793 related articles for article (PubMed ID: 23413260)
1. Glucocerebrosidase mutations influence the natural history of Parkinson's disease in a community-based incident cohort.
Winder-Rhodes SE; Evans JR; Ban M; Mason SL; Williams-Gray CH; Foltynie T; Duran R; Mencacci NE; Sawcer SJ; Barker RA
Brain; 2013 Feb; 136(Pt 2):392-9. PubMed ID: 23413260
[TBL] [Abstract][Full Text] [Related]
2. Glucocerebrosidase activity in Parkinson's disease with and without GBA mutations.
Alcalay RN; Levy OA; Waters CC; Fahn S; Ford B; Kuo SH; Mazzoni P; Pauciulo MW; Nichols WC; Gan-Or Z; Rouleau GA; Chung WK; Wolf P; Oliva P; Keutzer J; Marder K; Zhang X
Brain; 2015 Sep; 138(Pt 9):2648-58. PubMed ID: 26117366
[TBL] [Abstract][Full Text] [Related]
3. Features of
Malek N; Weil RS; Bresner C; Lawton MA; Grosset KA; Tan M; Bajaj N; Barker RA; Burn DJ; Foltynie T; Hardy J; Wood NW; Ben-Shlomo Y; Williams NW; Grosset DG; Morris HR;
J Neurol Neurosurg Psychiatry; 2018 Jul; 89(7):702-709. PubMed ID: 29378790
[TBL] [Abstract][Full Text] [Related]
4. β-Glucocerebrosidase gene mutations in two cohorts of Greek patients with sporadic Parkinson's disease.
Moraitou M; Hadjigeorgiou G; Monopolis I; Dardiotis E; Bozi M; Vassilatis D; Vilageliu L; Grinberg D; Xiromerisiou G; Stefanis L; Michelakakis H
Mol Genet Metab; 2011; 104(1-2):149-52. PubMed ID: 21745757
[TBL] [Abstract][Full Text] [Related]
5. Mutations in the glucocerebrosidase gene and Parkinson's disease in Ashkenazi Jews.
Aharon-Peretz J; Rosenbaum H; Gershoni-Baruch R
N Engl J Med; 2004 Nov; 351(19):1972-7. PubMed ID: 15525722
[TBL] [Abstract][Full Text] [Related]
6. Association of glucocerebrosidase polymorphisms and mutations with dementia in incident Parkinson's disease.
Lunde KA; Chung J; Dalen I; Pedersen KF; Linder J; Domellöf ME; Elgh E; Macleod AD; Tzoulis C; Larsen JP; Tysnes OB; Forsgren L; Counsell CE; Alves G; Maple-Grødem J
Alzheimers Dement; 2018 Oct; 14(10):1293-1301. PubMed ID: 29792872
[TBL] [Abstract][Full Text] [Related]
7. Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern Italy.
De Marco EV; Annesi G; Tarantino P; Rocca FE; Provenzano G; Civitelli D; Cirò Candiano IC; Annesi F; Carrideo S; Condino F; Nicoletti G; Messina D; Novellino F; Morelli M; Quattrone A
Mov Disord; 2008 Feb; 23(3):460-3. PubMed ID: 18074383
[TBL] [Abstract][Full Text] [Related]
8. Analysis of the glucocerebrosidase gene in Parkinson's disease.
Sato C; Morgan A; Lang AE; Salehi-Rad S; Kawarai T; Meng Y; Ray PN; Farrer LA; St George-Hyslop P; Rogaeva E
Mov Disord; 2005 Mar; 20(3):367-70. PubMed ID: 15517592
[TBL] [Abstract][Full Text] [Related]
9. Mutations in glucocerebrosidase are a major genetic risk factor for Parkinson's disease and increase susceptibility to dementia in a Flanders-Belgian cohort.
