Pubblicazioni degli ultimi 5 anni:

• Impact of molecular genetics on congenital adrenal hyperplasia management.
  Balsamo A, Baldazzi L, Menabò S, Cicognani A. Sex Dev. 2010 Sep;4(4-5):233-48. Epub 2010 Jul 15. Review. ERRATUM Sex Dev (DOI:10 1159/000342192) Published online: August 24,2012.

• A sequence variation in 3’UTR of CYP21A2 gene correlates with a mild form of congenital adrenal hyperplasia.
  Menabò S, Balsamo A, Baldazzi L, Barbaro M, Nicoletti A, Conti V, Pirazzoli P, Wedell A, Cicognani A. J Endocrinol Invest 2012 Mar; 35(3):298-305.
  

• Increased large artery intima media thickness in adolescents with either classical or non-classical congenital  adrenal hyperplasia.
  Wasniewska M, Balsamo A, Valenzise M, Manganaro A, Faggioli G, Bombaci S, Conti V, Ferri M, Aversa T, Cicognani A, De Luca F.  J Endocrinol Invest. 2013 Jan; 36(1):12-5. doi: 10.3275/8194. Epub 2011 Dec 21. PubMed PMID: 22189488.

• High prevalence of precocious puberty and obesity in childhood narcolepsy with cataplexy.
  Poli F, Pizza F, Mignot E, Ferri R, Pagotto U, Taheri S, Finotti E, Bernardi F, Pirazzoli P, Cicognani A, Balsamo A, Nobili L, Bruni O, Plazzi G. Sleep. 2013 Feb 1;36(2):175-81. doi: 10.5665/sleep.2366. PubMed PMID: 23372264; PubMed Central PMCID: PMC3543059.

• Comparison between Liquid and Tablet Formulations of Levothyroxine in the Initial Treatment of Congenital Hypothyroidism.
  Cassio A, Monti S, Rizzello A, Bettocchi I, Baronio F, D’Addabbo G, Bal MO, Balsamo A. J Pediatr. 2013 Jun;162(6):1264-9, 1269.e1-2. doi: 10.1016/j.jpeds.2012.11.070. Epub 2013 Jan 11. PubMed PMID: 23312689.

• Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations.
  Menabò S, Polat S, Baldazzi L, Kulle AE, Holterhus PM, Grötzinger J, Fanelli F, Balsamo A*, Riepe FG. Corresponding Author & Shared seniorship with FG Riepe. Eur J Hum Genet. 2013 Sep 11. doi: 10.1038/ejhg.2013.197. [Epub ahead of print] PubMed PMID: 24022297.

• Severe obesity and cardiometabolic risk in children: comparison from two international classification systems.     
  Giuliana Valerio, Claudio Maffeis, Antonio Balsamo, Emanuele Miraglia Del Giudice, Claudia Brufani, Graziano Grugni, Maria Rosaria Licenziati, Paolo Brambilla, Melania Manco, Nicola Corciulo, Massimiliano Don, Paola Iaccarino Idelson, Elisabetta Modestini, Giuseppe Morino,  Beatrice Moro, Rita Tanas, on the behalf of the Childhood Obesity Group of the Italian Society of Pediatric Endocrinology and Diabetology.
  PLoS One. 2013 Dec 27;8(12):e83793. doi: 10.1371/journal.pone.0083793. eCollection 2013. PubMed PMID: 24386280; PubMed Central PMCID: PMC3873982.

• Novel associations in disorders of sex development: findings from the I-DSD Registry.
  Cox K, Bryce J, Jiang J, Rodie M, Sinnott R, Alkhawari M, Arlt W, Audi L, Balsamo A, Bertelloni S, Cools M, Darendeliler F, Drop S, Ellaithi M, Guran T, Hiort O, Holterhus PM, Hughes I, Krone N, Lisa L, Morel Y, Soder O, Wieacker P, Ahmed SF. J Clin Endocrinol Metab. 2014 Feb;99(2):E348-55. doi: 10.1210/jc.2013-2918. Epub 2013 Dec 3. PubMed PMID: 24302751.

