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Page 1
Genetic analysis of Italian patients with congenital hyperinsulinism of infancy.
Sogno Valin P, Proverbio MC, Diceglie C, Gessi A, di Candia S, Mariani B, Zamproni I, Mangano E, Asselta R, Battaglia C, Caruso-Nicoletti M, Mora S, Salvatoni A. Sogno Valin P, et al. Among authors: di candia s. Horm Res Paediatr. 2013;79(4):236-42. doi: 10.1159/000350827. Epub 2013 May 1. Horm Res Paediatr. 2013. PMID: 23652837
Whole genome SNP genotyping and exome sequencing reveal novel genetic variants and putative causative genes in congenital hyperinsulinism.
Proverbio MC, Mangano E, Gessi A, Bordoni R, Spinelli R, Asselta R, Valin PS, Di Candia S, Zamproni I, Diceglie C, Mora S, Caruso-Nicoletti M, Salvatoni A, De Bellis G, Battaglia C. Proverbio MC, et al. Among authors: di candia s. PLoS One. 2013 Jul 15;8(7):e68740. doi: 10.1371/journal.pone.0068740. Print 2013. PLoS One. 2013. PMID: 23869231 Free PMC article.
[Hyperinsuline hypoglycemias].
Chiumello G, Bosio L, Di Candia S, Sogno Valin P. Chiumello G, et al. Among authors: di candia s. Minerva Pediatr. 2007 Oct;59(5):547. Minerva Pediatr. 2007. PMID: 17947913 Italian. No abstract available.
POI: a score to modulate GH treatment in children with Prader-Willi syndrome.
Salvatoni A, Berini J, Chiumello G, Crinò A, Di Candia S, Gargantini L, Grugni G, Iughetti L, Luce A, Musolino G, Sogno Valin P, Spica Russotto V, Trifirò G. Salvatoni A, et al. Among authors: di candia s. Horm Res Paediatr. 2012;78(3):201-2. doi: 10.1159/000342649. Epub 2012 Sep 11. Horm Res Paediatr. 2012. PMID: 22986481 No abstract available.
Assessment of central adrenal insufficiency in children and adolescents with Prader-Willi syndrome.
Corrias A, Grugni G, Crinò A, Di Candia S, Chiabotto P, Cogliardi A, Chiumello G, De Medici C, Spera S, Gargantini L, Iughetti L, Luce A, Mariani B, Ragusa L, Salvatoni A, Andrulli S, Mussa A, Beccaria L; Study Group for Genetic Obesity of Italian Society of Pediatric Endocrinology and Diabetology (SIEDP/ISPED). Corrias A, et al. Among authors: di candia s. Clin Endocrinol (Oxf). 2012 Jun;76(6):843-50. doi: 10.1111/j.1365-2265.2011.04313.x. Clin Endocrinol (Oxf). 2012. PMID: 22150958
Disorders of glucose metabolism in Prader-Willi syndrome: Results of a multicenter Italian cohort study.
Fintini D, Grugni G, Bocchini S, Brufani C, Di Candia S, Corrias A, Delvecchio M, Salvatoni A, Ragusa L, Greggio N, Franzese A, Scarano E, Trifirò G, Mazzanti L, Chiumello G, Cappa M, Crinò A; Genetic Obesity Study Group of the Italian Society of Pediatric Endocrinology and Diabetology (ISPED). Fintini D, et al. Among authors: di candia s. Nutr Metab Cardiovasc Dis. 2016 Sep;26(9):842-7. doi: 10.1016/j.numecd.2016.05.010. Epub 2016 Jun 3. Nutr Metab Cardiovasc Dis. 2016. PMID: 27381990
Central adrenal insufficiency in young adults with Prader-Willi syndrome.
Grugni G, Beccaria L, Corrias A, Crinò A, Cappa M, De Medici C, Di Candia S, Gargantini L, Ragusa L, Salvatoni A, Sartorio A, Spera S, Andrulli S, Chiumello G, Mussa A; Genetic Obesity Study Group of the Italian Society of Pediatric Endocrinology and Diabetology (ISPED). Grugni G, et al. Among authors: di candia s. Clin Endocrinol (Oxf). 2013 Sep;79(3):371-8. doi: 10.1111/cen.12150. Epub 2013 May 11. Clin Endocrinol (Oxf). 2013. PMID: 23311724
25 results