140 related articles for article (PubMed ID: 36434476)
1. Genetic analysis of the LRP10 gene in Chinese patients with Parkinson's disease.
Song N; Wang Y; Zhou L; Zhang J; Wu F; Li M; Wang W; Liu Y; Lu X; Chen Q; Zhang N; Yan Y; Han F
Neurol Sci; 2023 Mar; 44(3):905-912. PubMed ID: 36434476
[TBL] [Abstract][Full Text] [Related]
2. Role of LRP10 in Parkinson's disease in a Taiwanese cohort.
Liao TW; Wang CC; Chung WH; Su SC; Chin SH; Fung HC; Wu YR
Parkinsonism Relat Disord; 2021 Aug; 89():79-83. PubMed ID: 34246039
[TBL] [Abstract][Full Text] [Related]
3. LRP10 in autosomal-dominant Parkinson's disease.
Chen Y; Cen Z; Zheng X; Pan Q; Chen X; Zhu L; Chen S; Wu H; Xie F; Wang H; Yang D; Wang L; Zhang B; Luo W
Mov Disord; 2019 Jun; 34(6):912-916. PubMed ID: 30964957
[TBL] [Abstract][Full Text] [Related]
4. LRP10 variants in Parkinson's disease and dementia with Lewy bodies in the South-West of the Netherlands.
Vergouw LJM; Ruitenberg A; Wong TH; Melhem S; Breedveld GJ; Criscuolo C; De Michele G; de Jong FJ; Bonifati V; van Swieten JC; Quadri M
Parkinsonism Relat Disord; 2019 Aug; 65():243-247. PubMed ID: 31147221
[TBL] [Abstract][Full Text] [Related]
5. Screening of LRP10 mutations in Parkinson's disease patients from Italy.
Manini A; Straniero L; Monfrini E; Percetti M; Vizziello M; Franco G; Rimoldi V; Zecchinelli A; Pezzoli G; Corti S; Comi GP; Duga S; Di Fonzo A
Parkinsonism Relat Disord; 2021 Aug; 89():17-21. PubMed ID: 34216936
[TBL] [Abstract][Full Text] [Related]
6. LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study.
Quadri M; Mandemakers W; Grochowska MM; Masius R; Geut H; Fabrizio E; Breedveld GJ; Kuipers D; Minneboo M; Vergouw LJM; Carreras Mascaro A; Yonova-Doing E; Simons E; Zhao T; Di Fonzo AB; Chang HC; Parchi P; Melis M; Correia Guedes L; Criscuolo C; Thomas A; Brouwer RWW; Heijsman D; Ingrassia AMT; Calandra Buonaura G; Rood JP; Capellari S; Rozemuller AJ; Sarchioto M; Fen Chien H; Vanacore N; Olgiati S; Wu-Chou YH; Yeh TH; Boon AJW; Hoogers SE; Ghazvini M; IJpma AS; van IJcken WFJ; Onofrj M; Barone P; Nicholl DJ; Puschmann A; De Mari M; Kievit AJ; Barbosa E; De Michele G; Majoor-Krakauer D; van Swieten JC; de Jong FJ; Ferreira JJ; Cossu G; Lu CS; Meco G; Cortelli P; van de Berg WDJ; Bonifati V;
Lancet Neurol; 2018 Jul; 17(7):597-608. PubMed ID: 29887161
[TBL] [Abstract][Full Text] [Related]
7. Mutation analysis of LRP10 in a large Chinese familial Parkinson disease cohort.
Li C; Chen Y; Ou R; Gu X; Wei Q; Cao B; Zhang L; Hou Y; Liu K; Chen X; Song W; Zhao B; Wu Y; Shang H
Neurobiol Aging; 2021 Mar; 99():99.e1-99.e6. PubMed ID: 32950273
[TBL] [Abstract][Full Text] [Related]
8. LRP10 Mutations May Correlate with Sporadic Parkinson's Disease in China.
Zhao Q; Ning P; Yang X; Shi C; Xu Y; Shen Q; Huang H; Xie D; Chen Y; Xu Y
Mol Neurobiol; 2021 Mar; 58(3):1212-1216. PubMed ID: 33118139
[TBL] [Abstract][Full Text] [Related]
9. Mutation analysis of LRP10 in Japanese patients with familial Parkinson's disease, progressive supranuclear palsy, and frontotemporal dementia.
Daida K; Nishioka K; Li Y; Yoshino H; Kikuchi A; Hasegawa T; Funayama M; Hattori N
Neurobiol Aging; 2019 Dec; 84():235.e11-235.e16. PubMed ID: 31582232
[TBL] [Abstract][Full Text] [Related]
10. Generation of an induced pluripotent stem cell (iPSC) line from a Parkinson's disease patient with a pathogenic LRP10/c.688C > T(p.Arg230Trp) mutation.
