Cargando…
Neuromuscular choristoma: a rare cause of congenital non-progressive lower limb amyotrophy
Autores principales: | MACHADO, Roberta Ismael Lacerda, de ALBURQUERQUE, José Marcos Vieira, de SOUZA, Paulo Victor Sgobbi, AIVAZOGLOU, Laís Uyeda, BADIA, Bruno de Mattos Lombardi, OGATA, Stéphanie Yuri Torres, FARIAS, Igor Braga, AIHARA, André Yui, FERNANDES, Artur da Rocha Corrêa, PINTO, Wladimir Bocca Vieira de Rezende, OLIVEIRA, Acary Souza Bulle |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Academia Brasileira de Neurologia - ABNEURO
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9394553/ https://www.ncbi.nlm.nih.gov/pubmed/34037103 http://dx.doi.org/10.1590/0004-282X-ANP-2020-0370 |
Ejemplares similares
Cargando…
Neuralgic amyotrophy: an underrecognized entity
por: Kim, Tae Uk, et al.
Publicado: (2021)
por: Kim, Tae Uk, et al.
Publicado: (2021)
Ejemplares similares
-
Acute Hepatic Porphyria: Pathophysiological Basis of Neuromuscular Manifestations
por: de Souza, Paulo Victor Sgobbi, et al.
Publicado: (2021) -
Editorial: The expanding clinical and genetic basis of adult inherited neurometabolic disorders
por: Pinto, Wladimir Bocca Vieira de Rezende, et al.
Publicado: (2023) -
Brazilian registry of patients with porphyria: REBRAPPO study
por: Souza, Paulo Victor Sgobbi, et al.
Publicado: (2023) -
Should we investigate mitochondrial disorders in progressive adult-onset undetermined ataxias?
por: Pedroso, José Luiz, et al.
Publicado: (2020) -
Progressive spastic tetraplegia and axial hypotonia (STAHP) due to SOD1 deficiency: is it really a new entity?
por: de Souza, Paulo Victor Sgobbi, et al.
Publicado: (2021)