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Page 1
Progressive Supranuclear Palsy in India: Past, Present, and Future.
Raju S, Shetty K, Sahoo L, Paramanandam V, Iyer JM, Bowmick S, Desai S, Joshi D, Kumar N, Mehta S, Kandadai RM, Wadia P, Biswas A, Garg D, Agarwal P, Krishnan S, Ganguly J, Shah H, Chandarana M, Kumar H, Borgohain R, Ramprasad VL, Kukkle PL; PRAI Consortium. Raju S, et al. Among authors: kukkle pl. Ann Indian Acad Neurol. 2024 Dec 2. doi: 10.4103/aian.aian_515_24. Online ahead of print. Ann Indian Acad Neurol. 2024. PMID: 39620998 Free article.
Exercise Habits in People with Parkinson's: A Multinational Survey.
Jagota P, Phutrakool P, Kamble N, Dang THT, Aldaajani Z, Hatano T, Hoskere Sreenivasa DK, Tripura T, Kukkle PL, Jeon B, Nishikawa N, Oji Y, Tran TN, Susatia F, Fabbri M, Leung C, Alonso Canovas A, Kamel WA, Pal PK, Rakesh K, Abu Snineh M, Chairangsaris P, Lolekha P, Jamora RDG, Mohamed Ibrahim N, Desa SHM, Tan AH, Toh TS, Obaid M, Fung VSC, Lang A, Lin CH, Regragui W, Bouslam N, Bhidayasiri R. Jagota P, et al. Among authors: kukkle pl. Mov Disord Clin Pract. 2024 Nov;11(11):1396-1409. doi: 10.1002/mdc3.14197. Epub 2024 Aug 29. Mov Disord Clin Pract. 2024. PMID: 39206964
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
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.
The Genetic Drivers of Juvenile, Young, and Early-Onset Parkinson's Disease in India.
Andrews SV, Kukkle PL, Menon R, Geetha TS, Goyal V, Kandadai RM, Kumar H, Borgohain R, Mukherjee A, Wadia PM, Yadav R, Desai S, Kumar N, Joshi D, Murugan S, Biswas A, Pal PK, Oliver M, Nair S, Kayalvizhi A, Samson PL, Deshmukh M, Bassi A, Sandeep C, Mandloi N, Davis OB, Roberts MA, Leto DE, Henry AG, Di Paolo G, Muthane U, Das SK, Peterson AS, Sandmann T, Gupta R, Ramprasad VL; Parkinson Research Alliance of India (PRAI). Andrews SV, et al. Among authors: kukkle pl. Mov Disord. 2024 Feb;39(2):339-349. doi: 10.1002/mds.29676. Epub 2023 Nov 28. Mov Disord. 2024. PMID: 38014556
Author Correction: Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2).
Lange LM, Avenali M, Ellis M, Illarionova A, Keller Sarmiento IJ, Tan AH, Madoev H, Galandra C, Junker J, Roopnarain K, Solle J, Wegel C, Fang ZH, Heutink P, Kumar KR, Lim SY, Valente EM, Nalls M, Blauwendraat C, Singleton A, Mencacci N, Lohmann K, Klein C; Global Parkinson’s Genetic Program (GP2). Lange LM, et al. NPJ Parkinsons Dis. 2023 Sep 13;9(1):133. doi: 10.1038/s41531-023-00560-7. NPJ Parkinsons Dis. 2023. PMID: 37704671 Free PMC article. No abstract available.
Defining the causes of sporadic Parkinson's disease in the global Parkinson's genetics program (GP2).
Towns C, Richer M, Jasaityte S, Stafford EJ, Joubert J, Antar T, Martinez-Carrasco A, Makarious MB, Casey B, Vitale D, Levine K, Leonard H, Pantazis CB, Screven LA, Hernandez DG, Wegel CE, Solle J, Nalls MA, Blauwendraat C, Singleton AB, Tan MMX, Iwaki H, Morris HR; Global Parkinson’s Genetics Program (GP2). Towns C, et al. NPJ Parkinsons Dis. 2023 Sep 12;9(1):131. doi: 10.1038/s41531-023-00533-w. NPJ Parkinsons Dis. 2023. PMID: 37699923 Free PMC article.
30 results