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Journal of the National Cancer Institute|February 1, 2023
Recommendations for Epstein-Barr virus-based screening for nasopharyngeal cancer in high- and intermediate-risk regionsW K Jacky Lam, Ann D King, Jacob A Miller, et al.Plos One|May 22, 2015
Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF RegistryLouis Viollet, Gustavo Glusman, Kelley J Murphy, et al.Vaccines|May 28, 2022
A SARS-CoV-2 Spike Ferritin Nanoparticle Vaccine Is Protective and Promotes a Strong Immunological Response in the Cynomolgus Macaque Coronavirus Disease 2019 (COVID-19) ModelSara C Johnston, Keersten M Ricks, Ines Lakhal-Naouar, et al.Nature Genetics|July 31, 2012
De novo mutations in ATP1A3 cause alternating hemiplegia of childhoodErin L Heinzen, Kathryn J Swoboda, Yuki Hitomi, et al.Nature Genetics|November 18, 2014
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsyMikko Muona, Samuel F Berkovic, Leanne M Dibbens, et al.Nature Communications|February 19, 2021
Scaling advantage over path-integral Monte Carlo in quantum simulation of geometrically frustrated magnetsAndrew D King, Jack Raymond, Trevor Lanting, et al.JAMA Oncology|October 10, 2024
Ninth Version of the AJCC and UICC Nasopharyngeal Cancer TNM Staging ClassificationJian-Ji Pan, Hai-Qiang Mai, Wai Tong Ng, et al.Brain : a Journal of Neurology|November 21, 2013
Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2A Reghan Foley, Manoj P Menezes, Amelie Pandraud, et al.Neurology|October 28, 2022
Neurodevelopmental and Epilepsy Phenotypes in Individuals With Missense Variants in the Voltage-Sensing and Pore Domains of KCNH5Hannah C Happ, Lynette G Sadleir, Matthew Zemel, et al.Human Mutation|January 7, 2010
An overview of L-2-hydroxyglutarate dehydrogenase gene (L2HGDH) variants: a genotype-phenotype studyMarjan E Steenweg, Cornelis Jakobs, Abdellatif Errami, et al.Pageof 214