Laurea Magistrale in Medicina e Chirurgia - sede di Torino

Prodotti della ricerca selezionati

Pubblicazioni in extenso su riviste internazionali

1. Defilippi C, Chiappetta D, Marzari D, Mussa A, Lala R. Image diagnosis in McCune-Albright syndrome. J Pediatr Endocrinol Metab. 2006; 19 (Suppl 2):561-70.
2. Mussa A, Porta F, Gianoglio B, Gaido M, Nicolosi MG, De Terlizzi F, de Sanctis C, Coppo R. Bone alterations in children and young adults with renal transplant assessed by phalangeal quantitative ultrasound. Am J Kidney Dis. 2007; 50:441-9.
3. Mussa A, Corrias A, Baldassarre G, Biamino E, Silengo M. Congenital hypothyroidism, cerebellar atrophy, and the incomplete phenotypic expression of PHACES syndrome. Endocr J. 2008; 55:231.
4. Porta F, Spada M, Lala R, Mussa A. Phalangeal quantitative ultrasound in children with phenylketonuria: a pilot study. Ultrasound Med Biol. 2008; 34:1049-52.
5. Ponzone A, Spada M, Roasio L, Porta F, Mussa A, Ferraris S. Impact of neonatal protein metabolism and nutrition on screening for phenylketonuria. J Pediatr Gastroenterol Nutr. 2008; 46:561-9.
6. Corrias A, Cassio A, Weber G, Mussa A, Wasniewska M, Rapa A, Gastaldi R, Einaudi S, Baronio F, Vigone MC, Messina MF, Bal M, Bona G, de Sanctis C; Study Group for Thyroid Diseases of Italian Society for Pediatric Endocrinology and Diabetology (SIEDP/ISPED). Thyroid nodules and cancer in children and adolescents affected by autoimmune thyroiditis. Arch Pediatr Adolesc Med. 2008; 162:526-31.
7. Mussa A, Baldassarre G, Rosaia De Santis L, Gastaldi R, Corrias A, Silengo MC. Four new cases of PHACES syndrome: variable phenotypic expression and endocrine features. Acta Paediatr. 2008; 97:1729-33.
8. Porta F, Roato I, Mussa A, Repici M, Gorassini E, Spada M, Ferracini R. Increased spontaneous osteoclastogenesis from peripheral blood mononuclear cells in phenylketonuria. J Inherit Metab Dis. 2008; 31 (Suppl 2):S339-42.
9. Wasniewska M, Salerno M, Cassio A, Corrias A, Aversa T, Zirilli G, Capalbo D, Bal M, Mussa A, De Luca F. Prospective evaluation of the natural course of idiopathic subclinical hypothyroidism in childhood and adolescence. Eur J Endocrinol. 2009; 160:417-21.
10. Ferrero GB, Baldassarre G, Panza E, Valenzise M, Pippucci T, Mussa A, Pepe E, Seri M, Silengo MC. 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. Eur J Pediatr. 2009; 18:169:223-8.
11. Wasniewska M, Corrias A, Messina MF, Crisafulli G, Salzano G, Valenzise M, Mussa A, De Luca F. Grave’s disease prevalence in a young population with Turner syndrome. J Endocrinol Invest. 2009; 33:69-70.
12. Ponzone A, Mussa A, Porta F. In response to van Spronsen et al. Phenylalanine tolerance can already reliably be assessed at the age of 2 years in patients with PKU. J Inherit Metab Dis. 2009;32:584.
13. Porta F, Mussa A, Concolino D, Spada M, Ponzone A. Dopamine agonists in 6-pyruvoyl tetrahydropterin synthase deficiency. Neurology. 2009: 73: 633-7.
14. Ferrero GB, Porta F, Biamino E, Mussa A, Garelli1 E , Chiappe F, Veltri A, Cirillo Silengo M, Gennari F. Remittent hyperammonemia in congenital portosystemic shunt. Eur J Pediatr. 2009;169:369-72.
