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Year Number of Results
1989 1
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2005 2
2006 2
2007 1
2008 1
2009 3
2010 3
2011 5
2012 2
2013 1
2014 6
2015 7
2016 2
2017 4
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2020 7
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2022 9
2023 2
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56 results

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Page 1
A novel mutation in GCK gene: Beware of SGA child with diabetic mother.
Tagliaferri F, Grosso C, Balbo M, Bracciolini G, Bertelli E, Secco A, Salina A, Aloi C, Gallo M, Felici E. Tagliaferri F, et al. Among authors: secco a. Diabetes Res Clin Pract. 2021 Nov;181:109081. doi: 10.1016/j.diabres.2021.109081. Epub 2021 Oct 8. Diabetes Res Clin Pract. 2021. PMID: 34627944
Characteristics of a nationwide cohort of patients presenting with isolated hypogonadotropic hypogonadism (IHH).
Bonomi M, Vezzoli V, Krausz C, Guizzardi F, Vezzani S, Simoni M, Bassi I, Duminuco P, Di Iorgi N, Giavoli C, Pizzocaro A, Russo G, Moro M, Fatti L, Ferlin A, Mazzanti L, Zatelli MC, Cannavò S, Isidori AM, Pincelli AI, Prodam F, Mancini A, Limone P, Tanda ML, Gaudino R, Salerno M, Francesca P, Maghnie M, Maggi M, Persani L; Italian Network on Central Hypogonadism; Italian Network on Central Hypogonadism (NICe group). Bonomi M, et al. Eur J Endocrinol. 2018 Jan;178(1):23-32. doi: 10.1530/EJE-17-0065. Epub 2017 Sep 7. Eur J Endocrinol. 2018. PMID: 28882981 Free article.
Real-life long-term efficacy and safety of recombinant human growth hormone therapy in children with short stature homeobox-containing deficiency.
Bruzzi P, Vannelli S, Scarano E, Di Iorgi N, Parpagnoli M, Salerno M, Pitea M, Elisabeth Street M, Secco A, Andrea Trettene A, Wasniewska M, Corciulo N, Tornese G, Felicia Faienza M, Delvecchio M, Filomena Madeo S, Iughetti L. Bruzzi P, et al. Among authors: secco a. Endocr Connect. 2023 Jun 8;12(7):e220402. doi: 10.1530/EC-22-0402. Print 2023 Jul 1. Endocr Connect. 2023. PMID: 37014306 Free PMC article.
New understandings of the genetic basis of isolated idiopathic central hypogonadism.
Bonomi M, Libri DV, Guizzardi F, Guarducci E, Maiolo E, Pignatti E, Asci R, Persani L; Idiopathic Central Hypogonadism Study Group of the Italian Societies of Endocrinology and Pediatric Endocrinology and Diabetes. Bonomi M, et al. Asian J Androl. 2012 Jan;14(1):49-56. doi: 10.1038/aja.2011.68. Epub 2011 Dec 5. Asian J Androl. 2012. PMID: 22138902 Free PMC article. Review.
Novel Pathogenetic Variants in PTHLH and TRPS1 Genes Causing Syndromic Brachydactyly.
Elli FM, Mattinzoli D, Lucca C, Piu M, Maffini MA, Costanza J, Fontana L, Santaniello C, Forino C, Milani D, Bonati MT, Secco A, Gastaldi R, Alfieri C, Messa P, Miozzo M, Arosio M, Mantovani G. Elli FM, et al. Among authors: secco a. J Bone Miner Res. 2022 Mar;37(3):465-474. doi: 10.1002/jbmr.4490. Epub 2022 Jan 17. J Bone Miner Res. 2022. PMID: 34897794 Free PMC article.
56 results