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Annals of Clinical and Translational Neurology|March 27, 2019
Contribution of ultrarare variants in mTOR pathway genes to sporadic focal epilepsiesTommaso Pippucci, Laura Licchetta, Sara Baldassari, et al.
Disability and Rehabilitation|May 19, 2021
Challenges and resources in adult life with Joubert syndrome: issues from an international classification of functioning (ICF) perspectiveRomina Romaniello, Chiara Gagliardi, Patrizia Desalvo, et al.
Annals of Neurology|March 30, 2004
Benign familial neonatal-infantile seizures: characterization of a new sodium channelopathySamuel F Berkovic, Sarah E Heron, Lucio Giordano, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 3, 2020
Posterior Reversible Encephalopathy Syndrome in infants and young childrenDuccio Maria Cordelli, Chiara Marra, Lara Ciampoli, et al.
Epilepsy Research|November 7, 2016
Epilepsy in ring chromosome 20 syndromeAglaia Vignoli, Francesca Bisulli, Francesca Darra, et al.
The Journal of Pediatrics|September 3, 2013
Electroclinical features and long-term outcome of cryptogenic epilepsy in children with Down syndromeAlberto Verrotti, Raffaella Cusmai, Francesco Nicita, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 8, 2018
Impaired urinary concentration ability is a sensitive predictor of renal disease progression in Joubert syndromeSara Nuovo, Laura Fuiano, Alessia Micalizzi, et al.
International Journal of Legal Medicine|August 15, 2014
Genetic and forensic implications in epilepsy and cardiac arrhythmias: a case seriesSara Partemi, Monica Coll Vidal, Pasquale Striano, et al.
Neonatology|October 26, 2023
External Validation of a Multivariate Model for Targeted Surfactant ReplacementFrancesco Raimondi, Pasquale Dolce, Claudio Veropalumbo, et al.
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