Wang Y; Wei C; Liu Y; Lu X; Wang W; Song N; Zhang W; Xu J; Zhang W; Han F
Stem Cell Res; 2024 Jun; 77():103359. PubMed ID: 38460235
[TBL] [Abstract][Full Text] [Related]
11. Analysis of p.Tyr307Asn variant in the LRP10 gene in Parkinson's disease in southern Spain.
Periñán MT; Macías-García D; Buiza-Rueda D; Guijarro-Albaladejo B; Jesús S; Adarmes-Gómez AD; Escuela R; Vigo-Ortega R; Gómez-Garre P; Mir P
Neurobiol Aging; 2020 Sep; 93():142.e1-142.e3. PubMed ID: 32409252
[TBL] [Abstract][Full Text] [Related]
12. Clinical and Pathological Phenotypes of LRP10 Variant Carriers with Dementia.
Vergouw LJM; Geut H; Breedveld G; Kuipers DJS; Quadri M; ; Rozemuller AJM; van Swieten JC; de Jong FJ; van de Berg WDJ; Bonifati V
J Alzheimers Dis; 2020; 76(3):1161-1170. PubMed ID: 32597809
[TBL] [Abstract][Full Text] [Related]
13. LRP10 variants in progressive supranuclear palsy.
Vergouw LJM; Melhem S; Donker Kaat L; Chiu WZ; Kuipers DJS; Breedveld G; Boon AJW; Wang LS; Naj AC; Mlynarksi E; Cantwell L; Quadri M; Ross OA; Dickson DW; Schellenberg GD; van Swieten JC; Bonifati V; de Jong FJ
Neurobiol Aging; 2020 Oct; 94():311.e5-311.e10. PubMed ID: 32527607
[TBL] [Abstract][Full Text] [Related]
14. Rare, pathogenic variants in LRP10 are associated with amyotrophic lateral sclerosis in patients from mainland China.
Ni J; Liu Z; Li W; Yuan Y; Huang L; Hu Y; Liu P; Hou X; Jiao B; Li J; Shen L; Jiang H; Tang B; Wang J
Neurobiol Aging; 2021 Jan; 97():145.e17-145.e22. PubMed ID: 32690342
[TBL] [Abstract][Full Text] [Related]
15. Analysis of the LRP10 gene in patients with Parkinson's disease and dementia with Lewy bodies from Southern Italy.
Gagliardi M; Procopio R; Nicoletti G; Morelli M; D'Amelio M; Quattrone A; Annesi G
Neurol Sci; 2021 Jan; 42(1):305-308. PubMed ID: 32995992
[TBL] [Abstract][Full Text] [Related]
16. Parkinson's disease-dementia in trans LRP10 and GBA variants: Response to deep brain stimulation.
Neri M; Braccia A; Panteghini C; Garavaglia B; Gualandi F; Cavallo MA; Scerrati A; Ferlini A; Sensi M
Parkinsonism Relat Disord; 2021 Nov; 92():72-75. PubMed ID: 34710740
[TBL] [Abstract][Full Text] [Related]
17. Genetic analysis of NUS1 in Chinese patients with Parkinson's disease.
Chen X; Xiao Y; Zhou M; Lin Y; Guo W; Huang S; Qiu J; Peng G; Mo M; Li Z; Zhu X; Xu P
Neurobiol Aging; 2020 Feb; 86():202.e5-202.e6. PubMed ID: 31582230
[TBL] [Abstract][Full Text] [Related]
18. Genetic analysis of the RAB39B gene in Chinese Han patients with Parkinson's disease.
Yuan L; Deng X; Song Z; Yang Z; Ni B; Chen Y; Deng H
Neurobiol Aging; 2015 Oct; 36(10):2907.e11-2. PubMed ID: 26163985
[TBL] [Abstract][Full Text] [Related]
19. TMEM230 mutation analysis in Parkinson's disease in a Chinese population.
Yan W; Tang B; Zhou X; Lei L; Li K; Sun Q; Xu Q; Yan X; Guo J; Liu Z
Neurobiol Aging; 2017 Jan; 49():219.e1-219.e3. PubMed ID: 27814995
[TBL] [Abstract][Full Text] [Related]
20. Analysis of EIF4G1 in ethnic Chinese.
Li K; Tang BS; Guo JF; Lou MX; Lv ZY; Liu ZH; Tian Y; Song CY; Xia K; Yan XX
BMC Neurol; 2013 Apr; 13():38. PubMed ID: 23617574
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
