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Neurogenetics|October 18, 2016
Recurrent KIF2A mutations are responsible for classic lissencephalyMara Cavallin, Emilia K Bijlsma, Adrienne El Morjani, et al.
Nature Communications|October 13, 2025
Capturing disease severity in LIS1-lissencephaly reveals proteostasis dysregulation in patient-derived forebrain organoidsLea Zillich, Matteo Gasparotto, Andrea Carlo Rossetti, et al.
Brain : a Journal of Neurology|October 4, 2017
WDR81 mutations cause extreme microcephaly and impair mitotic progression in human fibroblasts and Drosophila neural stem cellsMara Cavallin, Maria A Rujano, Nathalie Bednarek, et al.
Neurology. Genetics|December 12, 2018
Delineating FOXG1 syndrome: From congenital microcephaly to hyperkinetic encephalopathyNancy Vegas, Mara Cavallin, Camille Maillard, et al.
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