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Gait & Posture
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March 13, 2021
Dynamic plantar pressure patterns in children and adolescents with Charcot-Marie-Tooth disease
Juliana Cardoso, Cyntia R J Alves de Baptista, Cristina D Sartor, et al.
Neuromuscular Disorders : NMD
|
May 3, 2011
Characterizing the phenotypic manifestations of MFN2 R104W mutation in Charcot-Marie-Tooth type 2
Adriana Borges Genari, Vinícius Horácio Stefani Borghetti, Silmara Paula Gouvêa, et al.
Journal of the Peripheral Nervous System : JPNS
|
February 1, 2023
Inter-rater reliability of the Rasch-modified medical research council scoring criteria for manual muscle testing in neuromuscular diseases
Rodrigo Melo Conde, Lívia de Almeida Pereira Pena, Adriana Helena do Nascimento Elias, et al.
Journal of the Peripheral Nervous System : JPNS
|
October 3, 2025
The Easy Handgrip Test as a Tool for Assessing Motor Fatigability in Children With Charcot-Marie-Tooth Disease Type 1A
Ester da Silva Estevam, Emanuela Juvenal Martins, Camila Scarpino Barboza Franco, et al.
Cerebellum (London, England)
|
March 23, 2024
Prevalence and Diagnostic Journey of Friedreich's Ataxia in the State of São Paulo, Brazil
Daiana Suelen Machado, Celiana Figueiredo Viana, José Luiz Pedroso, et al.
The Brazilian Journal of Infectious Diseases : an Official Publication of the Brazilian Society of Infectious Diseases
|
May 15, 2025
RIMOXCLAMIN: New therapeutic regimen for Hansen's Disease cure based on effective sensitivity recovery
Marco Andrey Cipriani Frade, Gustavo Sartori Albertino, Filipe Rocha Lima, et al.
Journal of the Peripheral Nervous System : JPNS
|
March 10, 2018
The genetic heterogeneity of hereditary transthyretin amyloidosis in a sample of the Brazilian population
Carolina Lavigne-Moreira, Vanessa D Marques, Marcus V M Gonçalves, et al.
Journal of Human Genetics
|
April 10, 2020
Presence of val30Met and val122ile mutations in a patient with hereditary amyloidosis
Jemima A da Silva-Batista, Wilson Marques, Mayala Thayrine de J S Oliveira, et al.
Neurology. Genetics
|
April 12, 2016
Mutation in PNKP presenting initially as axonal Charcot-Marie-Tooth disease
José Luiz Pedroso, Clarissa R R Rocha, Lucia I Macedo-Souza, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
November 5, 2024
Exploring cognitive functions and brain structure in Hereditary Transthyretin amyloidosis using brain MRI and neuropsychological assessment
Iara Senem, Maria Paula Foss, Carolina Lavigne-Moreira, et al.
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of 20
Search research articles
Search
Showing results (101-110 of 197) with videos related to
Sort By:
Page
of 20
Gait & Posture
|
March 13, 2021
Dynamic plantar pressure patterns in children and adolescents with Charcot-Marie-Tooth disease
Juliana Cardoso, Cyntia R J Alves de Baptista, Cristina D Sartor, et al.
Neuromuscular Disorders : NMD
|
May 3, 2011
Characterizing the phenotypic manifestations of MFN2 R104W mutation in Charcot-Marie-Tooth type 2
Adriana Borges Genari, Vinícius Horácio Stefani Borghetti, Silmara Paula Gouvêa, et al.
Journal of the Peripheral Nervous System : JPNS
|
February 1, 2023
Inter-rater reliability of the Rasch-modified medical research council scoring criteria for manual muscle testing in neuromuscular diseases
Rodrigo Melo Conde, Lívia de Almeida Pereira Pena, Adriana Helena do Nascimento Elias, et al.
Journal of the Peripheral Nervous System : JPNS
|
October 3, 2025
The Easy Handgrip Test as a Tool for Assessing Motor Fatigability in Children With Charcot-Marie-Tooth Disease Type 1A
Ester da Silva Estevam, Emanuela Juvenal Martins, Camila Scarpino Barboza Franco, et al.
Cerebellum (London, England)
|
March 23, 2024
Prevalence and Diagnostic Journey of Friedreich's Ataxia in the State of São Paulo, Brazil
Daiana Suelen Machado, Celiana Figueiredo Viana, José Luiz Pedroso, et al.
The Brazilian Journal of Infectious Diseases : an Official Publication of the Brazilian Society of Infectious Diseases
|
May 15, 2025
RIMOXCLAMIN: New therapeutic regimen for Hansen's Disease cure based on effective sensitivity recovery
Marco Andrey Cipriani Frade, Gustavo Sartori Albertino, Filipe Rocha Lima, et al.
Journal of the Peripheral Nervous System : JPNS
|
March 10, 2018
The genetic heterogeneity of hereditary transthyretin amyloidosis in a sample of the Brazilian population
Carolina Lavigne-Moreira, Vanessa D Marques, Marcus V M Gonçalves, et al.
Journal of Human Genetics
|
April 10, 2020
Presence of val30Met and val122ile mutations in a patient with hereditary amyloidosis
Jemima A da Silva-Batista, Wilson Marques, Mayala Thayrine de J S Oliveira, et al.
Neurology. Genetics
|
April 12, 2016
Mutation in PNKP presenting initially as axonal Charcot-Marie-Tooth disease
José Luiz Pedroso, Clarissa R R Rocha, Lucia I Macedo-Souza, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
November 5, 2024
Exploring cognitive functions and brain structure in Hereditary Transthyretin amyloidosis using brain MRI and neuropsychological assessment
Iara Senem, Maria Paula Foss, Carolina Lavigne-Moreira, et al.
Page
of 20