117 related articles for article (PubMed ID: 18833506)
1. [Familial Alzheimer's disease with presenilin 2 N141I mutation. A case report].
Nikisch G; Wiedemann G; Kiessling B; Hertel A
Fortschr Neurol Psychiatr; 2008 Oct; 76(10):606-9. PubMed ID: 18833506
[TBL] [Abstract][Full Text] [Related]
2. Three-year follow-up of a patient with early-onset Alzheimer's disease with presenilin-2 N141I mutation - case report and review of the literature.
Nikisch G; Hertel A; Kiessling B; Wagner T; Krasz D; Hofmann E; Wiedemann G
Eur J Med Res; 2008 Dec; 13(12):579-84. PubMed ID: 19073399
[TBL] [Abstract][Full Text] [Related]
3. Evaluation of therapeutic response to donepezil by positron emission tomography.
Shimada A; Hashimoto H; Kawabe J; Higashiyama S; Kai T; Kataoka K; Tagawa R; Kawarada Y; Nakanishi A; Inoue K; Shiomi S; Kiriike N
Osaka City Med J; 2011 Jun; 57(1):11-9. PubMed ID: 22106763
[TBL] [Abstract][Full Text] [Related]
4. Identification of PSEN2 mutation p.N141I in Argentine pedigrees with early-onset familial Alzheimer's disease.
Muchnik C; Olivar N; Dalmasso MC; Azurmendi PJ; Liberczuk C; Morelli L; Brusco LI
Neurobiol Aging; 2015 Oct; 36(10):2674-7.e1. PubMed ID: 26166204
[TBL] [Abstract][Full Text] [Related]
5. Generation of gene edited hiPSC from familial Alzheimer's disease patient carrying N141I missense mutation in presenilin 2.
Marei HE; Althani A; Afifi N; Hasan A; Caceci T; Pozzoli G; Cenciarelli C
Stem Cell Res; 2021 Oct; 56():102552. PubMed ID: 34634760
[TBL] [Abstract][Full Text] [Related]
6. Mutational analysis in early-onset familial Alzheimer's disease in Mainland China.
Jiao B; Tang B; Liu X; Xu J; Wang Y; Zhou L; Zhang F; Yan X; Zhou Y; Shen L
Neurobiol Aging; 2014 Aug; 35(8):1957.e1-6. PubMed ID: 24650794
[TBL] [Abstract][Full Text] [Related]
7. Time course of glucose metabolism in relation to cognitive performance and postmortem neuropathology in Met146Val PSEN1 mutation carriers.
Schöll M; Almkvist O; Bogdanovic N; Wall A; Långström B; Viitanen M; Nordberg A
J Alzheimers Dis; 2011; 24(3):495-506. PubMed ID: 21297272
[TBL] [Abstract][Full Text] [Related]
8. Probable Novel APP Met671Leu Mutation in a Chinese Han Family with Early-Onset Alzheimer's Disease.
Ma L; Wang F; Chen S; Wang S; Wang Z; Xia M; Li Y; Ma H; Shang J; Zhang J
Neuromolecular Med; 2024 Mar; 26(1):6. PubMed ID: 38504005
[TBL] [Abstract][Full Text] [Related]
9. Clinical and neuroimaging characterization of Chinese dementia patients with PSEN1 and PSEN2 mutations.
Shi Z; Wang Y; Liu S; Liu M; Liu S; Zhou Y; Wang J; Cai L; Huo YR; Gao S; Ji Y
Dement Geriatr Cogn Disord; 2015; 39(1-2):32-40. PubMed ID: 25323700
[TBL] [Abstract][Full Text] [Related]
10. Early-onset Alzheimer's disease due to mutations of the presenilin-1 gene on chromosome 14: a 7-year follow-up of a patient with a mutation at codon 139.
