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Neurology|October 19, 2012
PRRT2 mutations in familial infantile seizures, paroxysmal dyskinesia, and hemiplegic migraineCarla Marini, Valerio Conti, Davide Mei, et al.BMC Medical Genetics|March 4, 2014
Autism-epilepsy phenotype with macrocephaly suggests PTEN, but not GLIALCAM, genetic screeningMaria Marchese, Valerio Conti, Giulia Valvo, et al.International Journal of Molecular Sciences|December 11, 2025
SLC35A2-Related Brain Disorders: Genetics, Pathophysiology, and Therapeutic InsightsBeatrice Risso, Antonella Riva, Greta Volpedo, et al.Facial Plastic Surgery : FPS|April 26, 2021
Preliminary Functional Outcomes and Quality of Life after Tongue Reconstruction with the Vastus Lateralis Myofascial Free FlapArmando De Virgilio, Andrea Costantino, Raul Pellini, et al.European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|May 8, 2020
High definition three-dimensional exoscope (VITOM 3D) for microsurgery training: a preliminary experienceArmando De Virgilio, Andrea Costantino, Claudia Ebm, et al.Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|January 7, 2016
Computer-based automatic identification of neurons in gigavoxel-sized 3D human brain imagesPaolo Soda, Ludovica Acciai, Ermanno Cordelli, et al.Neurology. Genetics|February 5, 2021
Is Focal Cortical Dysplasia/Epilepsy Caused by Somatic MTOR Mutations Always a Unilateral Disorder?Renzo Guerrini, Mara Cavallin, Tommaso Pippucci, et al.International Journal of Molecular Medicine|September 12, 2006
crv4, a mouse model for human ataxia associated with kyphoscoliosis caused by an mRNA splicing mutation of the metabotropic glutamate receptor 1 (Grm1)Valerio Conti, Asadollah Aghaie, Michele Cilli, et al.Neuropharmacology|July 16, 2008
Presynaptic mGlu1 and mGlu5 autoreceptors facilitate glutamate exocytosis from mouse cortical nerve endingsVeronica Musante, Elisa Neri, Marco Feligioni, et al.Stem Cell Research|February 7, 2024
Generation of human induced pluripotent stem cell line (AOUMEYi001-A) from a patient affected by Congenital disorders of glycosylation (ALG8-CDG) using self-replicating RNA vectorRodolfo Tonin, Federica Feo, Silvia Falliano, et al.Pageof 7