Frequency and Longitudinal Course of Motor Signs in Genetic Frontotemporal Dementia

BACKGROUND AND OBJECTIVES: Frontotemporal dementia (FTD) is a highly heritable disorder. The majority of genetic cases are caused by autosomal dominant pathogenic variants in the chromosome 9 open reading frame 72 (c9orf72), progranulin (GRN), and microtubule-associated protein tau (MAPT) gene. As m...

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Detalles Bibliográficos
Autores principales: Schönecker, Sonja, Martinez-Murcia, Francisco J., Rauchmann, Boris-Stephan, Franzmeier, Nicolai, Prix, Catharina, Wlasich, Elisabeth, Loosli, Sandra V., Bochmann, Katja, Gorriz Saez, Juan-Manuel, Laforce, Robert, Ducharme, Simon, Tartaglia, Maria Carmela, Finger, Elizabeth, de Mendonça, Alexandre, Santana, Isabel, Sanchez-Valle, Raquel, Moreno, Fermin, Sorbi, Sandro, Tagliavini, Fabrizio, Borroni, Barbara, Otto, Markus, Synofzik, Matthis, Galimberti, Daniela, Vandenberghe, Rik, van Swieten, John, Butler, Christopher, Gerhard, Alexander, Graff, Caroline, Danek, Adrian, Rohrer, Jonathan D., Masellis, Mario, Rowe, James, Levin, Johannes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9519250/
https://www.ncbi.nlm.nih.gov/pubmed/35948443
http://dx.doi.org/10.1212/WNL.0000000000200828

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9519250/
https://www.ncbi.nlm.nih.gov/pubmed/35948443
http://dx.doi.org/10.1212/WNL.0000000000200828

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