Hüll M; Fiebich BL; Dykierek P; Schmidtke K; Nitzsche E; Orszagh M; Deuschl G; Moser E; Schumacher M; Lücking C; Berger M; Bauer J
Eur Arch Psychiatry Clin Neurosci; 1998; 248(3):123-9. PubMed ID: 9728730
[TBL] [Abstract][Full Text] [Related]
11. Two-year follow-up of amyloid deposition in patients with Alzheimer's disease.
Engler H; Forsberg A; Almkvist O; Blomquist G; Larsson E; Savitcheva I; Wall A; Ringheim A; Långström B; Nordberg A
Brain; 2006 Nov; 129(Pt 11):2856-66. PubMed ID: 16854944
[TBL] [Abstract][Full Text] [Related]
12. Alzheimer's disease phenotypes and genotypes associated with mutations in presenilin 2.
Jayadev S; Leverenz JB; Steinbart E; Stahl J; Klunk W; Yu CE; Bird TD
Brain; 2010 Apr; 133(Pt 4):1143-54. PubMed ID: 20375137
[TBL] [Abstract][Full Text] [Related]
13. A novel mutation in the PSEN2 gene (T430M) associated with variable expression in a family with early-onset Alzheimer disease.
Ezquerra M; Lleó A; Castellví M; Queralt R; Santacruz P; Pastor P; Molinuevo JL; Blesa R; Oliva R
Arch Neurol; 2003 Aug; 60(8):1149-51. PubMed ID: 12925374
[TBL] [Abstract][Full Text] [Related]
14. A pathogenic
Giau VV; Pyun JM; Bagyinszky E; An SSA; Kim S
Clin Interv Aging; 2018; 13():1321-1329. PubMed ID: 30104866
[TBL] [Abstract][Full Text] [Related]
15. Brain 18 F-Florbetapir PET/CT Findings in an Early-onset Alzheimer Disease Patient Carrying Presenilin-1 G378E Mutation.
Cistaro A; Quartuccio N; Cassalia L; Vai D; Guerra UP; Atzori C; Rainero I; Imperiale D
Alzheimer Dis Assoc Disord; 2022 Oct-Dec 01; 36(4):347-349. PubMed ID: 34132671
[TBL] [Abstract][Full Text] [Related]
16. Novel presenilin mutations within Moroccan patients with Early-Onset Alzheimer's Disease.
El Kadmiri N; Zaid N; Zaid Y; Tadevosyan A; Hachem A; Dubé MP; Hamzi K; El Moutawakil B; Slassi I; Nadifi S
Neuroscience; 2014 Jun; 269():215-22. PubMed ID: 24704512
[TBL] [Abstract][Full Text] [Related]
17. Early-Onset Familial Alzheimer Disease Variant PSEN2 N141I Heterozygosity is Associated with Altered Microglia Phenotype.
Fung S; Smith CL; Prater KE; Case A; Green K; Osnis L; Winston C; Kinoshita Y; Sopher B; Morrison RS; Garden GA; Jayadev S
J Alzheimers Dis; 2020; 77(2):675-688. PubMed ID: 32741831
[TBL] [Abstract][Full Text] [Related]
18. The novel I213S mutation in PSEN1 gene is located in a hotspot codon associated with familial early-onset Alzheimer's disease.
Catania M; Marti A; Rossi G; Fioretti A; Boiocchi C; Ricci M; Gasparini F; Beltrami D; Crepaldi V; Redaelli V; Giaccone G; Di Fede G
Neurobiol Aging; 2022 Apr; 112():191-196. PubMed ID: 35231845
[TBL] [Abstract][Full Text] [Related]
19. Pilot whole-exome sequencing of a German early-onset Alzheimer's disease cohort reveals a substantial frequency of PSEN2 variants.
Blauwendraat C; Wilke C; Jansen IE; Schulte C; Simón-Sánchez J; Metzger FG; Bender B; Gasser T; Maetzler W; Rizzu P; Heutink P; Synofzik M
Neurobiol Aging; 2016 Jan; 37():208.e11-208.e17. PubMed ID: 26522186
[TBL] [Abstract][Full Text] [Related]
20. A novel mutation in the predicted TMIII domain of the PSEN2 gene in an Italian pedigree with atypical Alzheimer's disease.
Piscopo P; Talarico G; Crestini A; Gasparini M; Malvezzi-Campeggi L; Piacentini E; Lenzi GL; Bruno G; Confaloni A
J Alzheimers Dis; 2010; 20(1):43-7. PubMed ID: 20164579
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]