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Paraparesia espástica hereditaria por mutación en SPG5/CYP7B1 con potenciales implicaciones terapéuticas / Hereditary spastic paraparesis due to SPG5/CYP7B1 mutation with potential therapeutic implications
Pérez-Torre, P; García Galloway, E; López-Sendón Moreno, J. L.
Affiliation
  • Pérez-Torre, P; Hospital Universitario Ramón y Cajal. Servicio de Neurología. Madrid. España
  • García Galloway, E; Hospital Universitario Ramón y Cajal. Servicio de Genética. Madrid. España
  • López-Sendón Moreno, J. L; Hospital Universitario Ramón y Cajal. Servicio de Neurología. Madrid. España
Neurología (Barc., Ed. impr.) ; 38(9): 710-711, Nov-Dic. 2023. ilus
Article in Spanish | IBECS | ID: ibc-227355
Responsible library: ES1.1
Localization: ES15.1 - BNCS
Subject(s)
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Full text: Available Collection: National databases / Spain Database: IBECS Main subject: Therapeutics / Gait Disorders, Neurologic / Paraparesis, Spastic / Lower Extremity / Atorvastatin / Muscle Spasticity Limits: Female / Humans / Male Language: Spanish Journal: Neurología (Barc., Ed. impr.) Year: 2023 Document type: Article Institution/Affiliation country: Hospital Universitario Ramón y Cajal/España
Fulltext
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Full text: Available Collection: National databases / Spain Database: IBECS Main subject: Therapeutics / Gait Disorders, Neurologic / Paraparesis, Spastic / Lower Extremity / Atorvastatin / Muscle Spasticity Limits: Female / Humans / Male Language: Spanish Journal: Neurología (Barc., Ed. impr.) Year: 2023 Document type: Article Institution/Affiliation country: Hospital Universitario Ramón y Cajal/España