Atypical clinical presentation and typical FTD atrophy: 17-year clinical follow-up and MRI analysis of a slowly progressive bvFTD associated with C9orf72 expansion.

Géraudie, A; Guerrier, L; Le Ber, I; Clot, F; Péran, P; Pariente, J

Géraudie, A; Guerrier, L; Le Ber, I; Clot, F; Péran, P; Pariente, J.

Afiliação

Géraudie A; Department of neurology, Toulouse university hospital, Toulouse, France. Electronic address: geraudie.a@chu-toulouse.fr.
Guerrier L; Inserm, UPS, ToNIC, Toulouse NeuroImaging Centre, university of Toulouse, Toulouse, France.
Le Ber I; Inserm U 1127, CNRS UMR 7225, ICM Brain and Spine Institute, Sorbonne université, Paris, France; Centre de référence des démences rares, hôpital de la Pitié-Salpêtrière, Assistance publique-Hôpitaux de Paris (AP-HP), Paris, France.
Clot F; UF de neurogénétique moléculaire et cellulaire, département de génétique, hôpitaux universitaires La-Pitié-Salpêtrière-Charles Foix, AP-HP, Paris, France.
Péran P; Inserm, UPS, ToNIC, Toulouse NeuroImaging Centre, university of Toulouse, Toulouse, France.
Pariente J; Department of neurology, Toulouse university hospital, Toulouse, France; Inserm, UPS, ToNIC, Toulouse NeuroImaging Centre, university of Toulouse, Toulouse, France.

Rev Neurol (Paris) ; 176(7-8): 627-629, 2020 09.

Article em En | MEDLINE | ID: mdl-32178877

Assuntos

Esclerose Lateral Amiotrófica; Demência Frontotemporal; Esclerose Lateral Amiotrófica/genética; Atrofia; Proteína C9orf72/genética; Expansão das Repetições de DNA; Seguimentos; Demência Frontotemporal/genética; Humanos; Imageamento por Ressonância Magnética

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Demência Frontotemporal / Esclerose Lateral Amiotrófica Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Rev Neurol (Paris) Ano de publicação: 2020 Tipo de documento: Article

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