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The Lancet. Neurology|April 5, 2011
Clinical, environmental, and genetic determinants of multiple sclerosis in children with acute demyelination: a prospective national cohort studyBrenda Banwell, Amit Bar-Or, Douglas L Arnold, et al.Nature Genetics|November 26, 2008
Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalitiesNicola Brunetti-Pierri, Jonathan S Berg, Fernando Scaglia, et al.Neurology|May 11, 2016
Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathyJohannes R Lemke, Kirsten Geider, Katherine L Helbig, et al.Brain : a Journal of Neurology|January 23, 2019
PLPHP deficiency: clinical, genetic, biochemical, and mechanistic insightsDevon L Johnstone, Hilal H Al-Shekaili, Maja Tarailo-Graovac, et al.Nature Communications|June 18, 2020
Recurrent horizontal transfer identifies mitochondrial positive selection in a transmissible cancerAndrea Strakova, Thomas J Nicholls, Adrian Baez-Ortega, et al.Physical Review Letters|February 15, 2001
Elliptic flow in Au+Au collisions at square root(S)NN = 130 GeVK H Ackermann, N Adams, C Adler, et al.Pageof 138