• Comment on ‘‘Complete Androgen Insensitivity Syndrome:Optimizing Diagnosis and Management’’
  Antonio Balsamo, Federico Baronio, Marta Berra, Silvano Bertelloni, Franco D’Alberton, GiacintoMarrocco, and Santiago Vallasciani. Case Reports in Obstetrics and Gynecology, Hindawi Publishing Corporation, Volume 2014, Article ID 285715, 3 pages; http://dx.doi.org/10.1155/2014/285715

• Rare Diseases Research and Practice.
  Polizzi A, Balsamo A, Bal MO, Taruscio D. In Olaf Hiort and Faisal Ahmed MD: Understanding Differences and Disorders of Sex Development;      Corresponding Author together with Taruscio D. Endocr Dev. Basel, Karger 2014, Vol. 27, pp234-256, (DOI:1159/000363670)

• Changes Over Time In Sex Assignment For Disorders Of Sex Development.
  Zofia Kolesinska, S Faisal Ahmed, Marek Niedziela, Jillian Bryce, Marta Molinska-Glura, Martina Rodie, Jipu Jiang, Richard O Sinnott, Ieuan A Hughes, Feyza Darendeliler, Olaf Hiort, Yvonne van der Zwan, Martine Cools, Tulay Guran, Paul-Martin Holterhus, Silvano Bertelloni, Lidka Lisa, Wiebke Arlt, Nils Krone, Mona Ellaithi,  Antonio Balsamo, Inas Mazen, Anna Nordenstrom,  Katherine Lachlan, Mona Alkhawari MD, Pierre Chatelain, Naomi Weintrob. PEDIATRICS Volume 134, Number 3, September 2014; Pediatrics. 2014 Aug 4. pii: peds.2014-1088. [Epub ahead of print]; PMID:25092939; [PubMed – as supplied by publisher]

•  Quality of Life and Psychological Adjustment of Women Living with 46,XY Differences of Sex Development.
  D’Alberton F, Assante MT, Foresti M, Balsamo A, Bertelloni S, Dati E, Nardi L, Bacchi ML, Mazzanti L.
  J Sex Med. 2015 Jun;12(6):1440-9. doi: 10.1111/jsm.12884. Epub 2015 Apr 20. PubMed PMID: 25893774.

• Improving the diagnosis of 11β-hydroxylase deficiency using home-made MLPA probes: identification of a novel chimeric CYP11B2/CYP11B1 gene in a Sicilian patient. Menabò S, Boccassini S, Gambineri A, Balsamo A, Pasquali R, Prontera O,  Mazzanti L, Baldazzi L.
  J Endocrinol Invest. 2016 Mar;39(3):291-5. doi: 10.1007/s40618-015-0362-z. Epub 2015 Aug 18. PMID:26280318

• Triglycerides-to-HDL cholesterol ratio as screening tool for impaired glucose tolerance in obese children and adolescents.
  Manco M, Grugni G, Di Pietro M, Balsamo A, Di Candia S, Morino GS, Franzese A, Di Bonito P, Maffeis C, Valerio G. Acta Diabetol. 2016 Jun;53(3):493-8. doi: 10.1007/s00592-015-0824-y. Epub 2015 Dec 21. PubMed PMID: 26687197.