15. Canavese F, Mussa A, Manenti M,  Cortese MG, Ferrero L, Tuli G, Macchieraldo R, Lala R. Sperm Count of Young Men Surgically Treated for Cryptorchidism in the First and Second Year of Life: Fertility Proves Better in Younger Children. Eur J Pediatr Surg. 2009: 19:388-91.
16. Ponzone A, Porta F, Mussa A, Alluto A, Ferraris S, Spada M. Unresponsiveness to tetrahydrobiopterin of phenylalanine hydroxylase deficiency. Metabolism. 2010;59: 645-52.
17. Brambilla P, Crinò A, Bedogni G, Bosio L, Cappa M, Corrias A, Delvecchio M, Di Candia S, Gargantini L, Grechi E, Iughetti L, Mussa A, Ragusa L, Sacco M, Salvatoni A, Chiumello G, Grugni G; on behalf of the Genetic Obesity Study Group of the Italian Society of Pediatric Endocrinology and Diabetology (ISPED): Metabolic syndrome in children with Prader-Willi syndrome: the effect of obesity.  Nutr Metab Cardiovasc Dis. 2010; 21:269-76.
18. De Luca F, Corrias A, Salerno M, Wasniewska M, Gastaldi R, Cassio A, Mussa A, Aversa T, Radetti G, Arrigo T. Peculiarities of Graves' disease in children and adolescents with Down's syndrome. Eur J Endocrinol. 2010; 162: 591-5.
19. Mussa A, Bertorello N, Porta F, Galletto C,Nicolosi MG, Manicone R, Corrias A, Fagioli F. Prospective bone ultrasound patterns during childhood acute lymphoblastic leukemia treatment. Bone 2010: 46:1016-20.
20. Wasniewska M, Corrias A, Arrigo T, Lombardo F, Salerno M, Mussa A, Vigone MC, De Luca F. Frequency of Hashimoto’s Thyroiditis Antecedents in the History of Children and Adolescents with Graves’ Disease. Horm Res Paediatr 2010; 73:473-476.
21. Corrias A, Mussa A, Baronio F, Arrigo T, Salerno M, Segni M, Vigone MC, Gastaldi R, Zirilli G, Tuli G, Beccaria L, Iughetti L, Einaudi S, Weber G, De Luca F, Cassio A. Diagnostic features of thyroid nodules in pediatrics. Arch Pediatr & Adolesc Med. 2010; 164:714-9.
22. Mussa A, Chiesa N,Baldassarre G, Porta F, Cirillo Silengo M,Ferrero GB. The overlap between Sotos and Beckwith-Wiedemann syndromes. J Peds 2010;156(6):1035-6.
23. Porta F, Mussa A, Ponzone A. Breastfeeding effect on newborn screening. J Pediatr 2010;156:1033.
24. Mussa A, Repici M, Fiore L, Tuli G, Porta F, Matarazzo P. Bone quantitative ultrasound in congenital and acquired childhood multiple pituitary failure. Ultrasound Med Biol. 2010; 36:726-32.
25. Mussa A, Bertorello N, Porta F, Galletto C, Nicolosi MG, Manicone R, Corrias A, Fagioli F. Fractures and skeletal complications should be the gold standard for validation of methods for bone appraisal in pediatrics. Bone. 2010;46:1016-20.
26. Corrias A, Mussa A, Wasniewska M, Segni M, Cassio A, Salerno M, Gastaldi R, Vigone MC, Bal M, Matarazzo P, Weber G, De Luca F. Levothyroxine Treatment in Pediatric Benign Thyroid Nodules. Horm Res Paediatr. 2011;75:246-51.
27. Porta F, Mussa A, Zanin A, Greggio NA, Burlina A, Spada M. Impact of metabolic control on bone quality in phenylketonuria and mild hyperphenylalaninemia. J Pediatr Gastroenterol Nutr. 2011;52:345-50.
28. Roato I, Porta F, Mussa A, D’Amico L, Fiore L, Garelli D, Spada M, Ferracini R. Bone Impairment in Phenylketonuria Is Characterized by Circulating Osteoclast Precursors and Activated T Cell Increase. PLoS ONE 2010; 5: e14167.
29. Porta F, Spada M, Garelli D, Mussa A, Ponzone A. Tetrahydrobiopterin and phenylketonuria. J Pediatr. 2011; 158: 864.
30. Porta F, Garelli D, Mussa A. Phenotyping and treatment of phenylketonuria. Lancet. 2011; 377(9764): 465
