| (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 | 145 | 2016 |
| (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 | 89 | 2016 |
| A heritable cause of cleft lip and palate—Van der Woude syndrome caused by a novel IRF6 mutation. Review of the literature and of the differential diagnosis GB Ferrero, G Baldassarre, E Panza, M Valenzise, T Pippucci, A Mussa, ... European journal of pediatrics 169, 223-228, 2010 | 19 | 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 | 69 | 2016 |
| Assessment of central adrenal insufficiency in children and adolescents with Prader–Willi syndrome A Corrias, G Grugni, A Crinò, S Di Candia, P Chiabotto, A Cogliardi, ... Clinical Endocrinology 76 (6), 843-850, 2012 | 51 | 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 | 129 | 2017 |
| Assisted Reproductive Techniques and Risk of Beckwith-Wiedemann Syndrome C Molinatto, F Cerrato, A Mussa, M Carella, G Baldassarre, D Carli, ... | | |
| Bone alterations in children and young adults with renal transplant assessed by phalangeal quantitative ultrasound A Mussa, F Porta, B Gianoglio, M Gaido, MG Nicolosi, F De Terlizzi, ... American journal of kidney diseases 50 (3), 441-449, 2007 | 26 | 2007 |
| Bone impairment in phenylketonuria is characterized by circulating osteoclast precursors and activated T cell increase I Roato, F Porta, A Mussa, L D'Amico, L Fiore, D Garelli, M Spada, ... PLoS One 5 (11), e14167, 2010 | 64 | 2010 |
| Bone quantitative ultrasound in congenital and acquired childhood multiple pituitary failure A Mussa, M Repici, L Fiore, G Tuli, F Porta, P Matarazzo Ultrasound in medicine & biology 36 (5), 726-732, 2010 | 7 | 2010 |
| Breastfeeding effects on newborn screening F Porta, A Mussa, A Ponzone The Journal of pediatrics 156 (6), 1033, 2010 | 4 | 2010 |
| 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 | 163 | 2016 |
| Central adrenal insufficiency in young adults with Prader‐Willi Syndrome G Grugni, L Beccaria, A Corrias, A Crinò, M Cappa, C De Medici, ... Clinical endocrinology 79 (3), 371-378, 2013 | 48 | 2013 |
| Combined treatment with bicalutamide and anastrozole in a young boy with peripheral precocious puberty due to McCune-Albright Syndrome D Tessaris, P Matarazzo, A Mussa, G Tuli, F Verna, L Fiore, R Lala Endocrine journal 59 (2), 111-117, 2012 | 25 | 2012 |
| Comment on “Prenatal diagnosis and prognosis in Noonan syndrome” G Baldassarre, A Mussa, M Silengo, GB Ferrero Prenatal Diagnosis 33 (13), 1318-1320, 2013 | 3 | 2013 |
| 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 |
| Congenital hypothyroidism, cerebellar atrophy, and the incomplete phenotypic expression of PHACES syndrome A Mussa, A Corrias, G Baldassarre, E Biamino, M Silengo Endocrine journal 55 (1), 231-231, 2008 | 4 | 2008 |
| Constitutional bone impairment in Noonan syndrome G Baldassarre, A Mussa, D Carli, C Molinatto, GB Ferrero American Journal of Medical Genetics Part A 173 (3), 692-698, 2017 | 23 | 2017 |
| Determinants of thyrotropin rise in congenital hypothyroidism A Mussa, F Porta, G Baldassarre, A Corrias The Journal of pediatrics 159 (6), 1050, 2011 | 1 | 2011 |
| 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 | 166 | 2010 |
Giovanni Battista FerreroAssociate Professor, Department of Clinical nd Biological Sciences, University of Torino在 unito.it 的电子邮件经过验证
