| Inflammatory bowel disease: genetics, epigenetics, and pathogenesis I Loddo, C Romano Frontiers in immunology 6, 159896, 2015 | 494 | 2015 |
| Partially hydrolyzed guar gum in pediatric functional abdominal pain C Romano, D Comito, A Famiani, S Calamarà, I Loddo World Journal of Gastroenterology: WJG 19 (2), 235, 2013 | 74 | 2013 |
| Incidence of hypocalcemia and hypercalcemia in hospitalized patients: Is it changing? A Catalano, D Chilà, F Bellone, G Nicocia, G Martino, I Loddo, N Morabito, ... Journal of clinical & translational endocrinology 13, 9-13, 2018 | 60 | 2018 |
| Exploring by whole exome sequencing patients with initial diagnosis of Rubinstein–Taybi syndrome: the interconnections of epigenetic machinery disorders G Negri, P Magini, D Milani, M Crippa, E Biamino, M Piccione, S Sotgiu, ... Human Genetics 138, 257-269, 2019 | 35 | 2019 |
| Proton pump inhibitors in pediatrics: evaluation of efficacy in GERD therapy C Romano, A Chiaro, D Comito, I Loddo, V Ferrau Current Clinical Pharmacology 6 (1), 41-47, 2011 | 32 | 2011 |
| Nonalcoholic Fatty liver disease/non-alcoholic steatohepatitis in childhood: endocrine-metabolic “mal-programming” S Manti, C Romano, V Chirico, M Filippelli, C Cuppari, I Loddo, ... Hepatitis Monthly 14 (5), 2014 | 23 | 2014 |
| New patients with Temple syndrome caused by 14q32 deletion: Genotype‐phenotype correlations and risk of thyroid cancer G Severi, L Bernardini, S Briuglia, S Bigoni, B Buldrini, P Magini, ... American Journal of Medical Genetics Part A 170 (1), 162-169, 2016 | 21 | 2016 |
| Autoimmune liver disease in Noonan Syndrome I Loddo, C Romano, MC Cutrupi, M Sciveres, S Riva, A Salpietro, ... European Journal of Medical Genetics 58 (3), 188-190, 2015 | 18 | 2015 |
| A de novo 0.63 Mb 6q25. 1 deletion associated with growth failure, congenital heart defect, underdeveloped cerebellar vermis, abnormal cutaneous elasticity and joint laxity V Salpietro, M Ruggieri, K Mankad, G Di Rosa, F Granata, I Loddo, ... American Journal of Medical Genetics Part A 167 (9), 2042-2051, 2015 | 14 | 2015 |
| LMNA gene mutation as a model of cardiometabolic dysfunction: from genetic analysis to treatment response V Chirico, V Ferraù, I Loddo, S Briuglia, M Amorini, V Salpietro, ... Diabetes & metabolism 40 (3), 224-228, 2014 | 12 | 2014 |
| Inflammatory bowel disease: Genetics, epigenetics, and pathogenesis. Front Immunol. 2015; 6: 551 I Loddo, C Romano | 10 | 2015 |
| How do cardiologists select patients for dual antiplatelet therapy continuation beyond 1 year after a myocardial infarction? Insights from the EYESHOT Post‐MI Study L De Luca, F Colivicchi, J Meessen, M Uguccioni, F Piscione, P Bernabò, ... Clinical Cardiology 42 (11), 1113-1120, 2019 | 7 | 2019 |
| Genetics and cardiovascular disease I Loddo, F Barbera, G Di Gesaro, MC Cutrupi, MP Calabrò, G Ceravolo, ... Journal of biological regulators and homeostatic agents 34 (4 Suppl. 2), 17, 2020 | 6 | 2020 |
| Eosinophilic esophagitis in children: current knowledge to open new horizons: Eosinophilic esophagitis in pediatrics T Alterio, S Cardile, C Trayers, S Valenti, I Loddo, R Mardare, A Mosca, ... Scandinavian Journal of Gastroenterology 54 (7), 822-829, 2019 | 6 | 2019 |
| Cardiac defects in RASopathies: a review of genotype-phenotype correlations I Loddo, MC Cutrupi, D Concolino, R De Sarro, A Barbalace, A Salpietro, ... Journal of biological regulators and homeostatic agents 34 (4 Suppl. 2), 23, 2020 | 4 | 2020 |
| Impact of measurement of infliximab and anti-infliximab antibodies levels in pediatric inflammatory bowel disease S Cardile, A Costa, I Loddo, G Morabito, C Pidone, C Romano Digestive and Liver Disease 45, e294-e295, 2013 | 3 | 2013 |
| Pseudotumor cerebri e Papilledema Idiopatico: un'analisi retrospettiva di tre centri pediatrici italiani. V SALPIETRO DAMIANO, AC Romeo, K Mankad, A Adams, M Valenzise, ... RIVISTA ITALIANA DI GENETICA E IMMUNOLOGIA PEDIATRICA 4 (1), 1-9, 2013 | 1 | 2013 |
| Familial Mediterranean Fever: an overview R Gallizzi, P Vicchio, I Loddo The child: a journal of pediatrics 1 (1), 2012 | 1 | 2012 |
| Deficit di sottoclassi di IgG: tra storia e attualità A Salpietro, GE Calabrò, I Loddo, L Colavita, L Grasso, P Vicchio, ... Rivista Italiana di Genetica e Immunologia Pediatrica 1, 5-5, 2009 | 1 | 2009 |
| Markers di stress ossidativo in bambini con Sindrome di Down S Briuglia, C Cuppari, D Comito, B Russo, R Caruso, I Loddo, L Melcarne, ... | 1 | 2009 |