31. Porta F, Pagliardini S, Pagliardini V, Dotta A, Mussa A, Spada M. Lysosomal enzyme activities in phenylketonuria. Mol Genet Metab. 2011; 102: 508.
32. Mussa A, Ferrero GB, Ceoloni B, Basso E, Chiesa N, De Crescenzo A, Pepe E, Silengo M, de Sanctis L. Neonatal hepatoblastoma in a newborn with severe phenotype of Beckwith-Wiedemann syndrome. Eur J Pediatr. 2011; 170:1407-11.
33. Baldassarre G, Mussa A, Dotta A, Banaudi E, Forzano S, Marinosci A , Rossi C, Tartaglia M, Silengo M, Ferrero GB. Prenatal features of Noonan Syndrome: prevalence and prognostic value. Prenat Diagn 2011; 31:949-54.
34. Mussa A, Peruzzi L, Chiesa N, De Crescenzo A, Russo S, Melis D, Tarani L, Baldassarre G, Larizza L, Riccio A, Silengo M, Ferrero GB. Nephrological findings and genotype-phenotype correlation in Beckwith-Wiedemann syndrome. 2012; 27: 397-406.
35. Mussa A, Porta F, Baldassarre G, Tuli G, de Terlizzi F, Matarazzo P, Einaudi S, Lala R, Corrias A. Phalangeal quantitative ultrasound in 1,719 children and adolescents with bone disorders. Osteoporos Int. 2012; 23: 1987-98.
36. Radetti G, Maselli M, Buzi F, Corrias A, Mussa A, Cambiaso P, Salerno M, Cappa M, Baiocchi M, Gastaldi R, Minerba L, Loche S. The natural history of the normal/mild elevated TSH serum levels in children and adolescents with Hashimoto's thyroiditis and isolated hyperthyrotropinaemia: a three year follow-up. Clin Endocrinol (Oxf). 2012; 76:394-8.
37. Chiesa N, De Crescenzo A, Mishra K, Perone L, Carella M, Palumbo O, Mussa A, Sparago A, Cerrato F, Russo S, Lapi E, Cubellis MV, Kanduri C, Cirillo Silengo M, Riccio A, Ferrero GB. The KCNQ1OT1 Imprinting Control Region and non-coding RNA: new properties derived from the study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome cases. Hum Mol Genet 2012; 21:10-25.
38. Tessaris D, Matarazzo P, Mussa A, Tuli G, Verna F, Fiore L, Lala R. Combined treatment with bicalutamide and anastrozole in a young boy with peripheral precocious puberty due to McCune- Albright Syndrome. Endocr J 2012; 59: 111-7.
39. Mussa A, Porta F, Baldassarre G, Corrias A. Determinants of thyrotropin rise in congenital hypothyroidism. J Pediatr. 2011; 159: 1050.
40. Wasniewska M, Corrias A, Salerno M, Lombardo F, Aversa T, Mussa A, Capalbo D, De Luca F, Valenzise M. The outcomes of children with Hashitoxicosis. Horm Res Paediatr 2012; 77: 36-40.
41. Matarazzo P, Tuli G, Verna F, Tessaris D, Fiore L, Mussa A, Repici M, Lala R. Management of sodium metabolism derangements in children treated for hypothalamic-hypophyseal tumors. J Ped Biochem 2011; 1:289-296.
42. Guanà R, Mussa A, Lala R, Tessaris D, Tessiatore P, Maiullari E, Canavese F. Surgical enucleation of testicular leydigioma in a young child: case report and literature review. J Pediatr Endocr Metab 2011;24:839–842.
43. Corrias A, Grugni G, Crinò A, Di Candia S, Chiabotto P, Cogliardi A, Chiumello G, De Medici C, Spera S, Gargantini L, Iughetti L, Luce A, Mariani B, RagusaL, Salvatoni A, Andrulli S, Mussa A, Beccaria L. Assessment of central adrenal insufficiency in children and adolescents with Prader-Willi syndrome. Clin Endocr (oxf) 2012; 76:843-50.
44. Porta F, Mussa A, Concolino D, Spada M, Ponzone A. Dopamine agonists in dihydropteridine reductase deficiency. Mol Genet Metab 2012; 105:582-4.