• Growing Up With Type 1 Narcolepsy: Its Anthropometric and Endocrine Features.
  Ponziani V, Gennari M, Pizza F, Balsamo A, Bernardi F, Plazzi G. J Clin Sleep Med. 2016 Sep 29. pii: jc-00255-16. PubMed PMID: 27707443. IF 3.429

• Two Moroccan Sisters Presenting with a Severe Salt-Wasting Form of Congenital Adrenal Hyperplasia but Normal Female Genitalia.
  Scaramuzzo RT, Menabò S, Baldazzi L, Moscuzza F, Saba A, Balsamo A, Boldrini A, Ghirri P. Sex Dev. 2017;11(2):82-85. doi: 10.1159/000456023. Epub 2017 Feb 11. PubMed PMID:28190008. IF 1.972

• Childhood obesity classification systems and cardiometabolic risk factors: a comparison of the Italian, World Health Organization and International Obesity Task Force references.
  Valerio G, Balsamo A, Baroni MG, Brufani C, Forziato C, Grugni G, Licenziati,MR, Maffeis C, Miraglia Del Giudice E, Morandi A, Pacifico L, Sartorio A, Manco M; on the behalf of the Childhood Obesity Group of the Italian Society of Pediatric Endocrinology and Diabetology. Ital J Pediatr. 2017 Feb 4;43(1):19. doi: 10.1186/s13052-017-0338-z. PubMed PMID: 28257654. IF1.668

• A genetic epidemiology study of Congenital Adrenal Hyperplasia in Italy.
  Gialluisi A, Menabò S, Baldazzi L, Casula L, Meloni A, Farci MC, Mariotti S, Balestrino L, Ortolano R, Murru S, Carcassi C, Loche S, Balsamo A, Romeo G. Clin Genet. 2017 Jun 23. doi: 10.1111/cge.13078. [Epub ahead of print] PubMed PMID: 28644547. IF 3.326

• Global Application of  the Assessment of Communication Skills of Paediatric Endocrinology Fellows in the Management of Differences in Sex Development Using the ESPE E-Learning.Org Portal.
  Kranenburg LJC, Reerds STH, Cools M, Alderson J, Muscarella M, Magrite E, Kuiper M, Abdelgaffar S, Balsamo A, Brauner R, Chanoine JP, Deeb A, Fechner P, German A, Holterhus PM, Juul A, Mendonca BB, Neville K, Nordenstrom A, Oostdijk W, Rey RA, Rutter MM, Shah N, Luo X, Grijpink K, Drop SLS. Horm Res Paediatr. 2017 Jul 7. doi: 10.1159/000475992. [Epub ahead of print] PubMed PMID: 28689203. IF 1.844

• Bone Mineral Density in Women Living with Complete Androgen Insensitivity Syndrome and Intact Testes or Removed Gonads.
  Bertelloni S, Meriggiola MC, Dati E, Balsamo A, Baroncelli GI. Sex Dev. 2017 Jul 18. doi: 10.1159/000477599. [Epub ahead of print] PubMed PMID: 28715798. IF 1.972

• Identification of a Novel Mutation (p.G328W) in the NR5A1 Gene in a Boy with 46, XY DSD: Case Report of Clinical, Endocrine and Genetic Features
  Ortolano R, Baldazzi L, Menabò S, Balsamo A, Cassio A, Antona V, Cimador M, Corsello G and Giuffrè M. Glob J Endocrinol Metab.2017,  1(1). GJEM.000503. 2017.

