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Annals of Neurology|February 2, 2006
UCHL-1 is not a Parkinson's disease susceptibility geneDaniel G Healy, Patrick M Abou-Sleiman, Juan P Casas, et al.Brain Communications|August 16, 2021
Alternating hemiplegia of childhood: evolution over time and mouse model corroborationJulie Uchitel, Keri Wallace, Linh Tran, et al.Science (New York, N.Y.)|February 3, 2022
A highly virulent variant of HIV-1 circulating in the NetherlandsChris Wymant, Daniela Bezemer, François Blanquart, et al.BMJ Open|December 26, 2024
Paediatric Personalized Research Network Switzerland (SwissPedHealth): a joint paediatric national data streamRebeca Mozun, Fabiën N Belle, Andrea Agostini, et al.Nature Metabolism|March 24, 2021
Serine biosynthesis defect due to haploinsufficiency of PHGDH causes retinal diseaseKevin Eade, Marin L Gantner, Joseph A Hostyk, et al.Nature Neuroscience|June 29, 2021
Exome sequencing in obsessive-compulsive disorder reveals a burden of rare damaging coding variantsMathew Halvorsen, Jack Samuels, Ying Wang, et al.Annals of Neurology|December 19, 2022
Rare Genetic Variation and Outcome of Surgery for Mesial Temporal Lobe EpilepsyPiero Perucca, Kate Stanley, Natasha Harris, et al.Gastroenterology|July 20, 2010
A polymorphism near IL28B is associated with spontaneous clearance of acute hepatitis C virus and jaundiceHans L Tillmann, Alex J Thompson, Keyur Patel, et al.Journal of the American Society of Nephrology : JASN|May 16, 2019
Exome-Based Rare-Variant Analyses in CKDSophia Cameron-Christie, Charles J Wolock, Emily Groopman, et al.Epilepsia|April 18, 2007
A multicenter study of BRD2 as a risk factor for juvenile myoclonic epilepsyGianpiero L Cavalleri, Nicole M Walley, Nicole Soranzo, et al.Pageof 51