45. Mussa A, Camilla R, Monticone S, Porta F, Tessaris D, Verna F, Mulatero P, Einaudi S.Polyuric-polydipsic syndrome in a pediatric case of non-glucocorticoid remediable Familial Hyperaldosteronism. Endocr J 2012; 59:497-502.
46. Tessiatore P, Guanà R, Mussa A, Lonati L, Sberveglieri M, Ferrero L, Canavese F. When to operate on ovarian cysts in children? J Pediatr Endocrinol Metab. 2012 ;25:427-33.
47. Wasniewska M, Corrias A, Aversa T, Valenzise M, Mussa A, De Martino L, Lombardo F, De Luca F, Salerno M.Comparative evaluation of therapy with L-thyroxine versus no treatment in children with idiopathic and mild subclinical hypothyroidism. Horm Res Paediatr 2012; 77:376-81.
48. Garofalo S, Mussa A, Mostert M, Suteu L, Vinardi S, Gamba S, Lonati L, Teruzzi E, Tommasoni N, Bassignana M, Masi G, Marenzi G, Sammartino G, Mortellaro C. Successful medical treatment for ranula in children. Oral Surg Oral Med Oral Pathol Oral Radiol. 2014; 117:e289-97.
49. Wasniewska M, Corrias A, Salerno M, Mussa A, Capalbo D, Messina MF, Aversa T, Bombaci S, De Luca F, Valenzise M. Thyroid Function Patterns at Hashimoto's Thyroiditis Presentation in Childhood and Adolescence Are Mainly Conditioned by Patients' Age. Horm Res Paediatr. 2012; 78:232-6.
50. Corrias A, Mussa A. Thyroid Nodules in Pediatrics: Which Ones Can Be Left Alone, Which Ones Must Be Investigated, When and How. J Clin Res Pediatr Endocrinol. 2013; 5 (Suppl 1):57-69.
51. Grugni G, Beccaria L, Corrias A, Crinò A, Cappa M, De Medici C, Candia SD, Gargantini L, Ragusa L, Salvatoni A, Sartorio A, Spera S, Andrulli S, Chiumello G, Mussa A. Central Adrenal Insufficiency in Young Adults with Prader-Willi Syndrome. Clin Endocrinol (Oxf). 2013; 79:371-8.
52. Porta F, Mussa A, Spada M. Later effects of metabolic control in phenylketonuria. Mol Genet Metab. 2013;79:371-8.
53. Mussa A, Russo S, De Crescenzo A, Chiesa N, Molinatto C, Selicorni A, Richiardi L, Larizza L, Silengo MC, Riccio A, Ferrero GB. Prevalence of Beckwith-Wiedemann syndrome in North West of Italy. Am J Med Genet A. 2013; 161A:2481-6.
54. Feyles F, Peiretti V, Mussa A, Manenti M, Canavese F, Cortese MG, Lala R. Improved sperm count and motility in young men surgically treated for cryptorchidism in the first year of life. Eur J Pediatr Surg. 2014; 24:376-80.
55. Mussa A, Salerno MC, Bona G, Wasniewska M, Segni M, Cassio A, Vigone MC, Gastaldi R, Iughetti L, Santanera A, Capalbo D, Matarazzo P, De Luca F, Weber G, Corrias A. Serum thyrotropin concentration in children with isolated thyroid nodules. J Pediatr. 2013; 163:1465-70.
56. Matarazzo P, Tuli G, Fiore L, Mussa A, Feyles F, Peiretti V, Lala R.Teriparatide (rhPTH) treatment in children with syndromic hypoparathyroidism. J Pediatr Endocrinol Metab. 2013;14:1-7.
57. Feyles F, Mussa A, Peiretti V, Tessaris D, Santanera A, Corrias A, de Sanctis L, Calvo L. Iatrogenic acute pancreatitis due to hypercalcemia in a child with pseudohypoparathyroidism. J Pediatr Endocrinol Metab. 2014; 27:149-52.
58. Aversa T, Valenzise M, Corrias A, Salerno M, Mussa A, Capalbo D, Salzano G, De Luca F, Wasniewska M. Subclinical hyperthyroidism when presenting as initial manifestation of juvenile Hashimoto's thyroiditis: first report on its natural history. J Endocrinol Invest. 2014; 37:303-8.
