PUBBLICAZIONI

In questa sezione sono riportate le pubblicazioni derivanti dai dati del Registro e dagli studi multicentrici generati dall’attività del Registro.

Newborn screening for congenital hypothyroidism: the benefit of using differential TSH cutoffs in a two-screen program. Caiulo S, Corbetta C, Di Frenna M, Medda E, De Angelis S, Rotondi D, Vincenzi G, de Filippis T, Patricelli MG, Persani L, Barera G, Weber G, Olivieri A, Vigone MC. J Clin Endocrinol Metab. 2021;106(1):e338-e349  https://pubmed.ncbi.nlm.nih.gov/33124651/

Neonatal Screening for Congenital Hypothyroidism: What Can We Learn From Discordant Twins? Medda E, Vigone MC, Cassio A, Calaciura F, Costa P, Weber G, de Filippis T, Gelmini G, Di Frenna M, Caiulo S, Ortolano R, Rotondi, Bartolucci M, Gelsomino R, De Angelis S, Gabbianelli M, Persani L, and Olivieri A. J Clin Endocrinol Metab 2019; 104(12):5765-5779. https://pubmed.ncbi.nlm.nih.gov/31287502/

Are lower TSH cutoffs in neonatal screening for congenital hypothyroidism warranted? Lain S, Trumpff C, Grosse SD, Olivieri A, Van Vliet G. Eur J Endocrinol 2017; 177(5):D1-D12. https://pubmed.ncbi.nlm.nih.gov/28694389/

MULTIPLE FACTORS INFLUENCING THE INCIDENCE OF CONGENITAL HYPOTHYROIDISM DETECTED BY NEONATAL SCREENING. Olivieri A, Fazzini C, Medda E and Italian Study Group for Congenital Hypothyroidism. Horm Res Paediatr 2015; 83(2):86-93. https://pubmed.ncbi.nlm.nih.gov/25572470/

INCIDENCE OF CONGENITAL HYPOTHYROIDISM IN THE AUTONOMOUS PROVINCE OF BOLZANO: BENEFIT OF INCREASED IODINE INTAKE. Olivieri A, Rdetti G, Medda E and Italian Study Group for Congenital Hypothyroidism.  J Endocrinol Invest 2015; 38(2):185-7. https://pubmed.ncbi.nlm.nih.gov/25403430/

CONGENITAL HYPOTHYROIDISM DUE TO DEFECTS OF THYROID DEVELOPMENT AND MILD INCREASE OF TSH AT SCREENING: DATA FROM THE ITALIAN NATIONAL REGISTRY OF INFANTS WITH CONGENITAL HYPOTHYROIDISM. Olivieri A, Corbetta C, Weber G, Vigone M C, Fazzini C, Medda and Italian Study Group for Congenital Hypothyroidism. J Clin Endocrinol Metab 2013; 98(4):1403-1408. https://pubmed.ncbi.nlm.nih.gov/23443814/

THE ITALIAN SCREENING PROGRAM FOR PRIMARY CONGENITAL HYPOTHYROIDISM: ACTIONS TO IMPROVE SCREENING, DIAGNOSIS, FOLLOW UP, AND SURVEILLANCE. A. Cassio, C. Corbetta, I. Antonozzi, F. Calaciura, U. Caruso, G. Cesaretti, R. Gastaldi, E.Medda, F. Mosca, E. Pasquini, MC. Salerno, V. Stoppioni, M. Tonacchera, G. Weber and A. Olivieri. J Endocrinol Invest 2013; 36: 195-203. https://pubmed.ncbi.nlm.nih.gov/23404215/

EPIDEMIOLOGY OF CONGENITAL HYPOTHYROIDISM: WHAT CAN BE DEDUCED FROM THE ITALIAN REGISTRY OF INFANTS WITH CONGENITAL HYPOTHYROIDISM. Olivieri A, Italian Study Group for Congenital Hypothyroidism. J Matern Fetal Neonatal Med 2012; 5(Suppl 5):7-9. https://pubmed.ncbi.nlm.nih.gov/23025761/

THE ITALIAN NATIONAL REGISTER OF INFANTS WITH CONGENITAL HYPOTHYROIDISM: TWENTY YEARS OF SURVEILLANCE AND STUDY OF CONGENITAL HYPOTHYROIDISM. Olivieri A and The Study Group for Congenital Hypothyroidism. Italian Journal of Pediatrics 2009; 35:2. https://pubmed.ncbi.nlm.nih.gov/19490661/

