159 related articles for article (PubMed ID: 33274538)
1. 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]
2.
Giau VV; Bagyinszky E; Youn YC; An SSA; Kim S
Int J Mol Sci; 2019 Sep; 20(19):. PubMed ID: 31557888
[TBL] [Abstract][Full Text] [Related]
3. APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases.
Lanoiselée HM; Nicolas G; Wallon D; Rovelet-Lecrux A; Lacour M; Rousseau S; Richard AC; Pasquier F; Rollin-Sillaire A; Martinaud O; Quillard-Muraine M; de la Sayette V; Boutoleau-Bretonniere C; Etcharry-Bouyx F; Chauviré V; Sarazin M; le Ber I; Epelbaum S; Jonveaux T; Rouaud O; Ceccaldi M; Félician O; Godefroy O; Formaglio M; Croisile B; Auriacombe S; Chamard L; Vincent JL; Sauvée M; Marelli-Tosi C; Gabelle A; Ozsancak C; Pariente J; Paquet C; Hannequin D; Campion D;
PLoS Med; 2017 Mar; 14(3):e1002270. PubMed ID: 28350801
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. A genetic screen of the mutations in the Korean patients with early-onset Alzheimer's disease.
An SS; Park SA; Bagyinszky E; Bae SO; Kim YJ; Im JY; Park KW; Park KH; Kim EJ; Jeong JH; Kim JH; Han HJ; Choi SH; Kim S
Clin Interv Aging; 2016; 11():1817-1822. PubMed ID: 28008242
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Clinical phenotype and genetic associations in autosomal dominant familial Alzheimer's disease: a case series.
Ryan NS; Nicholas JM; Weston PSJ; Liang Y; Lashley T; Guerreiro R; Adamson G; Kenny J; Beck J; Chavez-Gutierrez L; de Strooper B; Revesz T; Holton J; Mead S; Rossor MN; Fox NC
Lancet Neurol; 2016 Dec; 15(13):1326-1335. PubMed ID: 27777022
[TBL] [Abstract][Full Text] [Related]
8.
Orozco-Barajas M; Oropeza-Ruvalcaba Y; Canales-Aguirre AA; Sánchez-González VJ
Front Aging Neurosci; 2022; 14():860529. PubMed ID: 35959289
[TBL] [Abstract][Full Text] [Related]
9. Potential Modifying Effect of the
Valdez-Gaxiola CA; Maciel-Cruz EJ; Hernández-Peña R; Dumois-Petersen S; Rosales-Leycegui F; Gallegos-Arreola MP; Moreno-Ortiz JM; Figuera LE
Int J Mol Sci; 2023 Oct; 24(21):. PubMed ID: 37958671
[TBL] [Abstract][Full Text] [Related]
10. Genetic screening in early-onset Alzheimer's disease identified three novel presenilin mutations.
Wong TH; Seelaar H; Melhem S; Rozemuller AJM; van Swieten JC
Neurobiol Aging; 2020 Feb; 86():201.e9-201.e14. PubMed ID: 30797548
[TBL] [Abstract][Full Text] [Related]
11. Early onset familial Alzheimer's disease: Mutation frequency in 31 families.
Janssen JC; Beck JA; Campbell TA; Dickinson A; Fox NC; Harvey RJ; Houlden H; Rossor MN; Collinge J
Neurology; 2003 Jan; 60(2):235-9. PubMed ID: 12552037
[TBL] [Abstract][Full Text] [Related]
12. Systematic genetic study of Alzheimer disease in Latin America: mutation frequencies of the amyloid beta precursor protein and presenilin genes in Colombia.
Arango D; Cruts M; Torres O; Backhovens H; Serrano ML; Villareal E; Montañes P; Matallana D; Cano C; Van Broeckhoven C; Jacquier M
Am J Med Genet; 2001 Oct; 103(2):138-43. PubMed ID: 11568920
[TBL] [Abstract][Full Text] [Related]
13. Discovery and validation of dominantly inherited Alzheimer's disease mutations in populations from Latin America.
Takada LT; Aláez-Verson C; Burgute BD; Nitrini R; Sosa AL; Castilhos RM; Chaves MF; Longoria EM; Carrillo-Sánchez K; Brucki SMD; Flores-Lagunes LL; Molina C; Olivares MJ; Ziegemeier E; Petranek J; Goate AM; Cruchaga C; Renton AE; Fernández MV; Day GS; McDade E; Bateman RJ; Karch CM; Llibre-Guerra JJ;
Alzheimers Res Ther; 2022 Aug; 14(1):108. PubMed ID: 35932032
[TBL] [Abstract][Full Text] [Related]
14. Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum.
Campion D; Dumanchin C; Hannequin D; Dubois B; Belliard S; Puel M; Thomas-Anterion C; Michon A; Martin C; Charbonnier F; Raux G; Camuzat A; Penet C; Mesnage V; Martinez M; Clerget-Darpoux F; Brice A; Frebourg T
Am J Hum Genet; 1999 Sep; 65(3):664-70. PubMed ID: 10441572
[TBL] [Abstract][Full Text] [Related]
15. Exome sequencing identifies 2 novel presenilin 1 mutations (p.L166V and p.S230R) in British early-onset Alzheimer's disease.
Sassi C; Guerreiro R; Gibbs R; Ding J; Lupton MK; Troakes C; Lunnon K; Al-Sarraj S; Brown KS; Medway C; Lord J; Turton J; Mann D; Snowden J; Neary D; Harris J; Bras J; ; Morgan K; Powell JF; Singleton A; Hardy J
Neurobiol Aging; 2014 Oct; 35(10):2422.e13-6. PubMed ID: 24880964
[TBL] [Abstract][Full Text] [Related]
16. Presenilin 1 and APP Gene Mutations in Early-Onset AD Families from a Southeast Region of China.
Zhou J; Chen Y; Meng F; Zhang K; Liu X; Peng G
Curr Alzheimer Res; 2020; 17(6):540-546. PubMed ID: 32579498
[TBL] [Abstract][Full Text] [Related]
17. Identification of the Third Case of PSEN1 Tyr389His Variant in Early-Onset Alzheimer's Disease in Korea.
Shim KH; Kang S; An SSA; Kang MJ
Int J Mol Sci; 2022 Dec; 23(24):. PubMed ID: 36555832
[TBL] [Abstract][Full Text] [Related]
18. The identification of PSEN1 p.Tyr159Ser mutation in a non-canonic early-onset Alzheimer's disease family.
Li H; Li Y; Liang W; Wei ZZ; Li X; Tian Y; Qiao S; Yang Y; Yang L; Wu D; Yin W; Liu H; Zhang W; Zhang Y; Wang Z
Mol Cell Neurosci; 2022 May; 120():103715. PubMed ID: 35247599
[TBL] [Abstract][Full Text] [Related]
19. Molecular Genetics of Early- and Late-Onset Alzheimer's Disease.
Uddin MS; Hasana S; Hossain MF; Islam MS; Behl T; Perveen A; Hafeez A; Ashraf GM
Curr Gene Ther; 2021; 21(1):43-52. PubMed ID: 33231156
[TBL] [Abstract][Full Text] [Related]
20. Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families.
Cruchaga C; Haller G; Chakraverty S; Mayo K; Vallania FL; Mitra RD; Faber K; Williamson J; Bird T; Diaz-Arrastia R; Foroud TM; Boeve BF; Graff-Radford NR; St Jean P; Lawson M; Ehm MG; Mayeux R; Goate AM;
PLoS One; 2012; 7(2):e31039. PubMed ID: 22312439
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
