Search Results - "Hobdy, Kierra P"

Patients with sporadic FTLD exhibit similar increases in lysosomal proteins and storage material as patients with FTD due to GRN mutations by Davis, Skylar E, Cook, Anna K, Hall, Justin A, Voskobiynyk, Yuliya, Carullo, Nancy V, Boyle, Nicholas R, Hakim, Ahmad R, Anderson, Kristian M, Hobdy, Kierra P, Pugh, Derian A, Murchison, Charles F, McMeekin, Laura J, Simmons, Micah, Margolies, Katherine A, Cowell, Rita M, Nana, Alissa L, Spina, Salvatore, Grinberg, Lea T, Miller, Bruce L, Seeley, William W, Arrant, Andrew E

“…Loss of function progranulin (GRN) mutations are a major autosomal dominant cause of frontotemporal dementia (FTD). Patients with FTD due to GRN mutations…”
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Similar lysosomal abnormalities in cortex of patients with sporadic FTLD‐TDP type A and patients with FTD‐GRN by Davis, Skylar E., Cook, Anna K., Voskobiynyk, Yuliya, Carullo, Nancy VN, Hakim, Ahmad R., Anderson, Kristian M., Hobdy, Kierra P., Pugh, Derian A, Murchison, Charles F, McMeekin, Laura J., Simmons, Micah S., Cowell, Rita M., Li, Alissa Nana, Spina, Salvatore, Grinberg, Lea Tenenholz, Miller, Bruce L., Seeley, William W., Arrant, Andrew E.

“…Background Loss‐of‐function mutations in progranulin (GRN) are an autosomal dominant cause of frontotemporal dementia (FTD). Progranulin is critical for…”
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