Your browser doesn't support javascript.
loading
Clinical, ophthalmological, imaging and genetic features in Brazilian patients with ARSACS.
Rezende Filho, Flávio Moura; Parkinson, Michael H; Pedroso, José Luiz; Poh, Roy; Faber, Ingrid; Lourenço, Charles Marques; Júnior, Wilson Marques; França Junior, Marcondes Cavalcante; Kok, Fernando; Sallum, Juliana M Ferraz; Giunti, Paola; Barsottini, Orlando Graziani Póvoas.
Afiliación
  • Rezende Filho FM; Division of General Neurology and Ataxia Unit, Department of Neurology, Universidade Federal de São Paulo, Sao Paulo, SP, Brazil.
  • Parkinson MH; Department of Movement and Clinical Neurosciences, UCL Queen Square Institute of Neurology London, UK.
  • Pedroso JL; Division of General Neurology and Ataxia Unit, Department of Neurology, Universidade Federal de São Paulo, Sao Paulo, SP, Brazil.
  • Poh R; Laboratory of Neurogenetics, NHNN, UCLH Queen Square London, UK.
  • Faber I; Department of Neurology, Universidade Estadual de Campinas, Campinas, SP, Brazil.
  • Lourenço CM; Department of Neurology, University of São Paulo, School of Medicine, Ribeirão Preto, SP, Brazil.
  • Júnior WM; Department of Neurology, University of São Paulo, School of Medicine, Ribeirão Preto, SP, Brazil.
  • França Junior MC; Department of Neurology, Universidade Estadual de Campinas, Campinas, SP, Brazil.
  • Kok F; Mendelics Genomic Analysis, São Paulo, SP, Brazil; Department of Neurology, University of São Paulo, School of Medicine, São Paulo, SP, Brazil.
  • Sallum JMF; Department of Ophthalmology, Universidade Federal de São Paulo, Sao Paulo, SP, Brazil.
  • Giunti P; Department of Movement and Clinical Neurosciences, UCL Queen Square Institute of Neurology London, UK. Electronic address: p.giunti@ucl.ac.uk.
  • Barsottini OGP; Division of General Neurology and Ataxia Unit, Department of Neurology, Universidade Federal de São Paulo, Sao Paulo, SP, Brazil.
Parkinsonism Relat Disord ; 62: 148-155, 2019 05.
Article en En | MEDLINE | ID: mdl-30638817

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Imagen por Resonancia Magnética / Análisis de Secuencia de ADN / Ataxias Espinocerebelosas / Tomografía de Coherencia Óptica / Neuronas Retinianas / Espasticidad Muscular Tipo de estudio: Guideline / Qualitative_research Límite: Adolescent / Adult / Female / Humans / Male / Middle aged País/Región como asunto: America do sul / Brasil Idioma: En Revista: Parkinsonism Relat Disord Asunto de la revista: NEUROLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Brasil

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Imagen por Resonancia Magnética / Análisis de Secuencia de ADN / Ataxias Espinocerebelosas / Tomografía de Coherencia Óptica / Neuronas Retinianas / Espasticidad Muscular Tipo de estudio: Guideline / Qualitative_research Límite: Adolescent / Adult / Female / Humans / Male / Middle aged País/Región como asunto: America do sul / Brasil Idioma: En Revista: Parkinsonism Relat Disord Asunto de la revista: NEUROLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Brasil
...