• The rehabilitation of children and adolescents with severe or medically complicated obesity: an ISPED expert opinion document. Grugni Graziano, Licenziati Maria Rosaria, Valerio Giuliana, Crinò Antonino, Maffeis Claudio, Tanas Rita, Morino Giuseppe Stefano, Ambruzzi Amalia, Balsamo Antonio, Bellone Simonetta, Bernasconi Sergio, Bianchi Vanessa, Bobbio Adriana, Bruzzi Patrizia, Buongiovanni Carmen, Calcagno Annalisa, Calcaterra Valeria, Canali Teresa, Cerutti Franco, Corciulo Nicola, Cotugno Fortunato, Cuccarolo Giuliano, D’Amico Osvaldo, Di Bonito Procolo, Di Candia Stefania, Di Pietrantonio Violetta, Di Pietro Mario, Filannino Grazia, Fintini Danilo, Forziato Claudia, Franceschi Roberto, Franzese Adriana, Galeazzi Daniela, Gargantini Luigi, Franca Giusti Lia, Gualtieri Antonella, Iafusco Dario, Laura Iezzi Maria, Iughetti Lorenzo, Lera Riccardo, Limauro Raffaele, Lombardi Francesca, Lucchesi Sonia, Macchiaroli Annamaria, Maltoni Giulio, Manco Melania, Miraglia Del Giudice Emanuele, Modestini Elisabetta, Morandi Anita, Mozzillo Enza, Nanni Laura, Nicolosi Alessandra, Pellegrin Maria Chiara, Peruzzi Sonia, Peverelli Paola, Purromuto Salvatore, Ragusa Letizia, Rosato Teresa, Salvo Caterina, Sartori Chiara, Sticco Maura, Elisabeth Street Maria, Trifirò Giuliana, Vianelli Patrizia, Yiannakou Pietro. Eating and Weight Disorders, 2017, 22: 3-12. https://doi.org/10.1007/s40519-016-0305-5

• Characteristics of a nationwide cohort of patients presenting with isolated hypogonado-tropic hypogonadism (IHH)
  Bonomi M^1,2, Vezzoli V², Krausz C³, Guizzardi F², Vezzani S^4,5,6, Simoni M^4,5,6, Bassi I², Duminuco P², Di Iorgi N⁷, Giavoli C^8,9, Pizzocaro A¹⁰, Russo G¹¹, Moro M², Fatti L², Ferlin A¹², Mazzanti L¹³, Zatelli MC¹⁴, Cannavò S¹⁵, Isidori AM¹⁶, Pincelli AI¹⁷, Prodam F¹⁸, Mancini A¹⁹, Limone P²⁰, Tanda ML²¹, Gaudino R²², Salerno M²³, Francesca P²⁴, Maghnie M⁹, Maggi M³, Persani L^8,2; Italian Network on Central Hypogonadism. Collaborators (116): Aimaretti G, Altobelli M, Ambrosio MR, Andrioli M, Angeletti G, Arecco F, Arnaldi G, Arosio M, Balsamo A, Baldassarri M, Bartalena L, Bazzoni N, Beccaria L, Beck-Peccoz P, Bellastella G, Bellizzi M, Benedicenti F, Bernasconi S, Bizzarri C, Bona G, Bonadonna S, Borretta G, Boschetti M, Brunani A, Brunelli V, Buzi F, Cacciatore C, Cangiano B, Cappa M, Casalone R, Cassio A, Cavarzere P, Cherubini V, Ciampani T, Cicognani D, Cignarelli A, Cisternino M, Colombo P, Corbetta S, Corciulo N, Corona G, Cozzi R, Crivellaro C, Dalle Mule I, Danesi L, D’Elia AV, Degli Uberti E, De Leo S, Della Valle E, De Marchi M, Di Iorgi N, Di Mambro A, Fabbri A, Foresta C, Forti G, Franceschi AR, Garolla A, Ghezzi M, Giacomozzi C, Giusti M, Grosso E, Guabello G, Guarneri MP, Grugni G, Isidori AM, Lanfranco F, Lania A, Lanzi R, Larizza L, Lenzi A, Loche S, Loli P, Lombardi V, Maggio MC, Mandrile G, Manieri C, Mantovani G, Marelli S, Marzullo M, Mencarelli MA, Migone N, Motta G, Neri G, Padova G, Parenti G, Pasquino B, Pia A, Piantanida E, Pignatti E, Pilotta A, Pivetta B, Pollazzon M, Pontecorvi A, Porcelli P, Pozzan GB, Pozzobon G, Radetti G, Razzore P, Rocchetti L, Roncoroni R, Rossi G, Sala E, Salvatoni A, Salvini F, Secco A, Segni M, Selice R, Sgaramella P, Sileo F, Sinisi AA, Sirchia F, Spada A, Tresoldi A, Vigneri R, Weber G, Zucchini S. Eur J Endocrinol. 2018 Jan;178(1):23-32. https://doi.org/10.1530/EJE-17-0065 . PMID: 28882981 https://www.ncbi.nlm.nih.gov/pubmed/28882981

