171 related articles for article (PubMed ID: 16897084)
1. The A431E mutation in PSEN1 causing familial Alzheimer's disease originating in Jalisco State, Mexico: an additional fifteen families.
Murrell J; Ghetti B; Cochran E; Macias-Islas MA; Medina L; Varpetian A; Cummings JL; Mendez MF; Kawas C; Chui H; Ringman JM
Neurogenetics; 2006 Nov; 7(4):277-9. PubMed ID: 16897084
[TBL] [Abstract][Full Text] [Related]
2. Founder effect for the Ala431Glu mutation of the presenilin 1 gene causing early-onset Alzheimer's disease in Mexican families.
Yescas P; Huertas-Vazquez A; Villarreal-Molina MT; Rasmussen A; Tusié-Luna MT; López M; Canizales-Quinteros S; Alonso ME
Neurogenetics; 2006 Jul; 7(3):195-200. PubMed ID: 16628450
[TBL] [Abstract][Full Text] [Related]
3. Autosomal dominant early onset Alzheimer's disease in the Mexican state of Jalisco: High frequency of the mutation PSEN1 c.1292C>A and phenotypic profile of patients.
Dumois-Petersen S; Gallegos-Arreola MP; Magaña-Torres MT; Perea-Díaz FJ; Ringman JM; Figuera LE
Am J Med Genet C Semin Med Genet; 2020 Dec; 184(4):1023-1029. PubMed ID: 33274538
[TBL] [Abstract][Full Text] [Related]
4. Novel presenilin 1 mutation (Ile408Thr) in an Italian family with late-onset Alzheimer's disease.
Tedde A; Bartoli A; Piaceri I; Ferrara S; Bagnoli S; Serio A; Sorbi S; Nacmias B
Neurosci Lett; 2016 Jan; 610():150-3. PubMed ID: 26549787
[TBL] [Abstract][Full Text] [Related]
5. The R269H mutation in presenilin-1 presenting as late-onset autosomal dominant Alzheimer's disease.
Larner AJ; Ray PS; Doran M
J Neurol Sci; 2007 Jan; 252(2):173-6. PubMed ID: 17188713
[TBL] [Abstract][Full Text] [Related]
6. Loss of stability and hydrophobicity of presenilin 1 mutations causing Alzheimer's disease.
Somavarapu AK; Kepp KP
J Neurochem; 2016 Apr; 137(1):101-11. PubMed ID: 26756738
[TBL] [Abstract][Full Text] [Related]
7. Novel presenilin 1 mutation (p.I83T) in Tunisian family with early-onset Alzheimer's disease.
Achouri-Rassas A; Ben Ali N; Fray S; Hadj Fredj S; Kechaou M; Zakraoui NO; Cherif A; Chabbi S; Anane N; Messaoud T; Gouider R; Belal S
Neurobiol Aging; 2015 Oct; 36(10):2904.e9-11. PubMed ID: 26145164
[TBL] [Abstract][Full Text] [Related]
8. Molecular diagnosis of autosomal dominant early onset Alzheimer's disease: an update.
Raux G; Guyant-Maréchal L; Martin C; Bou J; Penet C; Brice A; Hannequin D; Frebourg T; Campion D
J Med Genet; 2005 Oct; 42(10):793-5. PubMed ID: 16033913
[TBL] [Abstract][Full Text] [Related]
9. Presenilin 1 gene mutation (M139I) in a patient with an early-onset Alzheimer's disease: clinical characteristics and genetic identification.
Kim HJ; Kim HY; Ki CS; Kim SH
Neurol Sci; 2010 Dec; 31(6):781-3. PubMed ID: 20213228
[TBL] [Abstract][Full Text] [Related]
10. A novel PSEN1 gene mutation (L235R) associated with familial early-onset Alzheimer's disease.
Antonell A; Balasa M; Oliva R; Lladó A; Bosch B; Fabregat N; Fortea J; Molinuevo JL; Sánchez-Valle R
Neurosci Lett; 2011 May; 496(1):40-2. PubMed ID: 21501661
[TBL] [Abstract][Full Text] [Related]
11. A novel presenilin 1 mutation (Ser169del) in a Chinese family with early-onset Alzheimer's disease.
Guo J; Wei J; Liao S; Wang L; Jiang H; Tang B
Neurosci Lett; 2010 Jan; 468(1):34-7. PubMed ID: 19853643
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Clinical and genetic analysis of a Chilean family with early-onset autosomal dominant Alzheimer's disease.
Sinning M; van Rooyen JP; Venegas-Francke P; Vásquez C; Behrens MI; Ramírez A
J Alzheimers Dis; 2010; 21(3):757-61. PubMed ID: 20571222
[TBL] [Abstract][Full Text] [Related]
14.
Bagyinszky E; Lee HM; Van Giau V; Koh SB; Jeong JH; An SSA; Kim S
Int J Mol Sci; 2018 Sep; 19(9):. PubMed ID: 30200536
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Three novel presenilin 1 mutations marking the wide spectrum of age at onset and clinical patterns in familial Alzheimer's disease.
Roeber S; Müller-Sarnowski F; Kress J; Edbauer D; Kuhlmann T; Tüttelmann F; Schindler C; Winter P; Arzberger T; Müller U; Danek A; Kretzschmar HA
J Neural Transm (Vienna); 2015 Dec; 122(12):1715-9. PubMed ID: 26350633
[TBL] [Abstract][Full Text] [Related]
17. E280A PS-1 mutation causes Alzheimer's disease but age of onset is not modified by ApoE alleles.
Lendon CL; Martinez A; Behrens IM; Kosik KS; Madrigal L; Norton J; Neuman R; Myers A; Busfield F; Wragg M; Arcos M; Arango Viana JC; Ossa J; Ruiz A; Goate AM; Lopera F
Hum Mutat; 1997; 10(3):186-95. PubMed ID: 9298817
[TBL] [Abstract][Full Text] [Related]
18. Clinical and molecular studies reveal a PSEN1 mutation (L153V) in a Peruvian family with early-onset Alzheimer's disease.
Cornejo-Olivas MR; Yu CE; Mazzetti P; Mata IF; Meza M; Lindo-Samanamud S; Leverenz JB; Bird TD
Neurosci Lett; 2014 Mar; 563():140-3. PubMed ID: 24495933
[TBL] [Abstract][Full Text] [Related]
19. Homozygosity for the A431E mutation in PSEN1 presenting with a relatively aggressive phenotype.
Parker J; Mozaffar T; Messmore A; Deignan JL; Kimonis VE; Ringman JM
Neurosci Lett; 2019 Apr; 699():195-198. PubMed ID: 30716424
[TBL] [Abstract][Full Text] [Related]
20. Clinical phenotype of G206D mutation in the presenilin 1 gene in pathologically confirmed familial Alzheimer's disease.
Wu YY; Cheng IH; Lee CC; Chiu MJ; Lee MJ; Chen TF; Hsu JL
J Alzheimers Dis; 2011; 25(1):145-50. PubMed ID: 21335660
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]