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Journal of Medical Genetics|September 1, 1993
Uniparental disomy explains the occurrence of the Angelman or Prader-Willi syndrome in patients with an additional small inv dup(15) chromosomeW P Robinson, J Wagstaff, F Bernasconi, et al.
Seizure|May 25, 2005
Efficacy and safety of levetiracetam: an add-on trial in children with refractory epilepsyS Grosso, E Franzoni, G Coppola, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 27, 2018
Neuropsychological profile in Italian children with neurofibromatosis type 1 (NF1) and their relationships with neuroradiological data: Preliminary resultsA Parmeggiani, F Boiani, S Capponi, et al.
The Neuroradiology Journal|September 25, 2013
MRI Findings in Patients with Clinical Onset Consistent with Infantile Neuroaxonal Dystrophy (INAD), Literature Review, Clinical and MRI Follow-upB Bernardi, A Pini, M Santucci, et al.
American Journal of Medical Genetics|July 12, 1996
X-linked neurodegenerative syndrome with congenital ataxia, late-onset progressive myoclonic encephalopathy and selective macular degeneration, linked to Xp22.33-pterV des Portes, L Bachner, T Brüls, et al.
European Journal of Neurology|July 30, 2010
Rufinamide in refractory childhood epileptic encephalopathies other than Lennox-Gastaut syndromeG Coppola, S Grosso, E Franzoni, et al.
Eating and Weight Disorders : EWD|October 27, 2010
[Obesity and Eating Disorders. Indications for the different levels of care. An Italian Expert Consensus Document]L M Donini, M Cuzzolaro, G Spera, et al.
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