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Wilson Marques

Showing results (91-100 of 197) with videos related to

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Muscle & Nerve|September 13, 2006
Expanding the phenotypes of the Pro56Ser VAPB mutation: proximal SMA with dysautonomiaVanessa D Marques, Amilton A Barreira, Mary B Davis, et al.
Journal of the Peripheral Nervous System : JPNS|April 3, 2012
Expanding the differential diagnosis of inherited neuropathies with non-uniform conduction: Andermann syndromeCharles M Lourenço, Nicolas Dupré, Jean-Baptiste Rivière, et al.
Journal of Neurology|April 24, 2015
Erratum to: Respiratory dysfunction in Charcot-Marie-Tooth disease type 1AMônica de Carvalho Alcântara, Marcello H Nogueira-Barbosa, Regina Maria França Fernandes, et al.
Clinical Nephrology|March 30, 2013
What lies beneath: Fabry nephropathy in a female patient with severe cerebrovascular diseaseElen A Romão, Charles M Lourenço, Wilson Marques Júnior, et al.
Journal of the Peripheral Nervous System : JPNS|April 30, 2020
High glucose level as a modifier factor in CMT1A patientsJuliana B Secchin, Rita C C Leal, Charles M Lourenço, et al.
Clinical Biomechanics (Bristol, Avon)|October 7, 2023
Vibration perception among children and adolescents with Charcot-Marie-tooth disease and implications for foot postureJuliana Cardoso, Cyntia Rogean de Jesus Alves de Baptista, Beatriz Parra Buzzetti, et al.
Arquivos De Neuro-Psiquiatria|May 13, 2025
A decade of whole-exome sequencing in Brazilian Neurology: from past insights to future perspectivesCaio Robledo D'Angioli Costa Quaio, Thiago Yoshinaga Tonholo Silva, Orlando G Barsottini, et al.
Journal of the Peripheral Nervous System : JPNS|February 20, 2024
Genetic diversity in hereditary axonal neuropathy: Analyzing 53 Brazilian childrenFernanda Barbosa Figueiredo, Pedro José Tomaselli, Jaime Hallak, et al.
Neuromuscular Disorders : NMD|April 27, 2021
GDAP1 mutations are frequent among Brazilian patients with autosomal recessive axonal Charcot-Marie-Tooth diseaseFernanda Barbosa Figueiredo, Wilson Araújo Silva, Silvana Giuliatti, et al.
Prague Medical Report|November 23, 2022
Amyotrophic Lateral Sclerosis: An Analysis of the Electromyographic Fatigue of the Masticatory MusclesLigia Maria Napolitano Gonçalves, Selma Siéssere, Flávia Argentato Cecilio, et al.
Pageof 20

Showing results (91-100 of 197) with videos related to

Sort By:
Pageof 20
Muscle & Nerve|September 13, 2006
Expanding the phenotypes of the Pro56Ser VAPB mutation: proximal SMA with dysautonomiaVanessa D Marques, Amilton A Barreira, Mary B Davis, et al.
Journal of the Peripheral Nervous System : JPNS|April 3, 2012
Expanding the differential diagnosis of inherited neuropathies with non-uniform conduction: Andermann syndromeCharles M Lourenço, Nicolas Dupré, Jean-Baptiste Rivière, et al.
Journal of Neurology|April 24, 2015
Erratum to: Respiratory dysfunction in Charcot-Marie-Tooth disease type 1AMônica de Carvalho Alcântara, Marcello H Nogueira-Barbosa, Regina Maria França Fernandes, et al.
Clinical Nephrology|March 30, 2013
What lies beneath: Fabry nephropathy in a female patient with severe cerebrovascular diseaseElen A Romão, Charles M Lourenço, Wilson Marques Júnior, et al.
Journal of the Peripheral Nervous System : JPNS|April 30, 2020
High glucose level as a modifier factor in CMT1A patientsJuliana B Secchin, Rita C C Leal, Charles M Lourenço, et al.
Clinical Biomechanics (Bristol, Avon)|October 7, 2023
Vibration perception among children and adolescents with Charcot-Marie-tooth disease and implications for foot postureJuliana Cardoso, Cyntia Rogean de Jesus Alves de Baptista, Beatriz Parra Buzzetti, et al.
Arquivos De Neuro-Psiquiatria|May 13, 2025
A decade of whole-exome sequencing in Brazilian Neurology: from past insights to future perspectivesCaio Robledo D'Angioli Costa Quaio, Thiago Yoshinaga Tonholo Silva, Orlando G Barsottini, et al.
Journal of the Peripheral Nervous System : JPNS|February 20, 2024
Genetic diversity in hereditary axonal neuropathy: Analyzing 53 Brazilian childrenFernanda Barbosa Figueiredo, Pedro José Tomaselli, Jaime Hallak, et al.
Neuromuscular Disorders : NMD|April 27, 2021
GDAP1 mutations are frequent among Brazilian patients with autosomal recessive axonal Charcot-Marie-Tooth diseaseFernanda Barbosa Figueiredo, Wilson Araújo Silva, Silvana Giuliatti, et al.
Prague Medical Report|November 23, 2022
Amyotrophic Lateral Sclerosis: An Analysis of the Electromyographic Fatigue of the Masticatory MusclesLigia Maria Napolitano Gonçalves, Selma Siéssere, Flávia Argentato Cecilio, et al.
Pageof 20