• A genetic epidemiology study of Congenital Adrenal Hyperplasia in Italy. Gialluisi A, Menabò S, Baldazzi L, Casula L, Meloni A, Farci MC, Mariotti S, Balestrino L, Ortolano R, Murru S, Carcassi C, Loche S, Balsamo A, Romeo G. Clin Genet. 2018 Feb;93(2):223 https://www.ncbi.nlm.nih.gov/pubmed/28644547
  PMID: 28644547

• Normative Basal Values of Hormones and Proteins of Gonadal and Adrenal Functions from Birth to Adulthood.
  Fanelli F, Baronio F, Ortolano R, Mezzullo M, Cassio A, Pagotto U, Balsamo A.  Sex Dev. 2018 Feb 14;12(1-3).. https://www.ncbi.nlm.nih.gov/pubmed/29439271
  PMID: 29439271

• Mutational and functional studies on NR5A1 gene in 46,XY DSD: identification of six novel loss of function mutations. Rocca MS, Ortolano R, Menabò S, Baronio F, Cassio A, Russo G, Balsamo A, Ferlin A, Baldazzi L. Fertil Steril. 2018 Jun;109(6):1105-1113. doi: 10.1016/j.fertnstert.2018.02.123. PMID: 29935645. https://www.ncbi.nlm.nih.gov/pubmed/29935645

• Involving individuals with disorders of sex development and their parents in exploring new models of shared learning: Proceedings from a DSDnet COST action workshop. Sanders C, Hall J, Sanders C, Dessens A, Bryce J, Callens N, Cools M, Kourime M, Kyriakou A, Springer A, Audi L, Balsamo A, Iotova V, Mladenov V, Krawczynski M, Nordenskjöld A, Rozas M, Claahsen-van der Grinten H, Hiort O, Riedl S, Ahmed SF. Sex Dev. 2018 Jun 23. doi: 10.1159/000490081. PMID: 29936513. https://www.ncbi.nlm.nih.gov/pubmed/29936513

• Diagnosis, treatment and prevention of pediatric obesity: consensus position statement of the Italian Society for Pediatric Endocrinology and Diabetology and the Italian Society of Pediatrics. Valerio G, Maffeis C, Saggese G, Ambruzzi MA, Balsamo A, Bellone S, Bergamini M, Bernasconi S, Bona G, Calcaterra V, Canali T, Caroli M, Chiarelli F, Corciulo N, Crinò A, Di Bonito P, Di Pietrantonio V, Di Pietro M, Di Sessa A, Diamanti A, Doria M, Fintini D, Franceschi R, Franzese A, Giussani M, Grugni G, Iafusco D, Iughetti L, Lamborghini A, Licenziati MR, Limauro R, Maltoni G, Manco M, Reggiani LM, Marcovecchio L, Marsciani A, Del Giudice EM, Morandi A, Morino G, Moro B, Nobili V, Perrone L, Picca M, Pietrobelli A, Privitera F, Purromuto S, Ragusa L, Ricotti R, Santamaria F, Sartori C, Stilli S, Street ME, Tanas R, Trifiró G, Umano GR, Vania A, Verduci E, Zito E. Ital J Pediatr. 2018 Jul 31;44(1):88. https://doi.org/10.1186/s13052-018-0525-6 Review. PMID:30064525

