170 related articles for article (PubMed ID: 30599314)
1. Genetic influences on white matter and metabolism abnormal change in Alzheimer's disease: Meta-analysis for neuroimaging research on presenilin 1 mutation.
Gu X; Chu T; Liu L; Han X
Clin Neurol Neurosurg; 2019 Feb; 177():47-53. PubMed ID: 30599314
[TBL] [Abstract][Full Text] [Related]
2. Presenilin-1 mutation is associated with a hippocampus defect in alzheimer's disease: Meta-Analysis for neuroimaging research.
Gu X; Zhao M; Han X; Liu L
Clin Neurol Neurosurg; 2020 Apr; 191():105679. PubMed ID: 32004985
[TBL] [Abstract][Full Text] [Related]
3. White Matter Abnormalities Track Disease Progression in PSEN1 Autosomal Dominant Alzheimer's Disease.
Sánchez-Valle R; Monté GC; Sala-Llonch R; Bosch B; Fortea J; Lladó A; Antonell A; Balasa M; Bargalló N; Molinuevo JL
J Alzheimers Dis; 2016; 51(3):827-35. PubMed ID: 26923015
[TBL] [Abstract][Full Text] [Related]
4. Challenges in diffusion MRI meta-analysis: A discussion of "Genetic influences on white matter and metabolism abnormal change in Alzheimer's disease: Meta-analysis for neuroimaging research on presenilin 1 mutation".
Benkert H; Bhatia S; Mirza-Davies A; Tan ZX; Harrison JR
Clin Neurol Neurosurg; 2020 Dec; 199():106279. PubMed ID: 33091654
[No Abstract] [Full Text] [Related]
5. Genetic determinants of white matter hyperintensities and amyloid angiopathy in familial Alzheimer's disease.
Ryan NS; Biessels GJ; Kim L; Nicholas JM; Barber PA; Walsh P; Gami P; Morris HR; Bastos-Leite AJ; Schott JM; Beck J; Mead S; Chavez-Gutierrez L; de Strooper B; Rossor MN; Revesz T; Lashley T; Fox NC
Neurobiol Aging; 2015 Dec; 36(12):3140-3151. PubMed ID: 26410308
[TBL] [Abstract][Full Text] [Related]
6. APOE genotype and neuroimaging markers of Alzheimer's disease: systematic review and meta-analysis.
Liu Y; Yu JT; Wang HF; Han PR; Tan CC; Wang C; Meng XF; Risacher SL; Saykin AJ; Tan L
J Neurol Neurosurg Psychiatry; 2015 Feb; 86(2):127-34. PubMed ID: 24838911
[TBL] [Abstract][Full Text] [Related]
7. Genetic influences on atrophy patterns in familial Alzheimer's disease: a comparison of APP and PSEN1 mutations.
Scahill RI; Ridgway GR; Bartlett JW; Barnes J; Ryan NS; Mead S; Beck J; Clarkson MJ; Crutch SJ; Schott JM; Ourselin S; Warren JD; Hardy J; Rossor MN; Fox NC
J Alzheimers Dis; 2013; 35(1):199-212. PubMed ID: 23380992
[TBL] [Abstract][Full Text] [Related]
8. Widespread white matter and conduction defects in PSEN1-related spastic paraparesis.
Soosman SK; Joseph-Mathurin N; Braskie MN; Bordelon YM; Wharton D; Casado M; Coppola G; McCallum H; Nuwer M; Coutin-Churchman P; Apostolova LG; Benzinger T; Ringman JM
Neurobiol Aging; 2016 Nov; 47():201-209. PubMed ID: 27614114
[TBL] [Abstract][Full Text] [Related]
9. Clinical, imaging, pathological, and biochemical characterization of a novel presenilin 1 mutation (N135Y) causing Alzheimer's disease.
Natelson Love M; Clark DG; Cochran JN; Den Beste KA; Geldmacher DS; Benzinger TL; Gordon BA; Morris JC; Bateman RJ; Roberson ED
Neurobiol Aging; 2017 Jan; 49():216.e7-216.e13. PubMed ID: 27793474
[TBL] [Abstract][Full Text] [Related]
10. Clinical characterization of a presenilin 1 mutation (F177S) in a family with very early-onset Alzheimer's disease in the third decade of life.
