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Prion protein codon 129 polymorphism and risk of Alzheimer disease.
Riemenschneider M, Klopp N, Xiang W, Wagenpfeil S, Vollmert C, Müller U, Förstl H, Illig T, Kretzschmar H, Kurz A. Riemenschneider M, et al. Among authors: kretzschmar h. Neurology. 2004 Jul 27;63(2):364-6. doi: 10.1212/01.wnl.0000130198.72589.69. Neurology. 2004. PMID: 15277640
Rare variants in β-Amyloid precursor protein (APP) and Parkinson's disease.
Schulte EC, Fukumori A, Mollenhauer B, Hor H, Arzberger T, Perneczky R, Kurz A, Diehl-Schmid J, Hüll M, Lichtner P, Eckstein G, Zimprich A, Haubenberger D, Pirker W, Brücke T, Bereznai B, Molnar MJ, Lorenzo-Betancor O, Pastor P, Peters A, Gieger C, Estivill X, Meitinger T, Kretzschmar HA, Trenkwalder C, Haass C, Winkelmann J. Schulte EC, et al. Among authors: kretzschmar ha. Eur J Hum Genet. 2015 Oct;23(10):1328-33. doi: 10.1038/ejhg.2014.300. Epub 2015 Jan 21. Eur J Hum Genet. 2015. PMID: 25604855 Free PMC article.
Novel PS1 mutation in a Bavarian kindred with familial Alzheimer disease.
Klünemann HH, Rogaeva E, Neumann M, Kretzschmar HA, Kandel M, Toulina A, Sato C, Salehi-Rad S, Pfister K, Klein HE, St George-Hyslop PH. Klünemann HH, et al. Among authors: kretzschmar ha. Alzheimer Dis Assoc Disord. 2004 Oct-Dec;18(4):256-8. Alzheimer Dis Assoc Disord. 2004. PMID: 15592140
Clinical features of rapidly progressive Alzheimer's disease.
Schmidt C, Redyk K, Meissner B, Krack L, von Ahsen N, Roeber S, Kretzschmar H, Zerr I. Schmidt C, et al. Among authors: kretzschmar h. Dement Geriatr Cogn Disord. 2010;29(4):371-8. doi: 10.1159/000278692. Epub 2010 May 5. Dement Geriatr Cogn Disord. 2010. PMID: 20453509 Free article.
500 results