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Biomed Research International|September 23, 2014
LRRK2 G2385R and R1628P mutations are associated with an increased risk of Parkinson's disease in the Malaysian populationAroma Agape Gopalai, Shen-Yang Lim, Jing Yi Chua, et al.
Neurobiology of Aging|March 31, 2009
Analysis of the UCHL1 genetic variant in Parkinson's disease among ChineseE K Tan, C S Lu, R Peng, et al.
Nature Genetics|November 15, 2011
Genome-wide association study identifies FCGR2A as a susceptibility locus for Kawasaki diseaseChiea Chuen Khor, Sonia Davila, Willemijn B Breunis, et al.
Nature Genetics|October 18, 2011
Genome-wide association study identifies susceptibility loci for dengue shock syndrome at MICB and PLCE1Chiea Chuen Khor, Tran Nguyen Bich Chau, Junxiong Pang, et al.
Neurology|March 14, 2008
Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson diseaseK Haugarvoll, R Rademakers, J M Kachergus, et al.
Nature Medicine|November 18, 2023
The type II RAF inhibitor tovorafenib in relapsed/refractory pediatric low-grade glioma: the phase 2 FIREFLY-1 trialLindsay B Kilburn, Dong-Anh Khuong-Quang, Jordan R Hansford, et al.
The New England Journal of Medicine|October 23, 2009
Multicenter analysis of glucocerebrosidase mutations in Parkinson's diseaseE Sidransky, M A Nalls, J O Aasly, et al.
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