• Management of Gonads in Adults with Androgen Insensitivity: An International Survey. Tack LJW, Maris E, Looijenga LHJ, Hannema SE, Audi L, Köhler B, Holterhus PM, Riedl S, Wisniewski A, Flück CE, Davies JH, T Apos Sjoen G, Lucas-Herald AK, Evliyaoglu O, Krone N, Iotova V, Marginean O, Balsamo A, Verkauskas G, Weintrob, N, Ellaithi M, Nordenström A, Verrijn Stuart A, Kluivers KB, Wolffenbuttel KP, Ahmed SF, Cools M. Horm Res Paediatr. 2018 Oct 18:1-11. doi: 10.1159/000493645.. https://www.ncbi.nlm.nih.gov/pubmed/30336477
  PMID: 30336477

• Evaluation of DSD training schools organized by cost action BM1303 “DSDnet”. Bertalan R, Lucas-Herald A, Kolesinska Z, Berra M, Cools M, Balsamo A, Hiort O. Orphanet J Rare Dis. 2018 Dec 18;13(1):227. https://doi.org/10.1186/s13023-018-0967-3. PMID: 30563557

• Thyroid function in patients with Prader-Willi syndrome: an Italian multicenter study of 339 patients. Iughetti L, Vivi G, Balsamo A, Corrias A, Crinò A, Delvecchio M, Gargantini L, Greggio NA, Grugni G, Hladnik U, Pilotta A, Ragusa L, Salvatoni A, Wasniewska M, Weber G, Predieri B. J Pediatr Endocrinol Metab. 2019 Feb 25;32(2):159-165. https://doi.org/10.1515/jpem-2018-038

• Clinical but not histological outcomes in males with 45,X/46,XY mosaicism vary depending on reason for diagnosis.
  Ljubicic ML, Jørgensen A, Acerini C, Ribeiro de Andrade JG, Balsamo A, Bertelloni S, Cools M, Cuccaro RT, Darendeliler F, Flück CE, Grinspon RP, Maciel-Guerra A, Guran T, Hannema SE, Lucas-Herald AK, Hiort O, Holterhus PM, Lichiardopol C, Looijenga LHJ, Ortolano R, Riedl S, Ahmed SF, Juul A.  J Clin Endocrinol Metab. 2019 Apr 25. pii: jc.2018-02752. https://doi.org/10.1210/jc.2018-02752  PMID: 31127831.

• X-linked hypophosphatemic rickets: an Italian experts’ opinion survey. Emma F, Cappa M, Antoniazzi F, Bianchi ML, Chiodini I, Eller Vainicher C, Di Iorgi N, Maghnie M, Cassio A, Balsamo A, Baronio F, de Sanctis L, Tessaris D, Baroncelli GI, Mora S, Brandi ML, Weber G, D’Ausilio A, Lanati EP. Ital J Pediatr. 2019 May 31;45(1):67. https://doi.org/10.1186/s13052-019-0654-6. PMID:31151476

• Familial Neurohypophyseal Diabetes Insipidus in 13 kindreds and 2 Novel Mutations in the Vasopressin Gene.
  Patti G, Scianguetta S, Roberti D, Di Mascio A, Balsamo A, Brugnara M, Cappa M, Casale M, Cavarzere P, Cipriani S, Corbetta S, Gaudino R, Iughetti L, Martini L, Napoli F, Peri A, Salerno M, Salerno R, Passeri E, Maghnie M, Perrotta S, Di Iorgi N. Eur J Endocrinol. 2019 Jun 1. pii: EJE-19-0299.R2. https://doi.org/10.1530/EJE-19-0299   PMID: 31238300

• Response to Letter: “Clinical but not histological outcomes in males with 45,X/46,XY mosaicism vary depending on reason for diagnosis”. Ljubicic ML, Jørgensen A, Ribeiro de Andrade JG, Balsamo A, Bertelloni S, Cools M, Cuccaro RT, Darendeliler F, Flück CE, Grinspon RP, Maciel-Guerra A, Guran T, Hannema SE, Lucas-Herald AK, Hiort O, Holterhus PM, Lichiardopol C, Looijenga LHJ, Ortolano R, Riedl S, Ahmed SF, Juul A. J Clin Endocrinol Metab. 2019 Jul 5. pii:jc.2019-01413. https://doi.org/10.1210/jc.2019-01413  PMID: 31276168. Letter to the Editor: Clinical but not histological outcomes in males with 45,X/46,XY mosaicism vary depending on reason for diagnosis. Dumeige L, Martinerie L.   J Clin Endocrinol Metab. 2019 Jul 5. pii: jc.2019-01282. doi: 10.1210/jc.2019-01282. https://doi.org/10.1210/jc.2019-01282  PMID: 31276169

