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Neurology. Genetics|April 24, 2023
Neurologic, Neuropsychologic, and Neuroradiologic Features of EBF3-Related SyndromeClaudia Ciaccio, Chiara Pantaleoni, Marco Moscatelli, et al.Neuropathology and Applied Neurobiology|July 10, 2026
Papillary Tumour of the Pineal Region, in a Child With a Germline PTEN Pathogenic Variant, Arisen in the Fourth VentricleGianluca Marucci, Veronica Saletti, Rosina Paterra, et al.Neuropsychologia|May 3, 2015
Time, number and attention in very low birth weight childrenFrancesca Tinelli, Giovanni Anobile, Monica Gori, et al.European Journal of Cancer Care|January 7, 2020
Motherhood during or after breast cancer diagnosis: A qualitative studyFlavia Faccio, Eleonora Mascheroni, Chiara Ionio, et al.Developmental Medicine and Child Neurology|April 11, 2016
Patient-reported outcomes measure for children born preterm: validation of the SOLE VLBWI Questionnaire, a new quality of life self-assessment toolIvana Olivieri, Stefania M Bova, Elisa Fazzi, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 3, 2010
Language abilities and gestural communication in a girl with bilateral perisylvian syndrome: a clinical and rehabilitative follow-upBruna Molteni, Daniela Sarti, Gloria Airaghi, et al.Disability and Rehabilitation|December 9, 2009
Use of ICF to describe functioning and disability in children with brain tumoursDaniela Ajovalasit, Chiara Vago, Arianna Usilla, et al.American Journal of Medical Genetics. Part A|September 27, 2014
Seizures and EEG features in 74 patients with genetic-dysmorphic syndromesEnrico Alfei, Federico Raviglione, Silvana Franceschetti, et al.Journal of Neurology|February 17, 2010
Identification of previously unreported mutations in CHRNA1, CHRNE and RAPSN genes in three unrelated Italian patients with congenital myasthenic syndromesRaffaella Brugnoni, Lorenzo Maggi, Eleonora Canioni, et al.Molecular Genetics & Genomic Medicine|January 8, 2016
126 novel mutations in Italian patients with neurofibromatosis type 1Donatella Bianchessi, Sara Morosini, Veronica Saletti, et al.Pageof 17