59. Valenzise M, Aversa T, Corrias A, Mazzanti L, Cappa M, Ubertini G, Scarano E, Mussa A, Messina MF, De Luca F, Wasniewska M. Epidemiology, Presentation and Long-Term Evolution of Graves' Disease in Children, Adolescents and Young Adults with Turner Syndrome. Horm Res Paediatr. 2014; 81:245-50.
60. Mussa A, Matarazzo P, Corrias A. Papillary thyroid cancer and autoimmune polyglandular syndrome. J Pediatr Endocrinol Metab. 2015; 28:793-5.
61. Mussa A, Pagliardini S, Pagliardini V, Molinatto C, Baldassarre G, Corrias A, Silengo MC, Ferrero GB. α-Fetoprotein assay on dried blood spot for hepatoblastoma screening in children with overgrowth-cancer predisposition syndromes. Pediatr Res. 2014; 76:544-8.
62. Mussa A, Baldassarre G, Porta F. Fracture odds and body mass index in children. J Pediatr. 2014; 165:1274.
63. Baldassarre G, Mussa A, Silengo M, Ferrero GB. Comment on "prenatal diagnosis and prognosis in Noonan syndrome". Prenat Diagn. 2013; 33:1318-20.
64. Guanà R, Bucci V, Carbonaro G, Cerrina A, Ferrero L, Teruzzi E, Mussa A, Morra I, Shleef J. Heterotopic pancreas in Meckel's diverticulum in a 7-year-old child with intussusception and recurrent gastrointestinal bleeding: Case report and literature review focusing on diagnostic controversies. Afr J Paediatr Surg. 2014; 11:354-8.
65. Baldassarre G, Mussa A, Banaudi E, Rossi C, Tartaglia M, Silengo M, Ferrero GB. Phenotypic variability associated with the invariant SHOC2 c.4A>G (p.Ser2Gly) missense mutation. Am J Med Genet A. 2014; 164: 3120-5.
66. Aversa T, Valenzise M, Corrias A, Salerno M, De Luca F, Mussa A, Rezzuto M, Lombardo F, Wasniewska M. Underlying Hashimoto's thyroiditis negatively affects the evolution of subclinical hypothyroidism in children irrespectively of other concomitant risk factors. Thyroid. 2015; 25:183-7.
67. Aversa T, Messina MF, Mazzanti L, Salerno M, Mussa A, Faienza MF, Scarano E, De Luca F, Wasniewska M. The association with Turner syndrome significantly affects the course of Hashimoto's thyroiditis in children, irrespective of karyotype. Endocrine. 2015; 50:777-82.
68. Guanà R, Garofano S, Teruzzi E, Vinardi S, Carbonaro G, Cerrina A, Morra I, Montin D, Mussa A, Schleef J. The Complex Surgical Management of the First Case of Severe Combined Immunodeficiency and Multiple Intestinal Atresias Surviving after the Fourth Year of Life. Pediatr Gastroenterol Hepatol Nutr 2014; 17:257-262.
69. Delvecchio M, Salerno M, Vigone MC, Wasniewska M, Popolo PP, Lapolla R, Mussa A, Tronconi GM, D'Acunzo I, Di Mase R, Falcone RM, Corrias A, De Luca F, Weber G, Cavallo L, Faienza MF. Levothyroxine requirement in congenital hypothyroidism: a 12-year longitudinal study. Endocrine. 2015; 50:674-80.
70. Aversa T, Salerno M, Radetti G, Faienza MF, Iughetti L, Corrias A, Predieri B, Mussa A, Mirabelli S, De Luca F, Wasniewska M. Peculiarities of presentation and evolution over time of Hashimoto’s thyroiditis in children and adolescents with Down’s syndrome. Hormones, 2015; 14:410-6.
71. Mussa A, Russo S, De Crescenzo A, Freschi A, Calzari L, Maitz S, Macchiaiolo M, Molinatto C, Baldassarre G, Mariani M, Tarani L, Bedeschi MF, Milani D, Melis D, Bartuli A, Cubellis MV, Selicorni A, Cirillo Silengo M, Larizza L, Riccio A, Ferrero GB. (Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome. Eur J Hum Genet. 2016; 24:183-90.
