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Inherited metabolic diseases mimicking hereditary spastic paraplegia (HSP): a chance for treatment.
Teive, Hélio A G; Camargo, Carlos Henrique F; Pereira, Eduardo R; Coutinho, Léo; Munhoz, Renato P.
Afiliación
  • Teive HAG; Movement Disorders Unit, Neurology Service, Internal Medicine Department, Hospital de Clínicas, Federal University of Paraná, Rua General Carneiro 1103/102, Centro, Curitiba, Paraná, 80060-150, Brazil. hagteive@mps.com.br.
  • Camargo CHF; Neurological Diseases Group, Postgraduate Program of Internal Medicine, Hospital de Clínicas, Federal University of Paraná, Rua General Carneiro 1103/102, Centro, Curitiba, Paraná, 80060-150, Brazil. hagteive@mps.com.br.
  • Pereira ER; Neurological Diseases Group, Postgraduate Program of Internal Medicine, Hospital de Clínicas, Federal University of Paraná, Rua General Carneiro 1103/102, Centro, Curitiba, Paraná, 80060-150, Brazil.
  • Coutinho L; Neurological Diseases Group, Postgraduate Program of Internal Medicine, Hospital de Clínicas, Federal University of Paraná, Rua General Carneiro 1103/102, Centro, Curitiba, Paraná, 80060-150, Brazil.
  • Munhoz RP; Movement Disorders Unit, Neurology Service, Internal Medicine Department, Hospital de Clínicas, Federal University of Paraná, Rua General Carneiro 1103/102, Centro, Curitiba, Paraná, 80060-150, Brazil.
Neurogenetics ; 23(3): 167-177, 2022 07.
Article en En | MEDLINE | ID: mdl-35397036
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Paraplejía Espástica Hereditaria / Homocistinuria Tipo de estudio: Diagnostic_studies / Screening_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Neurogenetics Asunto de la revista: GENETICA / NEUROLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Brasil
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Paraplejía Espástica Hereditaria / Homocistinuria Tipo de estudio: Diagnostic_studies / Screening_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Neurogenetics Asunto de la revista: GENETICA / NEUROLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Brasil