| Actualities on molecular pathogenesis and repairing processes of cerebral damage in perinatal hypoxic-ischemic encephalopathy G Distefano, AD Praticò Italian Journal of pediatrics 36, 1-10, 2010 | 111 | 2010 |
| Ataxia in children: early recognition and clinical evaluation P Pavone, AD Praticò, V Pavone, R Lubrano, R Falsaperla, R Rizzo, ... Italian Journal of Pediatrics 43, 1-9, 2017 | 107 | 2017 |
| Congenital muscular dystrophy: from muscle to brain R Falsaperla, AD Praticò, M Ruggieri, E Parano, R Rizzo, G Corsello, ... Italian journal of pediatrics 42, 1-11, 2016 | 107 | 2016 |
| Hydranencephaly: cerebral spinal fluid instead of cerebral mantles P Pavone, AD Praticò, G Vitaliti, M Ruggieri, R Rizzo, E Parano, L Pavone, ... Italian journal of pediatrics 40, 1-8, 2014 | 104 | 2014 |
| Childhood neurofibromatosis type 2 (NF2) and related disorders: from bench to bedside and biologically targeted therapies M Ruggieri, AD Praticò, A Serra, L Maiolino, S Cocuzza, P Di Mauro, ... Acta Otorhinolaryngologica Italica 36 (5), 345, 2016 | 99 | 2016 |
| Mosaic neurocutaneous disorders and their causes M Ruggieri, AD Praticò Seminars in Pediatric Neurology 22 (4), 207-233, 2015 | 99 | 2015 |
| Off-label use of drugs and adverse drug reactions in pediatric units: a prospective, multicenter study AD Pratico, L Longo, S Mansueto, L Gozzo, I Barberi, V Tiralongo, V Salvo, ... Current drug safety 13 (3), 200-207, 2018 | 91 | 2018 |
| A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment P Pavone, AD Praticò, R Rizzo, G Corsello, M Ruggieri, E Parano, ... Medicine 96 (26), e6814, 2017 | 79 | 2017 |
| Diagnosis, management, and new therapeutic options in childhood neurofibromatosis type 2 and related forms M Ruggieri, AD Praticò, DG Evans Seminars in pediatric neurology 22 (4), 240-258, 2015 | 79 | 2015 |
| In vitro efficacy of ARQ 092, an allosteric AKT inhibitor, on primary fibroblast cells derived from patients with PIK3CA-related overgrowth spectrum (PROS) C Ranieri, S Di Tommaso, DC Loconte, V Grossi, P Sanese, R Bagnulo, ... Neurogenetics 19, 77-91, 2018 | 77 | 2018 |
| Hepatitis B vaccine in celiac disease: yesterday, today and tomorrow G Vitaliti, AD Praticò, C Cimino, G Di Dio, E Lionetti, M La Rosa, ... World Journal of Gastroenterology: WJG 19 (6), 838, 2013 | 72 | 2013 |
| Early history of the different forms of neurofibromatosis from ancient Egypt to the British Empire and beyond: first descriptions, medical curiosities, misconceptions … M Ruggieri, AD Praticò, R Caltabiano, A Polizzi American Journal of Medical Genetics Part A 176 (3), 515-550, 2018 | 70 | 2018 |
| The immunopathogenesis of cow’s milk protein allergy (CMPA) G Vitaliti, C Cimino, A Coco, AD Praticò, E Lionetti Italian journal of pediatrics 38, 1-5, 2012 | 66 | 2012 |
| Ketogenic diet for infants with epilepsy: a literature review R Falsaperla, G D'Angelo, AD Praticò, L Mauceri, M Barbagallo, P Pavone, ... Epilepsy & behavior 112, 107361, 2020 | 62 | 2020 |
| Congenital generalized hypertrichosis: the skin as a clue to complex malformation syndromes P Pavone, AD Praticò, R Falsaperla, M Ruggieri, M Zollino, G Corsello, ... Italian Journal of Pediatrics 41, 1-8, 2015 | 62 | 2015 |
| Neurofibromatosis type 1 and infantile spasms M Ruggieri, P Iannetti, M Clementi, A Polizzi, G Incorpora, A Spalice, ... Child's Nervous System 25, 211-216, 2009 | 61 | 2009 |
| A mosaic pattern of INI1/SMARCB1 protein expression distinguishes Schwannomatosis and NF2-associated peripheral schwannomas from solitary peripheral schwannomas and NF2 … R Caltabiano, G Magro, A Polizzi, AD Praticò, A Ortensi, V D’Orazi, ... Child's Nervous System 33, 933-940, 2017 | 56 | 2017 |
| Primary headaches in children: clinical findings and the association with other conditions P Pavone, R Rizzo, I Conti, A Verrotti, A Mistretta, R Falsaperla, ... International journal of immunopathology and pharmacology 25 (4), 1083-1091, 2012 | 56 | 2012 |
| Hypomelanosis of Ito: a round on the frequency and type of epileptic complications P Pavone, AD Praticò, M Ruggieri, R Falsaperla Neurological Sciences 36, 1173-1180, 2015 | 55 | 2015 |
| Wide spectrum of congenital anomalies including choanal atresia, malformed extremities, and brain and spinal malformations in a girl with a de novo 5.6‐Mb deletion of 13q12. 11 … P Pavone, S Briuglia, R Falsaperla, A Warm, V Pavone, L Bernardini, ... American Journal of Medical Genetics Part A 164 (7), 1734-1743, 2014 | 55 | 2014 |
salvatore leonardiDepartment of Pediatrics. University of Catania在 unict.it 的电子邮件经过验证
salvatore leonardiDepartment of Pediatrics. University of Catania在 unict.it 的电子邮件经过验证