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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Oct 2, 2023. (Total: 221654Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Amyloidosis and APP[original query]
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
APP mutations in the Aß coding region are associated with abundant cerebral deposition of Aß38.
Acta neuropathologica 2012 Dec 124 (6): 809-21.
Moro Maria Luisa, Giaccone Giorgio, Lombardi Raffaella, Indaco Antonio, Uggetti Andrea, Morbin Michela, Saccucci Stefania, Di Fede Giuseppe, Catania Marcella, Walsh Dominic M, Demarchi Andrea, Rozemuller Annemieke, Bogdanovic Nenad, Bugiani Orso, Ghetti Bernardino, Tagliavini Fabriz
Impact of cerebrospinal fluid matrix on the detection of Alzheimer's disease with Aß42 and influence of disease on the total-Aß42/Aß40 ratio.
Journal of neurochemistry 2015 Sep .
Slemmon J Randall, Shapiro Alice, Mercken Marc, Streffer Johannes, Romano Gary, Andreasen Niels, Zetterberg Henrik, Blennow K
A Young Man with Cognitive Impairment and a Heart Condition.
Journal of Alzheimer's disease : JAD 2022 7 89 (2): 405-410.
Russo Mirella, Santilli Matteo, De Rosa Matteo A, Calisi Dario, Dono Fedele, Mattoli Maria Vittoria, Bonanni Laura, Onofrj Marco, Sensi Stefano
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