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BMC Neuroscience
|
August 15, 2012
Identification of adequate vehicles to carry nerve regeneration inducers using tubulisation
Adriana 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 sclerosis
Lígia 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 disorders
Paulo 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 amyloidosis
Jemima 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 Brazil
Gustavo 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 patients
Guilherme 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 protein
Bruno 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 protein
Patrícia 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 cohort
Vivian Pedigone Cintra, Maike F Dohrn, Pedro José Tomaselli, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 30, 2026
POEMS syndrome: a neuromuscular perspective
Trajano Aguiar Pires Gonçalves, Camila Derminio Donadel, Rodrigo Siqueira Soares Frezatti, et al.
Page
of 20
Search research articles
Search
Showing results (111-120 of 197) with videos related to
Sort By:
Page
of 20
BMC Neuroscience
|
August 15, 2012
Identification of adequate vehicles to carry nerve regeneration inducers using tubulisation
Adriana 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 sclerosis
Lígia 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 disorders
Paulo 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 amyloidosis
Jemima 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 Brazil
Gustavo 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 patients
Guilherme 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 protein
Bruno 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 protein
Patrícia 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 cohort
Vivian Pedigone Cintra, Maike F Dohrn, Pedro José Tomaselli, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 30, 2026
POEMS syndrome: a neuromuscular perspective
Trajano Aguiar Pires Gonçalves, Camila Derminio Donadel, Rodrigo Siqueira Soares Frezatti, et al.
Page
of 20