luiz Éckeli, Manoel Alves Sobreira-Neto, et al.
Journal of Neurology|March 13, 2015
Respiratory dysfunction in Charcot-Marie-Tooth disease type 1AMônica de Carvalho Alcântara, Marcello H Nogueira-Barbosa, Regina Maria França Fernandes, et al.
Pageof 20

Showing results (81-90 of 197) with videos related to

Sort By:
Pageof 20
Arquivos De Neuro-Psiquiatria|March 17, 2016
Clinical and neurophysiological features of the hereditary neuropathy with liability to pressure palsy due to the 17p11.2 deletionAline Pinheiro Martins de Oliveira, Raquel Campos Pereira, Patrícia Toscano Onofre, et al.
Cerebellum (London, England)|July 15, 2023
Genetic Epidemiology and Clinical Characteristics of Patients with Spinocerebellar Ataxias in an Unexplored Brazilian State, Using Strategies for Resource-Limited SettingsDébora Beserra Vilar Moraes, Tácio Luis Cavalcante Coradine, Everton Vieira Lopes Silva, et al.
Muscle & Nerve|September 30, 2010
Coexistence of two chronic neuropathies in a young child: Charcot-Marie-Tooth disease type 1A and chronic inflammatory demyelinating polyneuropathyWilson Marques, Carolina A R Funayama, Juliana B Secchin, et al.
Practical Neurology|June 24, 2025
Pachymeningeal thickening and subdural effusion in POEMS syndromeTrajano Aguiar Pires Gonçalves, Camila Dermínio Donadel, Rodrigo Siqueira Soares Frezatti, et al.
Physiotherapy Theory and Practice|May 4, 2019
Physical function and performance measures of children and adolescents with Charcot-Marie-Tooth diseaseCyntia Rogean De Baptista, Adriana H Nascimento-Elias, Beatriz Garcia, et al.
Cerebellum (London, England)|August 18, 2022
Voxel-Based Morphometry and Relaxometry Demonstrate Macro- and Microstructural Damages in Spinocerebellar Ataxia Type 3Lívia Leite Góes Gitaí, Manoel Alves Sobreira-Neto, Paula Rejane Beserra Diniz, et al.
Pediatric Neurology|December 3, 2024
Hopkins Syndrome: An Uncommon Cause of Weakness in Intensive Care UnitTrajano Aguiar Pires Gonçalves, Maria Clara Zanon Zotin, Carolina Lavigne Moreira, et al.
Journal of the Peripheral Nervous System : JPNS|June 14, 2024
Monoclonal gammopathy-associated peripheral neuropathies: Uncovering pearls and challengesTrajano Aguiar Pires Gonçalves, Camila Derminio Donadel, Rodrigo Siqueira Soares Frezatti, et al.
Cerebellum (London, England)|September 18, 2020
Which Factors in Spinocerebellar Ataxia Type 3 Patients Are Associated with Restless Legs Syndrome/Willis-Ekbom Disease?Lívia Leite Góes Gitaí, Alan Luiz Éckeli, Manoel Alves Sobreira-Neto, et al.
Journal of Neurology|March 13, 2015
Respiratory dysfunction in Charcot-Marie-Tooth disease type 1AMônica de Carvalho Alcântara, Marcello H Nogueira-Barbosa, Regina Maria França Fernandes, et al.
Pageof 20