72. Garofalo S, Mostert M, Morra I, Cortese MG, Guanà R, Mussa A, Canesi M, Carbonaro G, Cerrina A, Ferrero L, Cussa D, Schleef J.Pyogenic Granuloma of the Sigmoid Colon causing Intussusception in an Infant. APSP J Case Rep. 2015; 6:15.
73. Mussa A, Russo S, Larizza L, Riccio A, Ferrero GB. (Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome: a paradigm for genomic medicine. Clin Genet. 2016; 89:403-15.
74. Mussa A, De Andrea M, Motta M, Mormile A, Palestini N, Corrias A. Predictors of Malignancy in Children with Thyroid Nodules. J Pediatr. 2015; 167:886-892.
75. Mussa A, Ferrero GB. Screening Hepatoblastoma in Beckwith-Wiedemann Syndrome: A Complex Issue. J Pediatr Hematol Oncol. 2015; 37:627.
76. Porta F, Mussa A, Baldassarre G, Perduca V, Farina D, Spada M, Ponzone A. Genealogy of breastfeeding. Eur J Pediatr. 2016; 175:105-12.
77. Wasniewska M, Aversa T, Salerno M, Corrias A, Messina MF, Mussa A, Capalbo D, De Luca F, Valenzise M. Five-year prospective evaluation of thyroid function in girls with subclinical mild hypothyroidism of different etiology. Eur J Endocrinol. 2015; 173:801-8.
78. Mussa A, Di Candia S, Russo S, Catania S, De Pellegrin M, Di Luzio L, Ferrari M, Tortora C, Meazzini MC, Brusati R, Milani D, Zampino G, Montirosso R, Riccio A, Selicorni A, Cocchi G, Ferrero GB.. Recommendations of the Scientific Committee of the Italian Beckwith-Wiedemann Syndrome Association on the diagnosis, management, and follow-up of the syndrome. Eur J Med Genet. 2016; 59:52-64.
79. Mussa A, Russo S, De Crescenzo A, Freschi A, Calzari L, Maitz S, Macchiaiolo M, Molinatto C, Baldassarre G, Mariani M, Tarani L, Bedeschi MF, Milani D, Melis D, Bartuli A, Cubellis MV, Selicorni A, Silengo MC, Larizza L, Riccio A, Ferrero GB. Fetal growth patterns in Beckwith-Wiedemann syndrome. Clin Genet. 2016 ;90:21-7.
80. Russo S, Calzari L, Mussa A, Mainini E, Cassina M, Di Candia S, Clementi M, Guzzetti S, Tabano S, Miozzo M, Sirchia S, Finelli P, Prontera P, Maitz S, Sorge G, Calcagno A, Maghnie M, Divizia MT, Melis D, Manfredini E, Ferrero GB, Pecile V, Larizza L. A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes. Clin Epigenetics. 2016; 8:23.
81. Mussa A, Molinatto C, Baldassarre G, Riberi E, Russo S, Larizza L, Riccio A, Ferrero GB. Cancer Risk in Beckwith-Wiedemann Syndrome: A Systematic Review and Meta-Analysis Outlining a Novel (Epi)Genotype Specific Histotype Targeted Screening Protocol. J Pediatr. 2016; 176:142-149.
82. van Dorp W, Mulder RL, Kremer LC, Hudson MM, van den Heuvel-Eibrink MM, van den Berg MH, Levine JM, van Dulmen-den Broeder E, di Iorgi N, Albanese A, Armenian SH, Bhatia S, Constine LS, Corrias A, Deans R, Dirksen U, Gracia CR, Hjorth L, Kroon L, Lambalk CB, Landier W, Levitt G, Leiper A, Meacham L, Mussa A, Neggers SJ, Oeffinger KC, Revelli A, van Santen HM, Skinner R, Toogood A, Wallace WH, Haupt R. Recommendations for Premature Ovarian Insufficiency Surveillance for Female Survivors of Childhood, Adolescent, and Young Adult Cancer: A Report From the International Late Effects of Childhood Cancer Guideline Harmonization Group in Collaboration With the PanCareSurFup Consortium. J Clin Oncol. 2016; 34:3440-50.
