Unravelling Genetic Factors Underlying Corticobasal Syndrome: A Systematic Review.

Arienti, Federica; Lazzeri, Giulia; Vizziello, Maria; Monfrini, Edoardo; Bresolin, Nereo; Saetti, Maria Cristina; Picillo, Marina; Franco, Giulia; Di Fonzo, Alessio

Arienti, Federica; Lazzeri, Giulia; Vizziello, Maria; Monfrini, Edoardo; Bresolin, Nereo; Saetti, Maria Cristina; Picillo, Marina; Franco, Giulia; Di Fonzo, Alessio.

Arienti F; Dino Ferrari Center, Department of Pathophysiology and Transplantation, Neuroscience Section, University of Milan, 20122 Milan, Italy.
Lazzeri G; Dino Ferrari Center, Department of Pathophysiology and Transplantation, Neuroscience Section, University of Milan, 20122 Milan, Italy.
Vizziello M; Dino Ferrari Center, Department of Pathophysiology and Transplantation, Neuroscience Section, University of Milan, 20122 Milan, Italy.
Monfrini E; Dino Ferrari Center, Department of Pathophysiology and Transplantation, Neuroscience Section, University of Milan, 20122 Milan, Italy.
Bresolin N; Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neurology Unit, 20122 Milan, Italy.
Saetti MC; Dino Ferrari Center, Department of Pathophysiology and Transplantation, Neuroscience Section, University of Milan, 20122 Milan, Italy.
Picillo M; Center for Neurodegenerative Diseases, Department of Medicine, Surgery and Dentistry, Neuroscience Section, University of Salerno, 84084 Salerno, Italy.
Franco G; Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neurology Unit, 20122 Milan, Italy.
Di Fonzo A; Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neurology Unit, 20122 Milan, Italy.

Cells ; 10(1)2021 01 15.

Article en En | MEDLINE | ID: mdl-33467748

Asunto(s)

Enfermedades Neurodegenerativas/diagnóstico; Enfermedades Neurodegenerativas/genética; Trastornos Parkinsonianos/diagnóstico; Trastornos Parkinsonianos/genética; Edad de Inicio; Anciano; Afasia/diagnóstico; Afasia/genética; Proteína C9orf72/genética; Femenino; Estudios de Asociación Genética; Predisposición Genética a la Enfermedad; Humanos; Trastornos del Lenguaje/diagnóstico; Trastornos del Lenguaje/genética; Masculino; Trastornos Mentales/diagnóstico; Trastornos Mentales/genética; Persona de Mediana Edad; Mutación; Proteínas Priónicas/genética; Progranulinas/genética; Síndrome; Resultado del Tratamiento; Trastornos de la Visión/diagnóstico; Trastornos de la Visión/genética; Proteínas tau/genética

Palabras clave

CBS; atypical parkinsonism; corticobasal degeneration; corticobasal syndrome; genetics

Texto completo

Imprimir

XML

PubMed Links

Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades Neurodegenerativas / Trastornos Parkinsonianos Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Año: 2021 Tipo del documento: Article

Texto completo

Imprimir

XML

PubMed Links

Search on Google