Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Headache and APP[original query] |
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Increased prevalence of significant recurrent headache in preclinical familial Alzheimer's disease mutation carriers. Dementia and geriatric cognitive disorders 2008 25 (4): 380-4. Ringman John M, Romano Joseph D, Medina Luis D, Rodriguez-Agudelo Yaneth, Schaffer Barbara, Varpetian Arousiak, Ortiz Freddy, Fitten L Jamie, Cummings Jeffrey L, Baloh Robert |
Hereditary cerebral hemorrhage with amyloidosis associated with the E693K mutation of APP. Archives of neurology 2010 Aug 67 (8): 987-95. Bugiani Orso, Giaccone Giorgio, Rossi Giacomina, Mangieri Michela, Capobianco Raffaella, Morbin Michela, Mazzoleni Giulia, Cupidi Chiara, Marcon Gabriella, Giovagnoli Annarita, Bizzi Alberto, Di Fede Giuseppe, Puoti Gianfranco, Carella Francesco, Salmaggi Andrea, Romorini Alessandro, Patruno Giorgio M, Magoni Mauro, Padovani Alessandro, Tagliavini Fabriz |
Cerebral amyloid angiopathy-related inflammation: a case report presenting with a rare variant in SORL1 gene. BMC neurology 2019 5 19 (1): 97. Du Yanjiao, Liu Chao, Ma Congmin, Xu Xiaohui, Zhou Xufeng, Zhou Haitao, Huang Ch |
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- Page last updated:May 22, 2023
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