83. Lemini R, Guanà R, Tommasoni N, Mussa A, Di Rosa G, Schleef J. Predictivity of Clinical Findings and Doppler Ultrasound in Pediatric Acute Scrotum. Urol J. 2016; 13:2779-83.
84. Baldassarre G, Mussa A, Carli D, Molinatto C, Ferrero GB. Constitutional bone impairment in Noonan syndrome. Am J Med Genet A. 2017;173:692-698.
85. Mussa A, Ferrero GB. Serum alpha-fetoprotein screening for hepatoblastoma in Beckwith-Wiedemann syndrome. Am J Med Genet A. 2017; 173:585-587.
86. Manzoni P, García Sánchez R, Meyer M, Stolfi I, Pugni L, Messner H, Cattani S, Betta PM, Memo L, Decembrino L, Bollani L, Rinaldi M, Fioretti M, Quercia M, Maule M, Tavella E, Mussa A, Tzialla C, Laforgia N, Mosca F, Magaldi R, Mostert M, Farina D; Italian Task Force for the Study, and Prevention of Neonatal Fungal Infections and the Italian Society of Neonatology. Exposure to Gastric Acid Inhibitors Increases the Risk of Infection in Preterm Very Low Birth Weight Infants but Concomitant Administration of Lactoferrin Counteracts This Effect. J Pediatr. 2018; 193:62-67.
87. Mussa A, Molinatto C, Cerrato F, Palumbo O, Carella M, Baldassarre G, Carli D, Peris C, Riccio A, Ferrero GB. Assisted Reproductive Techniques and Risk of Beckwith-Wiedemann Syndrome. Pediatrics. 2017;140. pii: e20164311. doi: 10.1542/peds.2016-4311.
88. Kalish JM, Biesecker LG, Brioude F, Deardorff MA, Di Cesare-Merlone A, Druley T, Ferrero GB, Lapunzina P, Larizza L, Maas S, Macchiaiolo M, Maher ER, Maitz S, Martinez-Agosto JA, Mussa A, Robinson P, Russo S, Selicorni A, Hennekam RC. Nomenclature and definition in asymmetric regional body overgrowth. Am J Med Genet A. 2017. doi: 10.1002/ajmg.a.38266.
89. Brioude F, Kalish JM, Mussa A, Foster AC, Bliek J, Ferrero GB, Boonen SE, Cole T, Baker R, Bertoletti M, Cocchi G, Coze C, De Pellegrin M, Hussain K, Ibrahim A, Kilby MD, Krajewska-Walasek M, Kratz CP, Ladusans EJ, Lapunzina P, Le Bouc Y, Maas SM, Macdonald F, Õunap K, Peruzzi L, Rossignol S, Russo S, Shipster C, Skórka A, Tatton-Brown K, Tenorio J, Tortora C, Grønskov K, Netchine I, Hennekam RC, Prawitt D, Tümer Z, Eggermann T, Mackay DJG, Riccio A, Maher ER. Expert consensus document: Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: an international consensus statement. Nat Rev Endocrinol. 2018; 14:229-249.
90. Montin D, Licciardi F, Giorgio E, Ciolfi A, Pizzi S, Mussa A, Meazza R, Tartaglia M, Brusco A, Pende D, Ferrero GB. Functional evaluation of natural killer cell cytotoxic activity in NFKB2-mutated patients. Immunol Lett. 2018; 194:40-3.
91. Carbonell-Estrany X, Dall'Agnola A, Fullarton JR, Rodgers-Gray BS, Girardi E, Mussa A, Paniagua N, Pieretto M, Rodríguez-Fernandez R, Manzoni P. Interaction between healthcare professionals and parents is a key determinant of parental distress during childhood hospitalisation for respiratory syncytial virus infection (European RSV Outcomes Study [EROS]). Acta Paediatr. 2018; 107:854-860.
92. Brioude F, Hennekam R, Bliek J, Coze C, Eggermann T, Ferrero GB, Kratz C, Bouc YL, Maas SM, Mackay DJG, Maher ER, Mussa A, Netchine I. Revisiting Wilms tumour surveillance in Beckwith-Wiedemann syndrome with IC2 methylation loss, reply. Eur J Hum Genet. 2018; 26:471-472.

