These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
5. [From gene to disease; presenilins and Alzheimer disease]. Roos RA; Cruts M Ned Tijdschr Geneeskd; 2001 Oct; 145(42):2027-9. PubMed ID: 11695101 [TBL] [Abstract][Full Text] [Related]
6. A novel missense mutation (G209R) in exon 8 of the presenilin 1 gene in a Japanese family with presenile familial Alzheimer's disease. Mutation in brief no. 254. Online. Sugiyama N; Suzuki K; Matsumura T; Kawanishi C; Onishi H; Yamada Y; Iseki E; Kosaka K Hum Mutat; 1999; 14(1):90. PubMed ID: 10447269 [TBL] [Abstract][Full Text] [Related]
7. Novel presenilin 1 mutation (S170F) causing Alzheimer disease with Lewy bodies in the third decade of life. Snider BJ; Norton J; Coats MA; Chakraverty S; Hou CE; Jervis R; Lendon CL; Goate AM; McKeel DW; Morris JC Arch Neurol; 2005 Dec; 62(12):1821-30. PubMed ID: 16344340 [TBL] [Abstract][Full Text] [Related]
8. Alzheimer's disease. Missense on the membrane. Selkoe DJ Nature; 1995 Jun; 375(6534):734-5. PubMed ID: 7596402 [No Abstract] [Full Text] [Related]
9. Amyloid angiopathy in a Volga German family with Alzheimer's disease and a presenilin-2 mutation (N141I). Nochlin D; Bird TD; Nemens EJ; Ball MJ; Sumi SM Ann Neurol; 1998 Jan; 43(1):131-5. PubMed ID: 9450781 [TBL] [Abstract][Full Text] [Related]
10. Dementia, pyramidal system involvement, and leukoencephalopathy with a presenilin 1 mutation. Marrosu MG; Floris G; Costa G; Schirru L; Spinicci G; Cherchi MV; Mura M; Mascia MG; Cocco E Neurology; 2006 Jan; 66(1):108-11. PubMed ID: 16401857 [TBL] [Abstract][Full Text] [Related]
11. A novel presenilin 1 mutation (Y154N) in a patient with early onset Alzheimer's disease with spastic paraparesis. Hattori S; Sakuma K; Wakutani Y; Wada K; Shimoda M; Urakami K; Kowa H; Nakashima K Neurosci Lett; 2004 Sep; 368(3):319-22. PubMed ID: 15364419 [TBL] [Abstract][Full Text] [Related]
12. [Image characterization of Alzheimer's disease associated with the E280A-PS1 mutation. Case-control study: MRI findings]. Lopera F; Tobón N; Arcos-Burgos M; Vargas S; Gutiérrez JE; Rosselli M; Ardila A Rev Neurol; 1999 Jul 1-15; 29(1):6-12. PubMed ID: 10528301 [TBL] [Abstract][Full Text] [Related]
13. Presenilin 1 Glu318Gly polymorphism: interpret with caution. Goldman JS; Johnson JK; McElligott K; Suchowersky O; Miller BL; Van Deerlin VM Arch Neurol; 2005 Oct; 62(10):1624-7. PubMed ID: 16216949 [TBL] [Abstract][Full Text] [Related]
14. A mutant PSEN1 causes dementia with Lewy bodies and variant Alzheimer's disease. Ishikawa A; Piao YS; Miyashita A; Kuwano R; Onodera O; Ohtake H; Suzuki M; Nishizawa M; Takahashi H Ann Neurol; 2005 Mar; 57(3):429-34. PubMed ID: 15732120 [TBL] [Abstract][Full Text] [Related]
15. Missense mutations in the chromosome 14 familial Alzheimer's disease presenilin 1 gene. Poorkaj P; Sharma V; Anderson L; Nemens E; Alonso ME; Orr H; White J; Heston L; Bird TD; Schellenberg GD Hum Mutat; 1998; 11(3):216-21. PubMed ID: 9521423 [TBL] [Abstract][Full Text] [Related]
16. Prominent behavioural and psychiatric symptoms in early-onset Alzheimer's disease in a sib pair with the presenilin-1 gene R269G mutation. Doran M; Larner AJ Eur Arch Psychiatry Clin Neurosci; 2004 Jun; 254(3):187-9. PubMed ID: 15205973 [TBL] [Abstract][Full Text] [Related]
17. [Alzheimer's disease and genetic factors]. Leuba G; Savioz A Rev Med Suisse Romande; 1997 Nov; 117(11):871-8. PubMed ID: 9471651 [No Abstract] [Full Text] [Related]
18. S182 and STM2 gene missense mutations in sporadic Alzheimer disease. Higuchi S; Matsushita S; Hasegawa Y; Muramatsu T; Itabashi S; Arai H Am J Med Genet; 1996 Jul; 67(4):429. PubMed ID: 8837717 [No Abstract] [Full Text] [Related]
20. Tau is central in the genetic Alzheimer-frontotemporal dementia spectrum. Dermaut B; Kumar-Singh S; Rademakers R; Theuns J; Cruts M; Van Broeckhoven C Trends Genet; 2005 Dec; 21(12):664-72. PubMed ID: 16221505 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]