| Attention deficit and hyperactivity disorders in the offspring of mothers exposed to mild-moderate iodine deficiency: a possible novel iodine deficiency disorder in developed … F Vermiglio, VP Lo Presti, M Moleti, M Sidoti, G Tortorella, G Scaffidi, ... The Journal of Clinical Endocrinology & Metabolism 89 (12), 6054-6060, 2004 | 610 | 2004 |
| Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation A Guilmatre, C Dubourg, AL Mosca, S Legallic, A Goldenberg, ... Archives of general psychiatry 66 (9), 947-956, 2009 | 542 | 2009 |
| Congenital muscular dystrophies with defective glycosylation of dystroglycan: a population study E Mercuri, S Messina, C Bruno, M Mora, E Pegoraro, GP Comi, A D'Amico, ... Neurology 72 (21), 1802-1809, 2009 | 202 | 2009 |
| Topiramate as add-on drug in severe myoclonic epilepsy in infancy: an Italian multicenter open trial G Coppola, G Capovilla, A Montagnini, A Romeo, M Spanò, G Tortorella, ... Epilepsy research 49 (1), 45-48, 2002 | 157 | 2002 |
| PRRT2 mutations in familial infantile seizures, paroxysmal dyskinesia, and hemiplegic migraine C Marini, V Conti, D Mei, D Battaglia, D Lettori, E Losito, G Bruccini, ... Neurology 79 (21), 2109-2114, 2012 | 135 | 2012 |
| Ictal and interictal EEG abnormalities in ADHD children recorded over night by video-polysomnography R Silvestri, A Gagliano, T Calarese, I Arico, C Cedro, R Condurso, ... Epilepsy research 75 (2-3), 130-137, 2007 | 121 | 2007 |
| Description, nomenclature, and mapping of a novel cerebello-renal syndrome with the molar tooth malformation EM Valente, DC Salpietro, F Brancati, E Bertini, T Galluccio, G Tortorella, ... The American Journal of Human Genetics 73 (3), 663-670, 2003 | 113 | 2003 |
| Novel TMEM67 mutations and genotype‐phenotype correlates in meckelin‐related ciliopathies M Iannicelli, F Brancati, S Mougou‐Zerelli, A Mazzotta, S Thomas, ... Human mutation 31 (5), E1319-E1331, 2010 | 112 | 2010 |
| Bilateral occipital calcification, epilepsy and coeliac disease: clinical and neuroimaging features of a new syndrome. A Magaudda, B Dalla Bernardina, P De Marco, Z Sfaello, M Longo, ... Journal of Neurology, Neurosurgery & Psychiatry 56 (8), 885-889, 1993 | 104 | 1993 |
| Familial periventricular heterotopia: Missense and distal truncating mutations of the FLN1 gene F Moro, R Carrozzo, P Veggiotti, G Tortorella, D Toniolo, A Volzone, ... Neurology 58 (6), 916-921, 2002 | 96 | 2002 |
| Cognitive training modifies frequency EEG bands and neuropsychological measures in Rett syndrome RA Fabio, L Billeci, G Crifaci, E Troise, G Tortorella, G Pioggia Research in developmental disabilities 53, 73-85, 2016 | 84 | 2016 |
| Levetiracetam during 1-year follow-up in children, adolescents, and young adults with refractory epilepsy G Coppola, S Mangano, G Tortorella, A Pelliccia, A Fels, A Romano, ... Epilepsy research 59 (1), 35-42, 2004 | 76 | 2004 |
| Effects of maternal iodine nutrition and thyroid status on cognitive development in offspring: a pilot study M Moleti, F Trimarchi, G Tortorella, A Candia Longo, G Giorgianni, ... Thyroid 26 (2), 296-305, 2016 | 72 | 2016 |
| Topiramate as add-on drug in children, adolescents and young adults with Lennox-Gastaut syndrome: an Italian multicentric study G Coppola, G Caliendo, P Veggiotti, A Romeo, G Tortorella, P De Marco, ... Epilepsy research 51 (1-2), 147-153, 2002 | 71 | 2002 |
| Nonsyndromic mental retardation and cryptogenic epilepsy in women with Doublecortin gene mutations R Guerrini, F Moro, E Andermann, E Hughes, D D'Agostino, R Carrozzo, ... Annals of neurology 54 (1), 30-37, 2003 | 66 | 2003 |
| Mutational Analysis of EFHC1 Gene in Italian Families with Juvenile Myoclonic Epilepsy F Annesi, A Gambardella, R Michelucci, A Bianchi, C Marini, MP Canevini, ... Epilepsia 48 (9), 1686-1690, 2007 | 62 | 2007 |
| Efficacy of folic acid in children with migraine, hyperhomocysteinemia and MTHFR polymorphisms G Di Rosa, S Attinà, M Spanò, G Ingegneri, DL Sgrò, G Pustorino, ... Headache: The Journal of Head and Face Pain 47 (9), 1342-1344, 2007 | 61 | 2007 |
| Pediatric idiopathic intracranial hypertension and the underlying endocrine-metabolic dysfunction: a pilot study V Salpietro, K Mankad, M Kinali, A Adams, M Valenzise, G Tortorella, ... Journal of Pediatric Endocrinology and Metabolism 27 (1-2), 107-115, 2014 | 58 | 2014 |
| Epileptic disorders with onset in the first year of life: neurological and cognitive outcome D Battaglia, T Rando, F Deodato, G Bruccini, G Baglio, MF Frisone, ... European Journal of Paediatric Neurology 3 (3), 95-103, 1999 | 58 | 1999 |
| A novel CDKL5 mutation in a 47,XXY boy with the early‐onset seizure variant of Rett syndrome S Sartori, G Di Rosa, R Polli, E Bettella, G Tricomi, G Tortorella, A Murgia American Journal of Medical Genetics Part A 149 (2), 232-236, 2009 | 55 | 2009 |
