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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 4, 2023. (Total: 223640Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Aphasia and TREM2[original query]
Heterozygous TREM2 mutations in frontotemporal dementia.
Neurobiology of aging 2014 Apr 35 (4): 934.e7-10.
Borroni Barbara, Ferrari Francesca, Galimberti Daniela, Nacmias Benedetta, Barone Cinzia, Bagnoli Silvia, Fenoglio Chiara, Piaceri Irene, Archetti Silvana, Bonvicini Cristian, Gennarelli Massimo, Turla Marinella, Scarpini Elio, Sorbi Sandro, Padovani Alessand
Genetic screen in a large series of patients with primary progressive aphasia.
Alzheimer's & dementia : the journal of the Alzheimer's Association 2019 1 15 (4): 553-560.
Ramos Eliana Marisa, Dokuru Deepika Reddy, Van Berlo Victoria, Wojta Kevin, Wang Qing, Huang Alden Y, Miller Zachary A, Karydas Anna M, Bigio Eileen H, Rogalski Emily, Weintraub Sandra, Rader Benjamin, Miller Bruce L, Gorno-Tempini Maria Luisa, Mesulam Marek-Marsel, Coppola Giovan
C9orf72 expansions are the most common cause of genetic frontotemporal dementia in a Southeast Asian cohort.
Annals of clinical and translational neurology 2023 2 .
Tan Yi Jayne, Yong Alisa C W, Foo Jia Nee, Lian Michelle M, Lim Weng Khong, Dominguez Jacqueline, Fong Zhi Hui, Narasimhalu Kaavya, Chiew Hui Jin, Ng Kok Pin, Ting Simon K S, Kandiah Nagaendran, Ng Adeline S
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