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Epileptic Disorders : International Epilepsy Journal with Videotape|May 26, 2007
Genetics of epilepsy: epilepsy research foundation workshop reportSanjay Sisodiya, J Helen Cross, Ingmar Blümcke, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|January 15, 2021
Five-Year Outcomes From the Randomized, Phase III Trials CheckMate 017 and 057: Nivolumab Versus Docetaxel in Previously Treated Non-Small-Cell Lung CancerHossein Borghaei, Scott Gettinger, Everett E Vokes, et al.
Journal of Neurodevelopmental Disorders|January 15, 2022
Down-regulation of the brain-specific cell-adhesion molecule contactin-3 in tuberous sclerosis complex during the early postnatal periodAnatoly Korotkov, Mark J Luinenburg, Alessia Romagnolo, et al.
Human Molecular Genetics|September 5, 2001
Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in femalesV L Sheen, P H Dixon, J W Fox, et al.
Brain : a Journal of Neurology|June 14, 2015
Recessive nephrocerebellar syndrome on the Galloway-Mowat syndrome spectrum is caused by homozygous protein-truncating mutations of WDR73Robert N Jinks, Erik G Puffenberger, Emma Baple, et al.
Neuropathology and Applied Neurobiology|May 4, 2021
MicroRNA-34a activation in tuberous sclerosis complex during early brain development may lead to impaired corticogenesisAnatoly Korotkov, Nam Suk Sim, Mark J Luinenburg, et al.
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