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Neuropsychiatric Disease and Treatment|November 10, 2009
Psychological and behavioral disease during developmental age: the importance of the alliance with parentsMichela Gatta, Elisabetta Ramaglioni, Jessica Lai, et al.
Human Mutation|February 28, 2007
Argininosuccinate lyase deficiency: mutational spectrum in Italian patients and identification of a novel ASL pseudogeneEva Trevisson, Leonardo Salviati, Maria Cristina Baldoin, et al.
Neuroradiology|August 6, 2013
Secondary parenchymal and vascular changes after middle cerebral artery stroke in childrenRenzo Manara, Stefano Sartori, Margherita Nosadini, et al.
Life (Basel, Switzerland)|August 28, 2025
Nighttime Primary Headaches in Children: Beyond Hypnic Headache, a Comprehensive ReviewBeatrice Baldo, Ilaria Bonemazzi, Antonella Morea, et al.
Brain & Development|July 11, 2013
14q12 duplication including FOXG1: is there a common age-dependent epileptic phenotype?Chiara Bertossi, Matteo Cassina, Luca De Palma, et al.
Pediatric Neurology|October 11, 2024
Cortical Gyrification Is Associated With the Clinical Phenotype in Tuberous Sclerosis ComplexNicolò Trevisan, Francesco Brunello, Fabio Sambataro, et al.
Developmental Medicine and Child Neurology|October 10, 2018
Tuberous sclerosis-associated neuropsychiatric disorders: a paediatric cohort studyIrene Toldo, Valeria Brasson, Marina Miscioscia, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 4, 2026
A rare complication of vagus nerve stimulation surgery: the Horner Syndrome. Case report and systematic reviewGiulia M Furlanis, Gabriele Scarselletti, Jacopo Favaro, et al.
Neuroimage|July 3, 2023
The maturation of aperiodic EEG activity across development reveals a progressive differentiation of wakefulness from sleepJacopo Favaro, Michele Angelo Colombo, Ezequiel Mikulan, et al.
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