HIGH RISK OF CONGENITAL HYPOTHYROIDISM IN MULTIPLE PREGNANCIES. A. Olivieri, E. Medda, S. De Angelis et al. J Clin Endocrinol & Metab 2007; 92 (8):3141-3147. https://pubmed.ncbi.nlm.nih.gov/17488789/

MISSENSE MUTATION IN THE TRANSCRIPTION FACTOR NKX2-5: A NOVEL MOLECULAR EVENT IN THE PATHOGENESIS OF THYROID DYSGENESIS'. M. Dentice, V. Cordeddu, A.M. Rosica et al. J. Clin. Endocrinol. & Metab 2006; 91(4):1428-1433. https://pubmed.ncbi.nlm.nih.gov/16418214/

RISK FACTORS FOR CONGENITAL HYPOTHYROIDISM: RESULTS OF A POPULATION CASE-CONTROL STUDY (1997-2003). E. Medda, A. Olivieri, M.A. Stazi et al. Eur. J. Endocrinol 2005; 153:765-773. https://pubmed.ncbi.nlm.nih.gov/16322381/

A POPULATION- BASED STUDY ON THE FREQUENCY OF ADDITIONAL CONGENITAL MALFORMATION IN INFANTS WITH CONGENITAL HYPOTHYROIDISM. A. Olivieri, M.A. Stazi, P. Mastroiacovo et al. J. Clin. Endocrinol. Metab 2002; 87: 557-562. https://pubmed.ncbi.nlm.nih.gov/11836285/

UNA PAGINA WEB PER IL REGISTRO NAZIONALE DEGLI IPOTIROIDEI CONGENITI. Sorcini M., Olivieri A., Grandolfo M. et al. Notiziario dell'Istituto Superiore di Sanità. 2000; 13 (7). ALLEGATO Notiziario dell'Istituto Superiore di Sanità. 1feb62ad-43dd-1011-4e0c-6839af083b11 (iss.it)

FORME CONGENITE DI IPOTIROIDISMO: STUDIO DEI FATTORI DI RISCHIO E INTERVENTI DI PREVENZIONE. A. Olivieri, C. Fazzini, M.E. Grandolfo et al. Eds: G. Benagiano, S. Carta, R. Guerra. Ann. Ist. Super. Sanità. 1999; 35 (2): 273-282. https://pubmed.ncbi.nlm.nih.gov/10645661/

IPOTIROIDISMO CONGENITO TRANSITORIO IN AREE IODOCARENTI. A. Olivieri, C. Fazzini, M.E. Grandolfo et al. Eds: A. Pinchera, M. Sorcini, L. Chiovato. Ann. Ist. Super. Sanità. 1998; 34 (3): 331-336.  https://pubmed.ncbi.nlm.nih.gov/10052170/

LO SCREENING NEONATALE DELL' IPOTIROIDISMO CONGENITO IN ITALIA. IL REGISTRO NAZIONALE. M. Sorcini, C. Fazzini, A. Olivieri et al. Eds.: S. Carta, L. Chiovato, G. Giovannelli e A. Pinchera. Ann. Ist. Super. Sanità. 1994; 30 (3): 275. https://pubmed.ncbi.nlm.nih.gov/7879993/

VALUTAZIONE DEI FATTORI DI RISCHIO DELL'IPOTIROIDISMO CONGENITO: PROSPETTIVE DI UNO STUDIO CASO CONTROLLO. M.E. Grandolfo, L. Sagliocca, M.A. Stazi et al. Eds.: S. Carta, L. Chiovato, G. Giovannelli e A. Pinchera. Ann. Ist. Super. Sanità. 1994; 30 (3): 295. https://pubmed.ncbi.nlm.nih.gov/7879995/

THE NATIONAL REGISTER OF INFANTS WITH CONGENITAL HYPOTHYROIDISM DETECTED BY NEONATAL SCREENING IN ITALY. M. Sorcini, P. Balestrazzi, M.E. Grandolfo et al. J. Endocrinol. Invest 1993; 16: 573-77. https://pubmed.ncbi.nlm.nih.gov/8258644/

IL REGISTRO NAZIONALE DEGLI IPOTIROIDEI CONGENITI. M. Sorcini Carta, C. Fazzini, A. Olivieri, et al. Ann. Ist. Super. Sanità. 1992; 28 (4): 533-46. https://pubmed.ncbi.nlm.nih.gov/1303048/

IPOTIROIDISMO CONGENITO: ORGANIZZAZIONE E COORDINAMENTO DELLO SCREENING NEONATALE IN ITALIA. S. Carta, M.E. Grandolfo, L. Moschini, et al. Ann. Ist. Super. Sanità. 1991; 27 (2): 311-18. https://pubmed.ncbi.nlm.nih.gov/1755585/