Crosiers D; Verstraeten A; Wauters E; Engelborghs S; Peeters K; Mattheijssens M; De Deyn PP; Theuns J; Van Broeckhoven C; Cras P
Neurosci Lett; 2016 Aug; 629():160-164. PubMed ID: 27397011
[TBL] [Abstract][Full Text] [Related]
10. GBA-associated Parkinson's disease: reduced survival and more rapid progression in a prospective longitudinal study.
Brockmann K; Srulijes K; Pflederer S; Hauser AK; Schulte C; Maetzler W; Gasser T; Berg D
Mov Disord; 2015 Mar; 30(3):407-11. PubMed ID: 25448271
[TBL] [Abstract][Full Text] [Related]
11. Association between Parkinson's disease and glucocerebrosidase mutations in Brazil.
Spitz M; Rozenberg R; Pereira Lda V; Reis Barbosa E
Parkinsonism Relat Disord; 2008; 14(1):58-62. PubMed ID: 17703984
[TBL] [Abstract][Full Text] [Related]
12. Parkinson's disease in patients and obligate carriers of Gaucher disease.
Becker JG; Pastores GM; Di Rocco A; Ferraris M; Graber JJ; Sathe S
Parkinsonism Relat Disord; 2013 Jan; 19(1):129-31. PubMed ID: 22940477
[TBL] [Abstract][Full Text] [Related]
13. Mutations in the glucocerebrosidase gene and Parkinson disease: phenotype-genotype correlation.
Aharon-Peretz J; Badarny S; Rosenbaum H; Gershoni-Baruch R
Neurology; 2005 Nov; 65(9):1460-1. PubMed ID: 16148263
[TBL] [Abstract][Full Text] [Related]
14. Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease.
Clark LN; Ross BM; Wang Y; Mejia-Santana H; Harris J; Louis ED; Cote LJ; Andrews H; Fahn S; Waters C; Ford B; Frucht S; Ottman R; Marder K
Neurology; 2007 Sep; 69(12):1270-7. PubMed ID: 17875915
[TBL] [Abstract][Full Text] [Related]
15. Cognitive impairment in carriers of glucocerebrosidase gene mutation in Parkinson disease patients.
Malec-Litwinowicz M; Rudzińska M; Szubiga M; Michalski M; Tomaszewski T; Szczudlik A
Neurol Neurochir Pol; 2014; 48(4):258-61. PubMed ID: 25168325
[TBL] [Abstract][Full Text] [Related]
16. Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease.
Neumann J; Bras J; Deas E; O'Sullivan SS; Parkkinen L; Lachmann RH; Li A; Holton J; Guerreiro R; Paudel R; Segarane B; Singleton A; Lees A; Hardy J; Houlden H; Revesz T; Wood NW
Brain; 2009 Jul; 132(Pt 7):1783-94. PubMed ID: 19286695
[TBL] [Abstract][Full Text] [Related]
17. White matter abnormalities in Parkinson's disease patients with glucocerebrosidase gene mutations.
Agosta F; Kostic VS; Davidovic K; Kresojević N; Sarro L; Svetel M; Stanković I; Comi G; Klein C; Filippi M
Mov Disord; 2013 Jun; 28(6):772-8. PubMed ID: 23418083
[TBL] [Abstract][Full Text] [Related]
18. Advances in GBA-associated Parkinson's disease--Pathology, presentation and therapies.
Barkhuizen M; Anderson DG; Grobler AF
Neurochem Int; 2016 Feb; 93():6-25. PubMed ID: 26743617
[TBL] [Abstract][Full Text] [Related]
19. Mutations in the glucocerebrosidase gene are common in patients with Parkinson's disease from Eastern Canada.
Han F; Grimes DA; Li F; Wang T; Yu Z; Song N; Wu S; Racacho L; Bulman DE
Int J Neurosci; 2016; 126(5):415-21. PubMed ID: 26000814
[TBL] [Abstract][Full Text] [Related]
20. GBA Variants Influence Motor and Non-Motor Features of Parkinson's Disease.
Jesús S; Huertas I; Bernal-Bernal I; Bonilla-Toribio M; Cáceres-Redondo MT; Vargas-González L; Gómez-Llamas M; Carrillo F; Calderón E; Carballo M; Gómez-Garre P; Mir P
PLoS One; 2016; 11(12):e0167749. PubMed ID: 28030538
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