 

Capitoli di libri e libri

 

• Corrias A, Mussa A, Grossi A, Cappa M. Thyroid Nodules and Carcinoma. In: Bona G, De Luca F, Monzani A (Eds.) Thyroid Diseases in Childhood. Recent Advances from Basic Science to Clinical Practice. Springer. 2015, 1st edition. (ISBN 978-3-319-19213-0)
• Mussa A, Porta F, Hoffmann GF, Sarafoglou K. Emergency assessment and management of suspected inborn errors of metabolism and endocrine disorders. In Pediatric Endocrinology and Inborn Errors of metabolism, 2^nd edition. Sarafoglou K, Hoffmann GF, Roth KS eds. McGraw-Hill Education, New York: 2017 (ISBN 0071773142)
• Mussa A, Ferrero GB. Sindrome di Beckwith-Wiedemann. In: Le sindromi polimarformative: una guida per il pediatra. Selicorni A, Zampino G, Memo L, Scarano G eds. Pacini Editore Medicina 2017, p115-120 (ISBN 978-88-6995-201-2)

 

 

Insegnamenti

• Modulo Neonatologia (MED3020B)
  Corso di Laurea in Terapia della Neuro e Psicomotricità dell'Età Evolutiva
• PEDIATRIA GENERALE (MED3431A)
  Corso di Laurea in Infermieristica Pediatrica
• PROBLEMI DI SALUTE IN PEDIATRIA I (MED3431)
  Corso di Laurea in Infermieristica Pediatrica
• Patologia dell'infanzia (MED2707)
  Corso di Laurea Magistrale in Odontoiatria e Protesi Dentaria
• Pediatria (MED3116B)
  Corso di laurea in Tecniche Audiometriche
• Pediatria (MED2707C)
  Corso di Laurea Magistrale in Odontoiatria e Protesi Dentaria
• Pediatria (canale C) (MED0203)
  Laurea Magistrale in Medicina e Chirurgia - sede di Torino
• Pediatria (canale D) (MED0203)
  Laurea Magistrale in Medicina e Chirurgia - sede di Torino
• SCIENZE CLINICHE, PSICOPEDAGOGICHE DELL'ETA' EVOLUTIVA (MED3116)
  Corso di laurea in Tecniche Audiometriche
• SCIENZE CLINICHE, PSICOPEDAGOGICHE DELL'ETA' EVOLUTIVA (MED3180)
  Corso di laurea in Tecniche Audioprotesiche
• SCIENZE PEDIATRICHE E MEDICO CHIRURGICHE (270/04) (MED3020)
  Corso di Laurea in Terapia della Neuro e Psicomotricità dell'Età Evolutiva
• Scienze Pediatriche (MED3180B)
  Corso di laurea in Tecniche Audioprotesiche

Temi di ricerca

Genetica Clinica Pediatrica

SC Pediatria specialistica U
SC Specialistic Pediatrics U

Attività in agenda

Consulta la mia agenda

Organi

• AVA 3 - PO_PA
• Commissione Bilancio 2021-2024
• Consiglio di Dipartimento DSSPP
• elenco PO_PA_RIC_TR

Ricevimento studenti

Ricevimento da concordarsi previo accordo telefonico o via e-mail (alessandro.mussa@unito.it) preferibilmente su Webex Meetings (https://unito.webex.com/meet/alessandro.mussa).