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Epilepsia|October 9, 2013
Early onset absence epilepsy with onset in the first year of life: a multicenter cohort studyLucio Giordano, Aglaia Vignoli, Raffaella Cusmai, et al.
Orphanet Journal of Rare Diseases|June 10, 2011
Pontine Tegmental Cap Dysplasia: developmental and cognitive outcome in three adolescent patientsMarilena Briguglio, Lorenzo Pinelli, Lucio Giordano, et al.
American Journal of Medical Genetics. Part A|May 14, 2011
Clinical and molecular description of a Wilms tumor in a patient with tuberous sclerosis complexFilippo Spreafico, Lucia Dora Notarangelo, Richard Fabian Schumacher, et al.
Epilepsy & Behavior : E&B|August 24, 2010
Epilepsy in Rett syndrome: clinical and genetic featuresMaria Pintaudi, Maria Grazia Calevo, Aglaia Vignoli, et al.
BMC Medical Genetics|October 14, 2010
Genetic investigations on 8 patients affected by ring 20 chromosome syndromeDaniela Giardino, Aglaia Vignoli, Lucia Ballarati, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 3, 2012
Seizures and EEG patterns in Pallister-Killian syndrome: 13 new Italian patientsLucio Giordano, Maurizio Viri, Renato Borgatti, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 10, 2018
Long-term follow-up in pediatric patients with paroxysmal hypothermia (Shapiro's syndrome)Nicola Tambasco, Federico Paolini Paoletti, Giulia Prato, et al.
Cell and Tissue Research|March 19, 2024
Joubert syndrome-derived induced pluripotent stem cells show altered neuronal differentiation in vitroRoberta De Mori, Silvia Tardivo, Lidia Pollara, et al.
Frontiers in Neurology|January 3, 2022
Sleep in Children With Pallister Killian Syndrome: A Prospective Clinical and Videopolysomnographic StudyAnna Fetta, Veronica Di Pisa, Martina Ruscelli, et al.
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