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Klinefelter syndrome (KS): genetics, clinical phenotype and hypogonadism.
Bonomi M, Rochira V, Pasquali D, Balercia G, Jannini EA, Ferlin A; Klinefelter ItaliaN Group (KING). Bonomi M, et al. Among authors: ferlin a. J Endocrinol Invest. 2017 Feb;40(2):123-134. doi: 10.1007/s40618-016-0541-6. Epub 2016 Sep 19. J Endocrinol Invest. 2017. PMID: 27644703 Free PMC article. Review.
Spermatogenesis in Klinefelter syndrome.
Selice R, Di Mambro A, Garolla A, Ficarra V, Iafrate M, Ferlin A, Foresta C. Selice R, et al. Among authors: ferlin a. J Endocrinol Invest. 2010 Dec;33(11):789-93. doi: 10.1007/BF03350343. Epub 2010 Mar 22. J Endocrinol Invest. 2010. PMID: 20332707
Osteoporosis in Klinefelter's syndrome.
Ferlin A, Schipilliti M, Di Mambro A, Vinanzi C, Foresta C. Ferlin A, et al. Mol Hum Reprod. 2010 Jun;16(6):402-10. doi: 10.1093/molehr/gaq026. Epub 2010 Mar 27. Mol Hum Reprod. 2010. PMID: 20348548 Review.
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.
Reduced artery diameters in Klinefelter syndrome.
Foresta C, Caretta N, Palego P, Ferlin A, Zuccarello D, Lenzi A, Selice R. Foresta C, et al. Among authors: ferlin a. Int J Androl. 2012 Oct;35(5):720-5. doi: 10.1111/j.1365-2605.2012.01269.x. Epub 2012 Apr 10. Int J Androl. 2012. PMID: 22489599
Y-chromosome microdeletions are not associated with SHOX haploinsufficiency.
Chianese C, Lo Giacco D, Tüttelmann F, Ferlin A, Ntostis P, Vinci S, Balercia G, Ars E, Ruiz-Castañé E, Giglio S, Forti G, Kliesch S, Krausz C. Chianese C, et al. Among authors: ferlin a. Hum Reprod. 2013 Nov;28(11):3155-60. doi: 10.1093/humrep/det322. Epub 2013 Sep 5. Hum Reprod. 2013. PMID: 24008148
Germline prokineticin receptor 2 (PROKR2) variants associated with central hypogonadism cause differental modulation of distinct intracellular pathways.
Libri DV, Kleinau G, Vezzoli V, Busnelli M, Guizzardi F, Sinisi AA, Pincelli AI, Mancini A, Russo G, Beck-Peccoz P, Loche S, Crivellaro C, Maghnie M, Krausz C, Persani L, Bonomi M; Italian Study Group on Idiopathic Central Hypogonadism (ICH). Libri DV, et al. J Clin Endocrinol Metab. 2014 Mar;99(3):E458-63. doi: 10.1210/jc.2013-2431. Epub 2013 Nov 25. J Clin Endocrinol Metab. 2014. PMID: 24276467 Free article.
Reply: Y-chromosome microdeletions are not associated with SHOX haploinsufficiency.
Krausz C, Chianese C, Lo Giacco D, Tüttelmann F, Ferlin A, Ntostis P, Vinci S, Balercia G, Ars E, Ruiz-Castañé E, Giglio S, Kliesch S, Forti G. Krausz C, et al. Among authors: ferlin a. Hum Reprod. 2014 May;29(5):1114-5. doi: 10.1093/humrep/deu037. Epub 2014 Mar 14. Hum Reprod. 2014. PMID: 24634250 No abstract available.
311 results