Showing results (1411-1420 of 1,434) with videos related to
Sort By:
Pageof 144
International Journal of Stroke : Official Journal of the International Stroke Society|July 20, 2010
Stroke: working toward a prioritized world agendaVladimir Hachinski, Geoffrey A Donnan, Philip B Gorelick, et al.Stroke|May 26, 2010
Stroke: working toward a prioritized world agendaVladimir Hachinski, Geoffrey A Donnan, Philip B Gorelick, et al.The Journal of Clinical Investigation|May 27, 2021
Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19Gundula Povysil, Guillaume Butler-Laporte, Ning Shang, et al.American Journal of Human Genetics|April 20, 2010
Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromesErin L Heinzen, Rodney A Radtke, Thomas J Urban, et al.Epilepsia|May 27, 2021
CSNK2B: A broad spectrum of neurodevelopmental disability and epilepsy severityMichelle E Ernst, Evan H Baugh, Amanda Thomas, et al.Human Molecular Genetics|February 2, 2013
A genome-wide association study of resistance to HIV infection in highly exposed uninfected individuals with hemophilia AJérôme Lane, Paul J McLaren, Lucy Dorrell, et al.Annals of Neurology|October 1, 2018
NBEA: Developmental disease gene with early generalized epilepsy phenotypesMaureen S Mulhern, Constance Stumpel, Nicholas Stong, et al.The EMBO Journal|November 14, 2018
Loss of tubulin deglutamylase CCP1 causes infantile-onset neurodegenerationVandana Shashi, Maria M Magiera, Dennis Klein, et al.Nature|August 1, 2008
Large recurrent microdeletions associated with schizophreniaHreinn Stefansson, Dan Rujescu, Sven Cichon, et al.Nature|August 2, 2023
Africa-specific human genetic variation near CHD1L associates with HIV-1 loadPaul J McLaren, Immacolata Porreca, Gennaro Iaconis, et al.Pageof 144