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Scientific Reports|July 8, 2025
MAN2A2-related glycosylation defects in autism and cognitive delaySimone Treccarichi, Mirella Vinci, Lara Cirnigliaro, et al.
Neuromolecular Medicine|September 21, 2023
Fibroblast Growth Factor Receptor 2 (FGFR2), a New Gene Involved in the Genesis of Autism Spectrum DisorderAntonio Gennaro Nicotera, Greta Amore, Maria Concetta Saia, et al.
Medicina (Kaunas, Lithuania)|April 26, 2025
Investigating the Role of the Zinc Finger Protein ZC2HC1C on Autism Spectrum Disorder SusceptibilitySimone Treccarichi, Mirella Vinci, Antonino Musumeci, et al.
Molecular Cytogenetics|January 18, 2013
6p22.3 deletion: report of a patient with autism, severe intellectual disability and electroencephalographic anomaliesDaniela Di Benedetto, Giuseppa Di Vita, Corrado Romano, et al.
Gene|September 16, 2024
PPP2R5E: New gene potentially involved in specific learning disorders and myopathyAntonino Musumeci, Mirella Vinci, Iris Verbinnen, et al.
European Journal of Human Genetics : EJHG|January 27, 2019
Multiple genomic copy number variants associated with periventricular nodular heterotopia indicate extreme genetic heterogeneityElena Cellini, Annalisa Vetro, Valerio Conti, et al.
Journal of Autism and Developmental Disorders|February 7, 2019
EEG Abnormalities as a Neurophysiological Biomarker of Severity in Autism Spectrum Disorder: A Pilot Cohort StudyAntonio Gennaro Nicotera, Randi Jenssen Hagerman, Maria Vincenza Catania, et al.
Genes|August 29, 2024
PLEKHG1: New Potential Candidate Gene for Periventricular White Matter AbnormalitiesFrancesco Calì, Mirella Vinci, Simone Treccarichi, et al.
Journal of Molecular Neuroscience : MN|June 11, 2026
A de novo Loss-of-function Variant in RAPGEF6 Supports its Role in Neuropsychiatric DisordersSimone Treccarichi, Mirella Vinci, Maria Grazia Figura, et al.
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