Phenotype and imaging features associated with APP duplications

BACKGROUND: APP duplication is a rare genetic cause of Alzheimer disease and cerebral amyloid angiopathy (CAA). We aimed to evaluate the phenotypes of APP duplications carriers. METHODS: Clinical, radiological, and neuropathological features of 43 APP duplication carriers from 24 French families wer...

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Detalles Bibliográficos
Autores principales: Grangeon, Lou, Charbonnier, Camille, Zarea, Aline, Rousseau, Stephane, Rovelet-Lecrux, Anne, Bendetowicz, David, Lemaitre, Marion, Malrain, Cécile, Quillard-Muraine, Muriel, Cassinari, Kevin, Maltete, David, Pariente, Jeremie, Moreaud, Olivier, Magnin, Eloi, Cretin, Benjamin, Mackowiak, Marie-Anne, Sillaire, Adeline Rollin, Vercelletto, Martine, Dionet, Elsa, Felician, Olivier, Rod-Olivieri, Pauline, Thomas-Antérion, Catherine, Godeneche, Gaelle, Sauvée, Mathilde, Cartz-Piver, Leslie, Le Ber, Isabelle, Chauvire, Valérie, Jonveaux, Therèse, Balageas, Anna-Chloé, Laquerriere, Annie, Duyckaerts, Charles, Vital, Anne, de Paula, Andre Maues, Meyronet, David, Guyant-Marechal, Lucie, Hannequin, Didier, Tournier-Lasserve, Elisabeth, Campion, Dominique, Nicolas, Gaël, Wallon, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10173644/
https://www.ncbi.nlm.nih.gov/pubmed/37170141
http://dx.doi.org/10.1186/s13195-023-01172-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10173644/
https://www.ncbi.nlm.nih.gov/pubmed/37170141
http://dx.doi.org/10.1186/s13195-023-01172-2

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