399 related articles for article (PubMed ID: 33579389)
1. Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson's disease.
Smolders S; Philtjens S; Crosiers D; Sieben A; Hens E; Heeman B; Van Mossevelde S; Pals P; Asselbergh B; Dos Santos Dias R; Vermeiren Y; Vandenberghe R; Engelborghs S; De Deyn PP; Martin JJ; Cras P; Annaert W; Van Broeckhoven C;
Acta Neuropathol Commun; 2021 Feb; 9(1):25. PubMed ID: 33579389
[TBL] [Abstract][Full Text] [Related]
2. VPS13C-associated Parkinson's disease: Two novel cases and review of the literature.
Monfrini E; Spagnolo F; Canesi M; Seresini A; Rini A; Passarella B; Percetti M; Seia M; Goldwurm S; Cereda V; Comi GP; Pezzoli G; Di Fonzo A
Parkinsonism Relat Disord; 2022 Jan; 94():37-39. PubMed ID: 34875562
[TBL] [Abstract][Full Text] [Related]
3. Mutation screening and burden analysis of VPS13C in Chinese patients with early-onset Parkinson's disease.
Gu X; Li C; Chen Y; Ou R; Cao B; Wei Q; Hou Y; Zhang L; Song W; Zhao B; Wu Y; Shang H
Neurobiol Aging; 2020 Oct; 94():311.e1-311.e4. PubMed ID: 32507414
[TBL] [Abstract][Full Text] [Related]
4. ADNC-RS, a clinical-genetic risk score, predicts Alzheimer's pathology in autopsy-confirmed Parkinson's disease and Dementia with Lewy bodies.
Dai DL; Tropea TF; Robinson JL; Suh E; Hurtig H; Weintraub D; Van Deerlin V; Lee EB; Trojanowski JQ; Chen-Plotkin AS
Acta Neuropathol; 2020 Oct; 140(4):449-461. PubMed ID: 32749525
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Association between CSF alpha-synuclein seeding activity and genetic status in Parkinson's disease and dementia with Lewy bodies.
Brockmann K; Quadalti C; Lerche S; Rossi M; Wurster I; Baiardi S; Roeben B; Mammana A; Zimmermann M; Hauser AK; Deuschle C; Schulte C; Waniek K; Lachmann I; Sjödin S; Brinkmalm A; Blennow K; Zetterberg H; Gasser T; Parchi P
Acta Neuropathol Commun; 2021 Oct; 9(1):175. PubMed ID: 34717775
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy.
Lesage S; Drouet V; Majounie E; Deramecourt V; Jacoupy M; Nicolas A; Cormier-Dequaire F; Hassoun SM; Pujol C; Ciura S; Erpapazoglou Z; Usenko T; Maurage CA; Sahbatou M; Liebau S; Ding J; Bilgic B; Emre M; Erginel-Unaltuna N; Guven G; Tison F; Tranchant C; Vidailhet M; Corvol JC; Krack P; Leutenegger AL; Nalls MA; Hernandez DG; Heutink P; Gibbs JR; Hardy J; Wood NW; Gasser T; Durr A; Deleuze JF; Tazir M; Destée A; Lohmann E; Kabashi E; Singleton A; Corti O; Brice A; ;
Am J Hum Genet; 2016 Mar; 98(3):500-513. PubMed ID: 26942284
[TBL] [Abstract][Full Text] [Related]
9. Clinicopathologic and genetic features of multiple system atrophy with Lewy body disease.
Koga S; Li F; Zhao N; Roemer SF; Ferman TJ; Wernick AI; Walton RL; Faroqi AH; Graff-Radford NR; Cheshire WP; Ross OA; Dickson DW
Brain Pathol; 2020 Jul; 30(4):766-778. PubMed ID: 32232888
[TBL] [Abstract][Full Text] [Related]
10. Contribution of homozygous and compound heterozygous missense mutations in VWA2 to Alzheimer's disease.
Hoogmartens J; Hens E; Engelborghs S; Vandenberghe R; De Deyn PP; Cacace R; Van Broeckhoven C;
Neurobiol Aging; 2021 Mar; 99():100.e17-100.e23. PubMed ID: 33023779
[TBL] [Abstract][Full Text] [Related]
11. The alpha-synucleinopathies: Parkinson's disease, dementia with Lewy bodies, and multiple system atrophy.
Spillantini MG; Goedert M
Ann N Y Acad Sci; 2000; 920():16-27. PubMed ID: 11193145
[TBL] [Abstract][Full Text] [Related]
12. Genetic association study of synphilin-1 in idiopathic Parkinson's disease.
Myhre R; Klungland H; Farrer MJ; Aasly JO
BMC Med Genet; 2008 Mar; 9():19. PubMed ID: 18366718
[TBL] [Abstract][Full Text] [Related]
13. Association of ABI3 and PLCG2 missense variants with disease risk and neuropathology in Lewy body disease and progressive supranuclear palsy.
Strickland SL; Morel H; Prusinski C; Allen M; Patel TA; Carrasquillo MM; Conway OJ; Lincoln SJ; Reddy JS; Nguyen T; Malphrus KG; Soto AI; Walton RL; Crook JE; Murray ME; Boeve BF; Petersen RC; Lucas JA; Ferman TJ; Uitti RJ; Wszolek ZK; Ross OA; Graff-Radford NR; Dickson DW; Ertekin-Taner N
Acta Neuropathol Commun; 2020 Oct; 8(1):172. PubMed ID: 33092647
[TBL] [Abstract][Full Text] [Related]
14. Lewy- and Alzheimer-type pathologies in midbrain and cerebellum across the Lewy body disorders spectrum.
Sierra M; Gelpi E; Martí MJ; Compta Y
Neuropathol Appl Neurobiol; 2016 Aug; 42(5):451-62. PubMed ID: 26810462
[TBL] [Abstract][Full Text] [Related]
15. Beta-synuclein gene alterations in dementia with Lewy bodies.
Ohtake H; Limprasert P; Fan Y; Onodera O; Kakita A; Takahashi H; Bonner LT; Tsuang DW; Murray IV; Lee VM; Trojanowski JQ; Ishikawa A; Idezuka J; Murata M; Toda T; Bird TD; Leverenz JB; Tsuji S; La Spada AR
Neurology; 2004 Sep; 63(5):805-11. PubMed ID: 15365127
[TBL] [Abstract][Full Text] [Related]
16. Neuropathological and genetic characteristics of a post-mortem series of cases with dementia with Lewy bodies clinically suspected of Creutzfeldt-Jakob's disease.
Geut H; Vergouw LJM; Galis Y; Ingrassia A; de Jong FJ; Quadri M; Bonifati V; Lemstra AW; Rozemuller AJM; van de Berg WDJ
Parkinsonism Relat Disord; 2019 Jun; 63():162-168. PubMed ID: 30777654
[TBL] [Abstract][Full Text] [Related]
17. A soluble tau fragment generated by caspase-2 is associated with dementia in Lewy body disease.
Smith BR; Nelson KM; Kemper LJ; Leinonen-Wright K; Petersen A; Keene CD; Ashe KH
Acta Neuropathol Commun; 2019 Jul; 7(1):124. PubMed ID: 31362787
[TBL] [Abstract][Full Text] [Related]
18. GRN Mutations Are Associated with Lewy Body Dementia.
Reho P; Koga S; Shah Z; Chia R; ; ; Rademakers R; Dalgard CL; Boeve BF; Beach TG; Dickson DW; Ross OA; Scholz SW
Mov Disord; 2022 Sep; 37(9):1943-1948. PubMed ID: 35810449
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]
