Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Hemorrhage and APP[original query] |
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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 |
Screening for familial APP mutations in sporadic cerebral amyloid angiopathy. PloS one 2010 5 (11): e13949. Biffi Alessandro, Plourde Anna, Shen Yiping, Onofrio Robert, Smith Eric E, Frosch Matthew, Prada Claudia M, Gusella James, Greenberg Steven M, Rosand Jonath |
No evidence of APP point mutation and locus duplication in individuals with cerebral amyloid angiopathy. European journal of neurology : the official journal of the European Federation of Neurological Societies 2011 Oct 18 (10): 1279-81. Domingues-Montanari S, Parés M, Hernández-Guillamon M, Fernández-Cadenas I, Mendioroz M, Ortega G, Boada M, Masjuan J, Huertas N, Alvarez-Sabín J, Delgado P, Montaner J, |
Mutation in the 3'untranslated region of APP as a genetic determinant of cerebral amyloid angiopathy. European journal of human genetics : EJHG 2015 Apr . Nicolas Gaël, Wallon David, Goupil Claudia, Richard Anne-Claire, Pottier Cyril, Dorval Véronique, Sarov-Rivière Mariana, Riant Florence, Hervé Dominique, Amouyel Philippe, Guerchet Maelenn, Ndamba-Bandzouzi Bebene, Mbelesso Pascal, Dartigues Jean-François, Lambert Jean-Charles, Preux Pierre-Marie, Frebourg Thierry, Campion Dominique, Hannequin Didier, Tournier-Lasserve Elisabeth, Hébert Sébastien S, Rovelet-Lecrux An |
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