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.
58 related articles for article (PubMed ID: 19879328)
1. Genetic analysis of the NEUROG2 gene in patients with Parkinson's disease. Deng S; Deng H; Le W; Xu H; Yang H; Deng X; Lv H; Xie W; Zhu S; Jankovic J Neurosci Lett; 2010 Jan; 468(3):195-7. PubMed ID: 19879328 [TBL] [Abstract][Full Text] [Related]
2. Examination of the MASH1 gene in patients with Parkinson's disease. Deng H; Yang H; Le W; Deng X; Xu H; Xiong W; Zhu S; Xie W; Song Z; Jankovic J Biochem Biophys Res Commun; 2010 Feb; 392(4):548-50. PubMed ID: 20097173 [TBL] [Abstract][Full Text] [Related]
3. Examination of the MSX1 gene in patients with Parkinson's disease. Deng H; Zhu SH; Le WD; Yang HR; Lv HW; Xu HB; Xie WJ; Jankovic J Acta Neurol Scand; 2009 Dec; 120(6):442-4. PubMed ID: 19922584 [TBL] [Abstract][Full Text] [Related]
4. Systematic genetic analysis of the PITX3 gene in patients with Parkinson disease. Guo Y; Le WD; Jankovic J; Yang HR; Xu HB; Xie WJ; Song Z; Deng H Mov Disord; 2011 Aug; 26(9):1729-32. PubMed ID: 21469209 [TBL] [Abstract][Full Text] [Related]
5. Translated mutation in the Nurr1 gene as a cause for Parkinson's disease. Grimes DA; Han F; Panisset M; Racacho L; Xiao F; Zou R; Westaff K; Bulman DE Mov Disord; 2006 Jul; 21(7):906-9. PubMed ID: 16532445 [TBL] [Abstract][Full Text] [Related]
6. Association of a variation in the promoter region of the brain-derived neurotrophic factor gene with familial Parkinson's disease. Parsian A; Sinha R; Racette B; Zhao JH; Perlmutter JS Parkinsonism Relat Disord; 2004 Jun; 10(4):213-9. PubMed ID: 15120095 [TBL] [Abstract][Full Text] [Related]
7. Mutation analysis of the glial cell line-derived neurotrophic factor gene in Parkinson's disease. Wartiovaara K; Hytönen M; Vuori M; Paulin L; Rinne J; Sariola H Exp Neurol; 1998 Aug; 152(2):307-9. PubMed ID: 9710530 [TBL] [Abstract][Full Text] [Related]
8. The transcription factor PITX3 is associated with sporadic Parkinson's disease. Fuchs J; Mueller JC; Lichtner P; Schulte C; Munz M; Berg D; Wüllner U; Illig T; Sharma M; Gasser T Neurobiol Aging; 2009 May; 30(5):731-8. PubMed ID: 17905480 [TBL] [Abstract][Full Text] [Related]
9. Heredity in Parkinson's disease: new findings. Lev N; Melamed E Isr Med Assoc J; 2001 Jun; 3(6):435-8. PubMed ID: 11433638 [TBL] [Abstract][Full Text] [Related]
10. Low frequency of alpha-synuclein mutations in familial Parkinson's disease. Farrer M; Wavrant-De Vrieze F; Crook R; Boles L; Perez-Tur J; Hardy J; Johnson WG; Steele J; Maraganore D; Gwinn K; Lynch T Ann Neurol; 1998 Mar; 43(3):394-7. PubMed ID: 9506559 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. CARD15 variants in patients with sporadic Parkinson's disease. Bialecka M; Kurzawski M; Klodowska-Duda G; Opala G; Juzwiak S; Kurzawski G; Tan EK; Drozdzik M Neurosci Res; 2007 Mar; 57(3):473-6. PubMed ID: 17174426 [TBL] [Abstract][Full Text] [Related]
13. Mutational screening of the mitochondrial transcription factors B1 and B2 (TFB1M and TFB2M) in Parkinson's disease. Sánchez-Ferrero E; Coto E; Blázquez M; Ribacoba R; Guisasola LM; Salvador C; Alvarez V Parkinsonism Relat Disord; 2009 Jul; 15(6):468-70. PubMed ID: 18980857 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Mitochondrial transcription factor A (TFAM) gene variation in Parkinson's disease. Alvarez V; Corao AI; Sánchez-Ferrero E; De Mena L; Alonso-Montes C; Huerta C; Blázquez M; Ribacoba R; Guisasola LM; Salvador C; García-Castro M; Coto E Neurosci Lett; 2008 Feb; 432(1):79-82. PubMed ID: 18248889 [TBL] [Abstract][Full Text] [Related]
16. DNA sequence analysis of monoamine oxidase B gene coding and promoter regions in Parkinson's disease cases and unrelated controls. Costa-Mallen P; Afsharinejad Z; Kelada SN; Costa LG; Franklin GM; Swanson PD; Longstreth WT; Viernes HM; Farin FM; Smith-Weller T; Checkoway H Mov Disord; 2004 Jan; 19(1):76-83. PubMed ID: 14743364 [TBL] [Abstract][Full Text] [Related]
17. Evaluation of the role of Nurr1 in a large sample of familial Parkinson's disease. Nichols WC; Uniacke SK; Pankratz N; Reed T; Simon DK; Halter C; Rudolph A; Shults CW; Conneally PM; Foroud T; Mov Disord; 2004 Jun; 19(6):649-55. PubMed ID: 15197702 [TBL] [Abstract][Full Text] [Related]
19. [Association between dopamine transporter gene polymorphism and Parkinson's disease]. Zhang L; Shao M; Xu Q; Dong X; Yang J; Li Y; Chen B Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Dec; 18(6):431-4. PubMed ID: 11774209 [TBL] [Abstract][Full Text] [Related]
20. [Progress in the basic and clinical aspects of Parkinson's disease]. Mizuno Y Rinsho Shinkeigaku; 2004 Nov; 44(11):741-50. PubMed ID: 15651281 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]