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34 results

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Page 1
Multi-ancestry genome-wide association meta-analysis of Parkinson's disease.
Kim JJ, Vitale D, Otani DV, Lian MM, Heilbron K; 23andMe Research Team; Iwaki H, Lake J, Solsberg CW, Leonard H, Makarious MB, Tan EK, Singleton AB, Bandres-Ciga S, Noyce AJ; Global Parkinson’s Genetics Program (GP2); Blauwendraat C, Nalls MA, Foo JN, Mata I. Kim JJ, et al. Nat Genet. 2024 Jan;56(1):27-36. doi: 10.1038/s41588-023-01584-8. Epub 2023 Dec 28. Nat Genet. 2024. PMID: 38155330 Free PMC article.
Post-dengue parkinsonism.
Azmin S, Sahathevan R, Suehazlyn Z, Law ZK, Rabani R, Nafisah WY, Tan HJ, Norlinah MI. Azmin S, et al. Among authors: norlinah mi. BMC Infect Dis. 2013 Apr 18;13:179. doi: 10.1186/1471-2334-13-179. BMC Infect Dis. 2013. PMID: 23594500 Free PMC article.
Tuberculous meningitis mimicking Creutzfeldt-Jakob disease.
Khoo CS, Krishnan L, Ng CF, Teh PC, Norlinah MI, Tan HJ. Khoo CS, et al. Among authors: norlinah mi. Rev Neurol (Paris). 2021 Mar;177(3):319-321. doi: 10.1016/j.neurol.2020.05.013. Epub 2020 Jul 31. Rev Neurol (Paris). 2021. PMID: 32747046 No abstract available.
The LRRK2 p.L1795F variant causes Parkinson's disease in the European population.
Lange LM, Levine K, Fox SH, Marras C, Ahmed N, Kuznetsov N, Vitale D, Iwaki H, Lohmann K, Marsili L, Espay AJ, Bauer P, Beetz C, Martin J, Factor SA, Higginbotham LA, Chen H, Leonard H, Nalls MA, Mencacci NE, Morris HR, Singleton AB, Klein C, Blauwendraat C, Fang ZH; Global Parkinson’s Genetics Program (GP2). Lange LM, et al. NPJ Parkinsons Dis. 2025 Mar 25;11(1):58. doi: 10.1038/s41531-025-00896-2. NPJ Parkinsons Dis. 2025. PMID: 40133296 Free PMC article.
Insights into ancestral diversity in Parkinson's disease risk: a comparative assessment of polygenic risk scores.
Saffie-Awad P, Grant SM, Makarious MB, Elsayed I, Sanyaolu AO, Crea PW, Schumacher Schuh AF, Levine KS, Vitale D, Koretsky MJ, Kim J, Peixoto Leal T, Periñán MT, Dey S, Noyce AJ, Reyes-Palomares A, Rodriguez-Losada N, Foo JN, Mohamed W, Heilbron K, Norcliffe-Kaufmann L; 23andMe Research Team; Rizig M, Okubadejo N, Nalls MA, Blauwendraat C, Singleton A, Leonard H; Global Parkinson’s Genetics Program (GP2); Mata IF, Bandres-Ciga S. Saffie-Awad P, et al. NPJ Parkinsons Dis. 2025 Jul 3;11(1):201. doi: 10.1038/s41531-025-00967-4. NPJ Parkinsons Dis. 2025. PMID: 40610451 Free PMC article.
Review of emotion recognition in stroke patients.
Yuvaraj R, Murugappan M, Norlinah MI, Sundaraj K, Khairiyah M. Yuvaraj R, et al. Among authors: norlinah mi. Dement Geriatr Cogn Disord. 2013;36(3-4):179-96. doi: 10.1159/000353440. Epub 2013 Jul 26. Dement Geriatr Cogn Disord. 2013. PMID: 23899462 Review.
PARK16 is associated with PD in the Malaysian population.
Gopalai AA, Ahmad-Annuar A, Li HH, Zhao Y, Lim SY, Tan AH, Lim TT, Eow GB, Santhi P, Shanthi V, Norlinah MI, Aziz ZA, Lim SK, Tan CT, Tan EK. Gopalai AA, et al. Among authors: norlinah mi. Am J Med Genet B Neuropsychiatr Genet. 2016 Sep;171(6):839-47. doi: 10.1002/ajmg.b.32454. Epub 2016 May 13. Am J Med Genet B Neuropsychiatr Genet. 2016. PMID: 27174169
GBA1 rs3115534 Is Associated with REM Sleep Behavior Disorder in Parkinson's Disease in Nigerians.
Ojo OO, Bandres-Ciga S, Makarious MB, Crea PW, Hernandez DG, Houlden H, Rizig M, Singleton AB, Noyce AJ, Nalls MA, Blauwendraat C, Okubadejo NU; Nigeria Parkinson's Disease Research Network and the Global Parkinson's Genetics Program (GP2). Ojo OO, et al. Mov Disord. 2024 Apr;39(4):728-733. doi: 10.1002/mds.29753. Epub 2024 Feb 23. Mov Disord. 2024. PMID: 38390630 Free PMC article.
Role of high resolution ultrasound in ulnar nerve neuropathy.
Radhika S, Lee YL, Low SF, Fazalina MF, Sharifah Majedah IA, Suraya A, Rajesh S, Jamari S, Tan HJ, Norlinah MI. Radhika S, et al. Among authors: norlinah mi. Med J Malaysia. 2015 Jun;70(3):158-61. Med J Malaysia. 2015. PMID: 26248778 Free article.
34 results