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Molecular Syndromology|October 27, 2016
Genetic Basis of Brain MalformationsElena Parrini, Valerio Conti, William B Dobyns, et al.
Journal of Theoretical Biology|November 25, 2010
A top-down linguistic approach to the analysis of genomic sequences: The metabotropic glutamate receptors 1 and 5 in human and in mouse as a case studyGiulia Menconi, Aldamaria Puliti, Isabella Sbrana, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 27, 2019
Lesional and non-lesional epilepsies: A blurring genetic boundaryRenzo Guerrini, Elena Parrini, Alessandro Esposito, et al.
Physiological Reviews|August 11, 2022
Developmental and epileptic encephalopathies: from genetic heterogeneity to phenotypic continuumRenzo Guerrini, Valerio Conti, Massimo Mantegazza, et al.
American Journal of Medical Genetics. Part A|January 5, 2011
Contractions in the second polyA tract of ARX are rare, non-pathogenic polymorphismsValerio Conti, Carla Marini, Davide Mei, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|October 28, 2020
Atypical Ocular Coloboma in Tuberous Sclerosis-2: Report of Two Novel CasesGiacomo M Bacci, Silvio Polizzi, Francesco Mari, et al.
American Journal of Medical Genetics. Part A|March 19, 2011
Corpus callosum agenesis, severe mental retardation, epilepsy, and dyskinetic quadriparesis due to a novel mutation in the homeodomain of ARXValerio Conti, Carla Marini, Simone Gana, et al.
Biochemical and Biophysical Research Communications|April 29, 2006
Expression of Tsga10 sperm tail protein in embryogenesis and neural development: from cilium to cell divisionBabak Behnam, Mohammad H Modarressi, Valerio Conti, et al.
Journal of Biophotonics|January 10, 2017
Multimodal fiber-probe spectroscopy allows detecting epileptogenic focal cortical dysplasia in childrenSuresh Anand, Riccardo Cicchi, Flavio Giordano, et al.
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