Hausner L; Tschäpe JA; Schmitt HP; Hentschel F; Hartmann T; Frölich L
Alzheimers Dement; 2014 Mar; 10(2):e27-39. PubMed ID: 23850332
[TBL] [Abstract][Full Text] [Related]
11. Increased cortical thickness and caudate volume precede atrophy in PSEN1 mutation carriers.
Fortea J; Sala-Llonch R; Bartrés-Faz D; Bosch B; Lladó A; Bargalló N; Molinuevo JL; Sánchez-Valle R
J Alzheimers Dis; 2010; 22(3):909-22. PubMed ID: 20858974
[TBL] [Abstract][Full Text] [Related]
12. Identification of a Pathogenic PSEN1 Ala285Val Mutation Associated with Early-Onset Alzheimer's Disease.
Vo VG; Pyun JM; Bagyinszky E; An SSA; Kim SY
Curr Alzheimer Res; 2020; 17(5):438-445. PubMed ID: 32589559
[TBL] [Abstract][Full Text] [Related]
13. White matter hyperintensities and patterns of atrophy in early onset Alzheimer's disease with causative gene mutations.
Mao C; Li J; Huang X; Dong L; Liu C; Peng B; Cui L; Gao J
Clin Neurol Neurosurg; 2021 Apr; 203():106552. PubMed ID: 33601235
[TBL] [Abstract][Full Text] [Related]
14. Cognition-related white matter integrity dysfunction in Alzheimer's disease with diffusion tensor image.
Li Y; Feng F; Lin P; Huang ZG; Liu T; Zhou B; Yao H; Zheng L; Li C; Wang P; Zhang Z; Guo Y; Wang L; An N; Zhu X; Zhang X; Wang J
Brain Res Bull; 2018 Oct; 143():207-216. PubMed ID: 30240840
[TBL] [Abstract][Full Text] [Related]
15. Integration of bioinformatics and imaging informatics for identifying rare PSEN1 variants in Alzheimer's disease.
Nho K; Horgusluoglu E; Kim S; Risacher SL; Kim D; Foroud T; Aisen PS; Petersen RC; Jack CR; Shaw LM; Trojanowski JQ; Weiner MW; Green RC; Toga AW; Saykin AJ;
BMC Med Genomics; 2016 Aug; 9 Suppl 1(Suppl 1):30. PubMed ID: 27535542
[TBL] [Abstract][Full Text] [Related]
16. Mutational analysis in familial Alzheimer's disease of Han Chinese in Taiwan with a predominant mutation PSEN1 p.Met146Ile.
Lin YS; Cheng CY; Liao YC; Hong CJ; Fuh JL
Sci Rep; 2020 Nov; 10(1):19769. PubMed ID: 33188256
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Association Between Amyloid and Tau Accumulation in Young Adults With Autosomal Dominant Alzheimer Disease.
Quiroz YT; Sperling RA; Norton DJ; Baena A; Arboleda-Velasquez JF; Cosio D; Schultz A; Lapoint M; Guzman-Velez E; Miller JB; Kim LA; Chen K; Tariot PN; Lopera F; Reiman EM; Johnson KA
JAMA Neurol; 2018 May; 75(5):548-556. PubMed ID: 29435558
[TBL] [Abstract][Full Text] [Related]
19. Presenilin-1 mutation position influences amyloidosis, small vessel disease, and dementia with disease stage.
Joseph-Mathurin N; Feldman RL; Lu R; Shirzadi Z; Toomer C; Saint Clair JR; Ma Y; McKay NS; Strain JF; Kilgore C; Friedrichsen KA; Chen CD; Gordon BA; Chen G; Hornbeck RC; Massoumzadeh P; McCullough AA; Wang Q; Li Y; Wang G; Keefe SJ; Schultz SA; Cruchaga C; Preboske GM; Jack CR; Llibre-Guerra JJ; Allegri RF; Ances BM; Berman SB; Brooks WS; Cash DM; Day GS; Fox NC; Fulham M; Ghetti B; Johnson KA; Jucker M; Klunk WE; la Fougère C; Levin J; Niimi Y; Oh H; Perrin RJ; Reischl G; Ringman JM; Saykin AJ; Schofield PR; Su Y; Supnet-Bell C; Vöglein J; Yakushev I; Brickman AM; Morris JC; McDade E; Xiong C; Bateman RJ; Chhatwal JP; Benzinger TLS;
Alzheimers Dement; 2024 Apr; 20(4):2680-2697. PubMed ID: 38380882
[TBL] [Abstract][Full Text] [Related]
20. A Novel PSEN1 M139L Mutation Found in a Chinese Pedigree with Early-Onset Alzheimer's Disease Increases Aβ42/Aβ40 ratio.
Qiu Q; Shen L; Jia L; Wang Q; Li F; Li Y; Jia J
J Alzheimers Dis; 2019; 69(1):199-212. PubMed ID: 30958370
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
