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Wilson Marques

Showing results (111-120 of 197) with videos related to

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BMC Neuroscience|August 15, 2012
Identification of adequate vehicles to carry nerve regeneration inducers using tubulisationAdriana Helena do Nascimento-Elias, Bruno César Fresnesdas, Maria Cristina Lopes Schiavoni, et al.
Journal of Applied Oral Science : Revista FOB|June 14, 2018
Alterations in the stomatognathic system due to amyotrophic lateral sclerosisLígia Maria Napolitano Gonçalves, Marcelo Palinkas, Jaime Eduardo Cecilio Hallak, et al.
Journal of Neurology|April 9, 2025
Distinct patterns of cerebral and spinal pathology along the spectrum of ATXN2-related disordersPaulo Schneider Wolmer, Fabrício Castro de Borba, Thiago Junqueira Ribeiro de Rezende, et al.
European Journal of Medical Genetics|May 17, 2022
Involvement of cranial nerves in ATTR Ile127Val amyloidosisJemima A da Silva Batista, Luiza R Carrera, Adriele R F Viriato, et al.
Journal of the Peripheral Nervous System : JPNS|January 7, 2026
Genetic and Clinical Spectrum of Hereditary Transthyretin Amyloidosis in BrazilGustavo Maximiano-Alves, Carolina Lavigne-Moreira, Marcus Vinicius Simões, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 26, 2008
Huntington's disease-like 2 in Brazil--report of 4 patientsGuilherme G Riccioppo Rodrigues, Ruth H Walker, Alexis Brice, et al.
Neuroscience Letters|February 8, 2005
Normal brain mitochondrial respiration in adult mice lacking cellular prion proteinBruno Lobão-Soares, Marino Muxfeldt Bianchin, Marcelo Neves Linhares, et al.
Neuroscience Letters|July 26, 2005
Impaired exercise capacity, but unaltered mitochondrial respiration in skeletal or cardiac muscle of mice lacking cellular prion proteinPatrícia Barreto Costa Nico, Bruno Lobão-Soares, Michele Christine Landemberger, et al.
Journal of the Neurological Sciences|June 5, 2021
Rare mutations in ATL3, SPTLC2 and SCN9A explaining hereditary sensory neuropathy and congenital insensitivity to pain in a Brazilian cohortVivian Pedigone Cintra, Maike F Dohrn, Pedro José Tomaselli, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 30, 2026
POEMS syndrome: a neuromuscular perspectiveTrajano Aguiar Pires Gonçalves, Camila Derminio Donadel, Rodrigo Siqueira Soares Frezatti, et al.
Pageof 20

Showing results (111-120 of 197) with videos related to

Sort By:
Pageof 20
BMC Neuroscience|August 15, 2012
Identification of adequate vehicles to carry nerve regeneration inducers using tubulisationAdriana Helena do Nascimento-Elias, Bruno César Fresnesdas, Maria Cristina Lopes Schiavoni, et al.
Journal of Applied Oral Science : Revista FOB|June 14, 2018
Alterations in the stomatognathic system due to amyotrophic lateral sclerosisLígia Maria Napolitano Gonçalves, Marcelo Palinkas, Jaime Eduardo Cecilio Hallak, et al.
Journal of Neurology|April 9, 2025
Distinct patterns of cerebral and spinal pathology along the spectrum of ATXN2-related disordersPaulo Schneider Wolmer, Fabrício Castro de Borba, Thiago Junqueira Ribeiro de Rezende, et al.
European Journal of Medical Genetics|May 17, 2022
Involvement of cranial nerves in ATTR Ile127Val amyloidosisJemima A da Silva Batista, Luiza R Carrera, Adriele R F Viriato, et al.
Journal of the Peripheral Nervous System : JPNS|January 7, 2026
Genetic and Clinical Spectrum of Hereditary Transthyretin Amyloidosis in BrazilGustavo Maximiano-Alves, Carolina Lavigne-Moreira, Marcus Vinicius Simões, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 26, 2008
Huntington's disease-like 2 in Brazil--report of 4 patientsGuilherme G Riccioppo Rodrigues, Ruth H Walker, Alexis Brice, et al.
Neuroscience Letters|February 8, 2005
Normal brain mitochondrial respiration in adult mice lacking cellular prion proteinBruno Lobão-Soares, Marino Muxfeldt Bianchin, Marcelo Neves Linhares, et al.
Neuroscience Letters|July 26, 2005
Impaired exercise capacity, but unaltered mitochondrial respiration in skeletal or cardiac muscle of mice lacking cellular prion proteinPatrícia Barreto Costa Nico, Bruno Lobão-Soares, Michele Christine Landemberger, et al.
Journal of the Neurological Sciences|June 5, 2021
Rare mutations in ATL3, SPTLC2 and SCN9A explaining hereditary sensory neuropathy and congenital insensitivity to pain in a Brazilian cohortVivian Pedigone Cintra, Maike F Dohrn, Pedro José Tomaselli, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 30, 2026
POEMS syndrome: a neuromuscular perspectiveTrajano Aguiar Pires Gonçalves, Camila Derminio Donadel, Rodrigo Siqueira Soares Frezatti, et al.
Pageof 20