Your browser doesn't support javascript.
loading
SCA1 patients may present as hereditary spastic paraplegia and must be included in spastic-ataxias group.
Pedroso, José Luiz; de Souza, Paulo Victor Sgobbi; Pinto, Wladimir Bocca Vieira de Rezende; Braga-Neto, Pedro; Albuquerque, Marcus Vinicius Cristino; Saraiva-Pereira, Maria Luiza; Jardim, Laura Bannach; Barsottini, Orlando Graziani Povoas.
Afiliación
  • Pedroso JL; Division of General Neurology and Ataxia Unit, Department of Neurology and Neurosurgery, Federal University of São Paulo (UNIFESP), São Paulo, Brazil. Electronic address: jlpedroso.neuro@gmail.com.
  • de Souza PV; Federal University of São Paulo (UNIFESP), São Paulo, Brazil.
  • Pinto WB; Neurology Residency Program, Department of Neurology and Neurosurgery, Federal University of São Paulo (UNIFESP), São Paulo, Brazil.
  • Braga-Neto P; Center of Health Sciences, Universidade Estadual do Ceará, CE, Brazil.
  • Albuquerque MV; Division of General Neurology and Ataxia Unit, Department of Neurology and Neurosurgery, Federal University of São Paulo (UNIFESP), São Paulo, Brazil.
  • Saraiva-Pereira ML; Department of Biochemistry, Universidade Federal do Rio Grande do Sul, Brazil; Medical Genetics Service, Hospital de Clínicas de Porto Alegre, Rio Grande do Sul, Brazil.
  • Jardim LB; Department of Internal Medicine, Universidade Federal do Rio Grande do Sul, Brazil; Medical Genetics Service, Hospital de Clínicas de Porto Alegre, Rio Grande do Sul, Brazil; Instituto Nacional de Genética Médica Populacional (INAGEMP), Porto Alegre, Brazil.
  • Barsottini OG; Division of General Neurology and Ataxia Unit, Department of Neurology and Neurosurgery, Federal University of São Paulo (UNIFESP), São Paulo, Brazil.
Parkinsonism Relat Disord ; 21(10): 1243-6, 2015 Oct.
Article en En | MEDLINE | ID: mdl-26231471
Asunto(s)
Palabras clave
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Paraplejía Espástica Hereditaria / Atrofia Óptica / Ataxias Espinocerebelosas / Discapacidad Intelectual / Espasticidad Muscular Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Parkinsonism Relat Disord Asunto de la revista: NEUROLOGIA Año: 2015 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Paraplejía Espástica Hereditaria / Atrofia Óptica / Ataxias Espinocerebelosas / Discapacidad Intelectual / Espasticidad Muscular Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Parkinsonism Relat Disord Asunto de la revista: NEUROLOGIA Año: 2015 Tipo del documento: Article