| Expert consensus document: Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: an international consensus statement. F Brioude, JM Kalish, A Mussa, AC Foster, J Bliek, GB Ferrero, ... Nat Rev Endocrinol 14 (4), 229-249, 2018 | 484* | 2018 |
| Thyroid nodules and cancer in children and adolescents affected by autoimmune thyroiditis A Corrias, A Cassio, G Weber, A Mussa, M Wasniewska, A Rapa, ... Archives of pediatrics & adolescent medicine 162 (6), 526-531, 2008 | 216 | 2008 |
| Diagnostic features of thyroid nodules in pediatrics A Corrias, A Mussa, F Baronio, T Arrigo, M Salerno, M Segni, MC Vigone, ... Archives of pediatrics & adolescent medicine 164 (8), 714-719, 2010 | 165 | 2010 |
| Prospective evaluation of the natural course of idiopathic subclinical hypothyroidism in childhood and adolescence M Wasniewska, M Salerno, A Cassio, A Corrias, T Aversa, G Zirilli, ... European Journal of Endocrinology 160 (3), 417-421, 2009 | 164 | 2009 |
| Cancer risk in Beckwith-Wiedemann syndrome: a systematic review and meta-analysis outlining a novel (Epi) genotype specific histotype targeted screening protocol A Mussa, C Molinatto, G Baldassarre, E Riberi, S Russo, L Larizza, ... The Journal of pediatrics 176, 142-149. e1, 2016 | 159 | 2016 |
| The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith–Wiedemann syndrome and Silver–Russell … N Chiesa, A De Crescenzo, K Mishra, L Perone, M Carella, O Palumbo, ... Human molecular genetics 21 (1), 10-25, 2012 | 144 | 2012 |
| Prevalence of Beckwith–Wiedemann syndrome in north west of Italy A Mussa, S Russo, A De Crescenzo, N Chiesa, C Molinatto, A Selicorni, ... American journal of medical genetics Part A 161 (10), 2481-2486, 2013 | 142 | 2013 |
| (Epi) genotype–phenotype correlations in Beckwith–Wiedemann syndrome A Mussa, S Russo, A De Crescenzo, A Freschi, L Calzari, S Maitz, ... European journal of human genetics 24 (2), 183-190, 2016 | 141 | 2016 |
| The natural history of the normal/mild elevated TSH serum levels in children and adolescents with Hashimoto’s thyroiditis and isolated hyperthyrotropinaemia: a 3‐year follow‐up G Radetti, M Maselli, F Buzi, A Corrias, A Mussa, P Cambiaso, M Salerno, ... Clinical endocrinology 76 (3), 394-398, 2012 | 136 | 2012 |
| Assisted reproductive techniques and risk of Beckwith-Wiedemann syndrome A Mussa, C Molinatto, F Cerrato, O Palumbo, M Carella, G Baldassarre, ... Pediatrics 140 (1), 2017 | 128 | 2017 |
| Thyroid nodules in pediatrics: which ones can be left alone, which ones must be investigated, when and how A Corrias, A Mussa Journal of clinical research in pediatric endocrinology 5 (Suppl 1), 57, 2013 | 110 | 2013 |
| Thyroid function patterns at Hashimoto’s thyroiditis presentation in childhood and adolescence are mainly conditioned by patients’ age M Wasniewska, A Corrias, M Salerno, A Mussa, D Capalbo, MF Messina, ... Hormone research in paediatrics 78 (4), 232-236, 2012 | 100 | 2012 |
| Comparative evaluation of therapy with L-thyroxine versus no treatment in children with idiopathic and mild subclinical hypothyroidism M Wasniewska, A Corrias, T Aversa, M Valenzise, A Mussa, L De Martino, ... Hormone Research in Paediatrics 77 (6), 376-381, 2012 | 98 | 2012 |
| Recommendations of the Scientific Committee of the Italian Beckwith–Wiedemann Syndrome Association on the diagnosis, management and follow-up of the syndrome A Mussa, S Di Candia, S Russo, S Catania, M De Pellegrin, L Di Luzio, ... European journal of medical genetics 59 (1), 52-64, 2016 | 93 | 2016 |
| Predictors of malignancy in children with thyroid nodules A Mussa, M De Andrea, M Motta, A Mormile, N Palestini, A Corrias The Journal of pediatrics 167 (4), 886-892. e1, 2015 | 91 | 2015 |
| Outcomes of children with hashitoxicosis M Wasniewska, A Corrias, M Salerno, F Lombardo, T Aversa, A Mussa, ... Hormone research in paediatrics 77 (1), 36-40, 2012 | 89 | 2012 |
| (Epi) genotype–phenotype correlations in Beckwith–Wiedemann syndrome: a paradigm for genomic medicine A Mussa, S Russo, L Larizza, A Riccio, GB Ferrero Clinical Genetics 89 (4), 403-415, 2016 | 87 | 2016 |
| Peculiarities of Graves' disease in children and adolescents with Down's syndrome F De Luca, A Corrias, M Salerno, M Wasniewska, R Gastaldi, A Cassio, ... European journal of endocrinology 162 (3), 591-595, 2010 | 80 | 2010 |
| A multi-method approach to the molecular diagnosis of overt and borderline 11p15. 5 defects underlying Silver–Russell and Beckwith–Wiedemann syndromes S Russo, L Calzari, A Mussa, E Mainini, M Cassina, S Di Candia, ... Clinical epigenetics 8, 1-15, 2016 | 72 | 2016 |
| Metabolic syndrome in children with Prader–Willi syndrome: the effect of obesity P Brambilla, A Crinò, G Bedogni, L Bosio, M Cappa, A Corrias, ... Nutrition, metabolism and cardiovascular diseases 21 (4), 269-276, 2011 | 72 | 2011 |
Giovanni Battista FerreroAssociate Professor, Department of Clinical nd Biological Sciences, University of TorinoVerified email at unito.it
