Alberto Spalice | Ricerc@Sapienza

Pubblicazioni

Titolo	Pubblicato in	Anno
The possible use of the L-type calcium channel antagonist verapamil in drug-resistant epilepsy	EXPERT REVIEW OF NEUROTHERAPEUTICS	2016
Clinical dissection of childhood occipital epilepsy of Gastaut and prognostic implication	EUROPEAN JOURNAL OF NEUROLOGY	2016
Epilepsy is a possible feature in Williams-Beuren syndrome patients harboring typical deletions of the 7q11.23 critical region	AMERICAN JOURNAL OF MEDICAL GENETICS. PART A	2016
Mean platelet volume, Vitamin D and C reactive protein levels in normal weight children with primary snoring and obstructive sleep apnea syndrome	PLOS ONE	2016
Effectiveness and tolerability of perampanel in children and adolescents with refractory epilepsies-An Italian observational multicenter study	EPILEPSY RESEARCH	2016
Epilepsy in the setting of full trisomy 18. A multicenter study on 18 affected children with and without structural brain abnormalities	AMERICAN JOURNAL OF MEDICAL GENETICS. PART C, SEMINARS IN MEDICAL GENETICS	2016
The crucial role of FBXO28 in the pathogenesis of the 1q41q42 microdeletion syndrome	AMERICAN JOURNAL OF MEDICAL GENETICS. PART A	2016
Stroke and migraine is there a possible comorbidity?	THE ITALIAN JOURNAL OF PEDIATRICS	2016
Severe early onset ethylmalonic encephalopathy with west syndrome	METABOLIC BRAIN DISEASE	2015
Refractory absence seizures. An Italian multicenter retrospective study	EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY	2015
Myoclonic status and central fever in Angelman syndrome due to paternal uniparental disomy	JOURNAL OF NEUROGENETICS	2015
Early myoclonic encephalopathy in 9q33-q34 deletion encompassing STXBP1 and SPTAN1	ANNALS OF HUMAN GENETICS	2015