• Addressing gaps in care of people with conditions affecting sex development and maturation. Hiort O, Cools M, Springer A, McElreavey K, Greenfield A, Wudy SA, Kulle A, Ahmed SF, Dessens A, Balsamo A, Maghnie M, Bonomi M, Dattani M, Persani L, Audi L; COST Actions DSDnet and GnRH Network as well as the European Reference Network for Rare Endocrine Conditions (Endo–ERN). Nat Rev Endocrinol. 2019 Oct;15(10):615-622. https://doi.org/10.1038/s41574-019-0238-y  Epub 2019 Aug 12. Review. PMID: 31406344.

• Novel Non-Classic CYP21A2 Variants, Including Combined Alleles, Identified in Patients with Congenital Adrenal Hyperplasia. Karlsson L, de Paula Michelatto D, Lusa ALG, D’Almeida Mgnani Silva C, Östberg LJ, Persson B, Guerra-Júnior G, Valente de Lemos-Marini SH, Baldazzi L, Menabó S, Balsamo A, Greggio NA, Palandi de Mello M, Barbaro M, Lajic S. Clin Biochem. 2019 Jul 22. pii:S0009-9120(19)30457-6. https://doi.org/10.1016/j.clinbiochem.2019.07.009 PMID: 31344365.

• 46,XX DSD due to Androgen Excess in Monogenic Disorders of Steroidogenesis: Genetic, Biochemical, and Clinical Features. Baronio F, Ortolano R, Menabò S, Cassio A, Baldazzi L, Di Natale V, Tonti G, Vestrucci B, Balsamo A. Int J Mol Sci. 2019 Sep 17;20(18). pii: E4605.  https://doi.org/10.3390/ijms20184605. Review. PMID: 31533357.

• Plasma renin measurements are unrelated to mineralocorticoid replacement dose in patients with primary adrenal insufficiency. Pofi R, Prete A, Thornton-Jones V, Bryce J, Ali SR, Faisal Ahmed S, Balsamo A, Baronio F, Cannuccia A, Guven A, Guran T, Darendeliler F, Higham C, Bonfig W, de Vries L, Bachega TASS, Miranda MC, Mendonca BB, Iotova V, Korbonits M, Krone NP, Krone R, Lenzi A, Arlt W, Ross RJ, Isidori AM, Tomlinson JW.   J Clin Endocrinol Metab. 2019 Oct 16. pii: dgz055. https://doi.org/10.1210/clinem/dgz055 PMID: 31613957.

• Good overall behavioural adjustment in children and adolescents with classic congenital adrenal hyperplasia. Messina V, Hirvikoski T, Karlsson L, Vissani S, Wallensteen L, Ortolano R, Balsamo A, Nordenström A, Lajic L.E. Endocrine. 2020 Mar 9. https://doi.org/10.1007/s12020-020-02244-1 PMID: 32152914

• Growth Trajectory and Adult Height in Children with Nonclassical Congenital Adrenal Hyperplasia. Wasniewska MG, Morabito LA, Baronio F, Einaudi S, Salerno M, Bizzarri C, Russo G, Chiarito M, Grandone A, Guazzarotti L, Spinuzza A, Corica D, Ortolano R, Balsamo A, Abrigo E, Baldini Ferroli B, Alibrandi A, Capalbo D, Aversa T, Faienza MF; Adrenal Diseases Working Group of the Italian Society for Pediatric Endocrinology and Diabetology. Horm Res Paediatr 2020;93:173–181. https://doi.org/10.1159/000509548. PMID: 32810858

• Congenital Adrenal Hyperplasias Presenting in the Newborn and Young Infant. Balsamo A, Baronio F, Ortolano R, Menabo S, Baldazzi L, Di Natale V, Vissani S, Cassio A. Front Pediatr. 2020 Dec 22;8:593315. https://doi.org/10.3389/fped.2020.593315. PMID: 33415088; PMCID: PMC7783414.

