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13,552 results
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Gambling and Parkinson disease.
Lu C, Bharmal A, Suchowersky O. Lu C, et al. Arch Neurol. 2006 Feb;63(2):298. doi: 10.1001/archneur.63.2.298-a. Arch Neurol. 2006. PMID: 16476827 No abstract available.
Mitochondrial DNA variants as genetic risk factors for Parkinson disease.
Liou CW, Chuang JH, Chen JB, Tiao MM, Wang PW, Huang ST, Huang TL, Lee WC, Weng SW, Huang PH, Chen SD, Chen RS, Lu CS, Lin TK. Liou CW, et al. Among authors: lu cs. Eur J Neurol. 2016 Aug;23(8):1289-300. doi: 10.1111/ene.13020. Epub 2016 May 10. Eur J Neurol. 2016. PMID: 27160373
Environmental risk factors of young onset Parkinson's disease: a case-control study.
Tsai CH, Lo SK, See LC, Chen HZ, Chen RS, Weng YH, Chang FC, Lu CS. Tsai CH, et al. Among authors: lu cs. Clin Neurol Neurosurg. 2002 Sep;104(4):328-33. doi: 10.1016/s0303-8467(02)00027-6. Clin Neurol Neurosurg. 2002. PMID: 12140099
PARK6-linked autosomal recessive early-onset parkinsonism in Asian populations.
Hatano Y, Sato K, Elibol B, Yoshino H, Yamamura Y, Bonifati V, Shinotoh H, Asahina M, Kobayashi S, Ng AR, Rosales RL, Hassin-Baer S, Shinar Y, Lu CS, Chang HC, Wu-Chou YH, AtaƧ FB, Kobayashi T, Toda T, Mizuno Y, Hattori N. Hatano Y, et al. Among authors: lu cs. Neurology. 2004 Oct 26;63(8):1482-5. doi: 10.1212/01.wnl.0000142258.29304.fe. Neurology. 2004. PMID: 15505170
Analysis of the UCHL1 genetic variant in Parkinson's disease among Chinese.
Tan EK, Lu CS, Peng R, Teo YY, Wu-Chou YH, Chen RS, Weng YH, Chen CM, Fung HC, Tan LC, Zhang ZJ, An XK, Lee-Chen GJ, Lee MC, Fook-Chong S, Burgunder JM, Wu RM, Wu YR. Tan EK, et al. Among authors: lu cs. Neurobiol Aging. 2010 Dec;31(12):2194-6. doi: 10.1016/j.neurobiolaging.2008.11.008. Epub 2009 Mar 28. Neurobiol Aging. 2010. PMID: 19329225
The LRRK2 Gly2385Arg variant is associated with Parkinson's disease: genetic and functional evidence.
Tan EK, Zhao Y, Skipper L, Tan MG, Di Fonzo A, Sun L, Fook-Chong S, Tang S, Chua E, Yuen Y, Tan L, Pavanni R, Wong MC, Kolatkar P, Lu CS, Bonifati V, Liu JJ. Tan EK, et al. Among authors: lu cs. Hum Genet. 2007 Feb;120(6):857-63. doi: 10.1007/s00439-006-0268-0. Epub 2006 Sep 30. Hum Genet. 2007. PMID: 17019612
LRRK2 G2385R modulates age at onset in Parkinson's disease: A multi-center pooled analysis.
Tan EK, Peng R, Wu YR, Wu RM, Wu-Chou YH, Tan LC, An XK, Chen CM, Fook-Chong S, Lu CS. Tan EK, et al. Among authors: lu cs. Am J Med Genet B Neuropsychiatr Genet. 2009 Oct 5;150B(7):1022-3. doi: 10.1002/ajmg.b.30923. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 19152345 No abstract available.
Long-term outcomes of arrhythmia and distinct electrophysiological features in congenitally corrected transposition of the great arteries in an Asian cohort.
Tseng WC, Huang CN, Chiu SN, Lu CW, Wang JK, Lin MT, Chen CA, Wu MH. Tseng WC, et al. Among authors: lu cw. Am Heart J. 2020 Oct 21:S0002-8703(20)30343-4. doi: 10.1016/j.ahj.2020.10.057. Online ahead of print. Am Heart J. 2020. PMID: 33098810
Expert consensus on optimal acquisition and development of the International Bowel Ultrasound Segmental Activity Score (IBUS-SAS): a reliability and inter-rater variability study on intestinal ultrasonography in Crohn's Disease.
Novak KL, Nylund K, Maaser C, Petersen F, Kucharzik T, Lu C, Allocca M, Maconi G, de Voogd F, Christensen B, Vaughan R, Palmela C, Carter D, Wilkens R. Novak KL, et al. Among authors: lu c. J Crohns Colitis. 2020 Oct 24:jjaa216. doi: 10.1093/ecco-jcc/jjaa216. Online ahead of print. J Crohns Colitis. 2020. PMID: 33098642
Author Correction: Combined Tissue-Fluid Proteomics to Unravel Phenotypic Variability in Amyotrophic Lateral Sclerosis.
Leoni E, Bremang M, Mitra V, Zubiri I, Jung S, Lu CH, Adiutori R, Lombardi V, Russell C, Koncarevic S, Ward M, Pike I, Malaspina A. Leoni E, et al. Among authors: lu ch. Sci Rep. 2020 Oct 23;10(1):18603. doi: 10.1038/s41598-020-74974-1. Sci Rep. 2020. PMID: 33097756
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