These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
299 related articles for article (PubMed ID: 17703984)
21. Glucocerebrosidase gene L444P mutation is a risk factor for Parkinson's disease in Chinese population. Sun QY; Guo JF; Wang L; Yu RH; Zuo X; Yao LY; Pan Q; Xia K; Tang BS Mov Disord; 2010 Jun; 25(8):1005-11. PubMed ID: 20131388 [TBL] [Abstract][Full Text] [Related]
23. Mutations of glucocerebrosidase gene and susceptibility to Parkinson's disease: An updated meta-analysis in a European population. Zhao F; Bi L; Wang W; Wu X; Li Y; Gong F; Lu S; Feng F; Qian Z; Hu C; Wu Y; Sun Y Neuroscience; 2016 Apr; 320():239-46. PubMed ID: 26868973 [TBL] [Abstract][Full Text] [Related]
24. Parkinson's disease and the heterozygous state for glucocerebrosidase mutations among Brazilians. Socal MP; Bock H; Michelin-Tirelli K; Hilbig A; Saraiva-Pereira ML; Rieder CR; Jardim LB Parkinsonism Relat Disord; 2009 Jan; 15(1):76-8. PubMed ID: 18358758 [No Abstract] [Full Text] [Related]
25. Gaucher disease: complexity in a "simple" disorder. Sidransky E Mol Genet Metab; 2004; 83(1-2):6-15. PubMed ID: 15464415 [TBL] [Abstract][Full Text] [Related]
26. Mutational analysis of GIGYF2, ATP13A2 and GBA genes in Brazilian patients with early-onset Parkinson's disease. Dos Santos AV; Pestana CP; Diniz KR; Campos M; Abdalla-Carvalho CB; de Rosso AL; Pereira JS; Nicaretta DH; de Carvalho WL; Dos Santos JM; Santos-Rebouças CB; Pimentel MM Neurosci Lett; 2010 Nov; 485(2):121-4. PubMed ID: 20816920 [TBL] [Abstract][Full Text] [Related]
28. Mutations in GBA and risk of Parkinson's disease: a meta-analysis based on 25 case-control studies. Mao X; Wang T; Peng R; Chang X; Li N; Gu Y; Zhao D; Liao Q; Liu M Neurol Res; 2013 Oct; 35(8):873-8. PubMed ID: 23676350 [TBL] [Abstract][Full Text] [Related]
29. Osteopontin polymorphic susceptibility factor for Parkinson's disease among patients with Gaucher disease. Ribner A; Altarescu G; Zimran A; Elstein D Mov Disord; 2011 Jun; 26(7):1341-3. PubMed ID: 21469198 [TBL] [Abstract][Full Text] [Related]
30. Glucocerebrosidase L444P mutation confers genetic risk for Parkinson's disease in central China. Wang Y; Liu L; Xiong J; Zhang X; Chen Z; Yu L; Chen C; Huang J; Zhang Z; Mohmed AA; Lin Z; Xiong N; Wang T Behav Brain Funct; 2012 Dec; 8():57. PubMed ID: 23227814 [TBL] [Abstract][Full Text] [Related]
31. 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]
34. Association of mutations in the glucocerebrosidase gene with Parkinson disease in a Korean population. Choi JM; Kim WC; Lyoo CH; Kang SY; Lee PH; Baik JS; Koh SB; Ma HI; Sohn YH; Lee MS; Kim YJ Neurosci Lett; 2012 Apr; 514(1):12-5. PubMed ID: 22387070 [TBL] [Abstract][Full Text] [Related]
35. Complete screening for glucocerebrosidase mutations in Parkinson disease patients from Greece. Kalinderi K; Bostantjopoulou S; Paisan-Ruiz C; Katsarou Z; Hardy J; Fidani L Neurosci Lett; 2009 Mar; 452(2):87-9. PubMed ID: 19383421 [TBL] [Abstract][Full Text] [Related]
36. Strong association between glucocerebrosidase mutations and Parkinson's disease in Sweden. Ran C; Brodin L; Forsgren L; Westerlund M; Ramezani M; Gellhaar S; Xiang F; Fardell C; Nissbrandt H; Söderkvist P; Puschmann A; Ygland E; Olson L; Willows T; Johansson A; Sydow O; Wirdefeldt K; Galter D; Svenningsson P; Belin AC Neurobiol Aging; 2016 Sep; 45():212.e5-212.e11. PubMed ID: 27255555 [TBL] [Abstract][Full Text] [Related]
37. [Association between the debrisoquine hydroxylase gene polymorphism and the genetic susceptibility of Parkinson's disease]. Tao E; Liu Z; Chen B; Pan X; Shao M Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1998 Oct; 15(5):281-3. PubMed ID: 9758873 [TBL] [Abstract][Full Text] [Related]
38. 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]
40. [Detection of the frequencies of GBA gene major mutations in patients with Gaucher disease in Ukraine]. Horovenko NH; Ol'khovych NV; Nedoboĭ AM; Pichkur NO Tsitol Genet; 2007; 41(4):41-7. PubMed ID: 18030725 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]