Brain volumetric deficits in MAPT mutation carriers: a multisite study

OBJECTIVE: MAPT mutations typically cause behavioral variant frontotemporal dementia with or without parkinsonism. Previous studies have shown that symptomatic MAPT mutation carriers have frontotemporal atrophy, yet studies have shown mixed results as to whether presymptomatic carriers have low gray...

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Detalles Bibliográficos
Autores principales: Chu, Stephanie A., Flagan, Taru M., Staffaroni, Adam M., Jiskoot, Lize C., Deng, Jersey, Spina, Salvatore, Zhang, Liwen, Sturm, Virginia E., Yokoyama, Jennifer S., Seeley, William W., Papma, Janne M., Geschwind, Dan H., Rosen, Howard J., Boeve, Bradley F., Boxer, Adam L., Heuer, Hilary W., Forsberg, Leah K., Brushaber, Danielle E., Grossman, Murray, Coppola, Giovanni, Dickerson, Bradford C., Bordelon, Yvette M., Faber, Kelley, Feldman, Howard H., Fields, Julie A., Fong, Jamie C., Foroud, Tatiana, Gavrilova, Ralitza H., Ghoshal, Nupur, Graff‐Radford, Neill R., Hsiung, Ging‐Yuek Robin, Huey, Edward D., Irwin, David J., Kantarci, Kejal, Kaufer, Daniel I., Karydas, Anna M., Knopman, David S., Kornak, John, Kramer, Joel H., Kukull, Walter A., Lapid, Maria I., Litvan, Irene, Mackenzie, Ian R.A., Mendez, Mario F., Miller, Bruce L., Onyike, Chiadi U., Pantelyat, Alexander Y., Rademakers, Rosa, Marisa Ramos, Eliana, Roberson, Erik D., Carmela Tartaglia, Maria, Tatton, Nadine A., Toga, Arthur W., Vetor, Ashley, Weintraub, Sandra, Wong, Bonnie, Wszolek, Zbigniew K., Van Swieten, John C., Lee, Suzee E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7818091/
https://www.ncbi.nlm.nih.gov/pubmed/33247623
http://dx.doi.org/10.1002/acn3.51249

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7818091/
https://www.ncbi.nlm.nih.gov/pubmed/33247623
http://dx.doi.org/10.1002/acn3.51249

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