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Congenital hyperinsulinism and glucose hypersensitivity in homozygous and heterozygous carriers of Kir6.2 (KCNJ11) mutation V290M mutation: K(ATP) channel inactivation mechanism and clinical management.
Loechner KJ, Akrouh A, Kurata HT, Dionisi-Vici C, Maiorana A, Pizzoferro M, Rufini V, de Ville de Goyet J, Colombo C, Barbetti F, Koster JC, Nichols CG. Loechner KJ, et al. Among authors: pizzoferro m. Diabetes. 2011 Jan;60(1):209-17. doi: 10.2337/db10-0731. Epub 2010 Oct 27. Diabetes. 2011. PMID: 20980454 Free PMC article.
Focal congenital hyperinsulinism managed by medical treatment: a diagnostic algorithm based on molecular genetic screening.
Maiorana A, Barbetti F, Boiani A, Rufini V, Pizzoferro M, Francalanci P, Faletra F, Nichols CG, Grimaldi C, de Ville de Goyet J, Rahier J, Henquin JC, Dionisi-Vici C. Maiorana A, et al. Among authors: pizzoferro m. Clin Endocrinol (Oxf). 2014 Nov;81(5):679-88. doi: 10.1111/cen.12400. Epub 2014 Jan 30. Clin Endocrinol (Oxf). 2014. PMID: 24383515
Cystic fibrosis: a surgical matter?
Caldaro T, Alghisi F, De Angelis P, Garganese MC, Rea F, Pizzoferro M, Villani MF, Romeo EF, Torroni F, Foschia F, Gambitta RA, Federici G, Lucidi V, Dall'Oglio L. Caldaro T, et al. Among authors: pizzoferro m. J Pediatr Surg. 2014 May;49(5):753-8. doi: 10.1016/j.jpedsurg.2014.02.089. Epub 2014 Mar 29. J Pediatr Surg. 2014. PMID: 24851763
22 results