• Real World Estimates Of Adrenal Insufficiency Related Adverse Events In Children With Congenital Adrenal Hyperplasia. Ali SR, Bryce J, Haghpanahan H, Lewsey JD, Tan LE, Atapattu N, Birkebaek NH, Blankenstein O, Neumann U, Balsamo A, Ortolano R, Bonfig W, Claahsen-van der Grinten HL, Cools M, Costa EC, Darendeliler F, Poyrazoglu S, Elsedfy H, Finken MJJ, Fluck CE, Gevers E, Korbonits M, Guaragna-Filho G, Guran T, Guven A, Hannema SE, Higham C, Hughes IA, Tadokoro-Cuccaro R, Thankamony A, Iotova V, Krone NP, Krone R, Lichiardopol C, Luczay A, Mendonca BB, Bachega TASS, Miranda MC, Milenkovic T, Mohnike K, Nordenstrom A, Einaudi S, van der Kamp H, Vieites A, de Vries L, Ross RJM, Ahmed SF. J Clin Endocrinol Metab 106:1, January 2021, Pages e192–e203,  https://doi.org/10.1210/clinem/dgaa694 . PMID: 32995889.

• Primary Adrenal Insufficiency in childhood: data from a large nationwide cohort. Capalbo D, Moracas C, Cappa M, Balsamo A, Maghnie M, Wasniewska MG, Greggio NA, Baronio F, Bizzarri C, Ferro G, Di Lascio A, Stancampiano MR, Azzolini S, Patti G, Longhi S, Valenzise M, Radetti G, Betterle C, Russo G, Salerno M. J Clin Endocrinol Metab. 2020 Nov 28:dgaa881. https://doi.org/10.1210/clinem/dgaa881 . PMID: 33247909.

• International practice of corticosteroid replacement therapy in congenital adrenal hyperplasia – data from the I-CAH registry. Irina Bacila¹, Oliver Blankenstein², Uta Neumann², Hedi L Claahsen – van der Grinten³, Ruth Krone⁴, Tania SS Bachega⁵, Mirella C Miranda⁵, Berenice Mendonca⁵, Niels H Birkebaek⁶, Martine Cools⁷, Tatjana Milenkovic⁸, Walter Bonfig^9,10, Jeremy Tomlinson¹¹, Heba Elsedfy¹², Antonio Balsamo¹³, Rita Ortolano¹³, Sabine Hannema^14,15, Claire Higham¹⁶, Navoda Atapattu¹⁷, Corina Lichiardopol¹⁸, Tulay Guran¹⁹, Zehra Abali¹⁹, Klaus Mohnike²⁰, Martijn JJ Finken²¹, Ana Vieites²², Feyza Darendeliler²³, Ayla Guven²⁴, Marta Korbonits²⁵, Liat de Vries^26,27, Eduardo Costa²⁸, Einaudi Silvia²⁹, Hetty van der Kamp³⁰, Violeta Iotova³¹, Richard Ross¹, S Faisal Ahmed³², Nils Krone¹. Eur J Endocrinol 2021, in press http://dx.doi.org/10.1530/EJE-20-1249

E’ membro delle seguenti società scientifiche nazionali/internazionali, comitati, board, ecc.

• Membro di Società Nazionali (SIP, SIEDP, SIRP, SIMMESN) ed Internazionali (ESPE) di Pediatria, Endocrinologia e Diabetologia Pediatrica