D'Amato E - Search Results

1

Collectrin gene screening in Turner syndrome patients with kidney malformation.

Pasquali L, d'Annunzio G, Gastaldi R, Di Battista E, Calcaterra V, Larizza D, Lorini R, D'Amato E. Pasquali L, et al. J Genet. 2009 Apr;88(1):105-8. doi: 10.1007/s12041-009-0015-0. J Genet. 2009. PMID: 19417552 No abstract available.

2

Horseshoe kidney malformation in Turner syndrome is not associated with HNF-1beta gene mutations.

D'Amato E, d'Annunzio G, Calcaterra V, Morsellino V, Larizza D, Lorini R. D'Amato E, et al. Pediatr Nephrol. 2008 Jan;23(1):137-40. doi: 10.1007/s00467-007-0609-9. Epub 2007 Oct 6. Pediatr Nephrol. 2008. PMID: 17922147

3

Wolfram syndrome (diabetes insipidus, diabetes, optic atrophy, and deafness): clinical and genetic study.

d'Annunzio G, Minuto N, D'Amato E, de Toni T, Lombardo F, Pasquali L, Lorini R. d'Annunzio G, et al. Diabetes Care. 2008 Sep;31(9):1743-5. doi: 10.2337/dc08-0178. Epub 2008 Jun 19. Diabetes Care. 2008. PMID: 18566338 Free PMC article.

4

Genetic investigation in an Italian child with an unusual association of atrial septal defect, attributable to a new familial GATA4 gene mutation, and neonatal diabetes due to pancreatic agenesis.

D'Amato E, Giacopelli F, Giannattasio A, D'Annunzio G, Bocciardi R, Musso M, Lorini R, Ravazzolo R. D'Amato E, et al. Diabet Med. 2010 Oct;27(10):1195-200. doi: 10.1111/j.1464-5491.2010.03046.x. Diabet Med. 2010. PMID: 20854389

5

Variable phenotypic spectrum of diabetes mellitus in a family carrying a novel KCNJ11 gene mutation.

D'Amato E, Tammaro P, Craig TJ, Tosi A, Giorgetti R, Lorini R, Ashcroft FM. D'Amato E, et al. Diabet Med. 2008 Jun;25(6):651-6. doi: 10.1111/j.1464-5491.2008.02443.x. Diabet Med. 2008. PMID: 18544102

6

Maturity-onset diabetes of the young in children with incidental hyperglycemia: a multicenter Italian study of 172 families.

Lorini R, Klersy C, d'Annunzio G, Massa O, Minuto N, Iafusco D, Bellannè-Chantelot C, Frongia AP, Toni S, Meschi F, Cerutti F, Barbetti F; Italian Society of Pediatric Endocrinology and Diabetology (ISPED) Study Group. Lorini R, et al. Diabetes Care. 2009 Oct;32(10):1864-6. doi: 10.2337/dc08-2018. Epub 2009 Jun 29. Diabetes Care. 2009. PMID: 19564454 Free PMC article.

7

Hyperglycemia in celiac disease: not always pretype 1 diabetes?

Ingegnosi C, Caruso-Nicoletti M, D'Amato E, d'Annunzio G, Lorini R. Ingegnosi C, et al. Pediatr Diabetes. 2008 Jul 28;9(4 Pt 1):335-7. doi: 10.1111/j.1399-5448.2008.00384.x. Pediatr Diabetes. 2008. PMID: 18768037

8

Letter Re: Neonatal diabetes mellitus and mutation in the HNF-1beta gene.

D'Amato E, Lorini R. D'Amato E, et al. J Clin Endocrinol Metab. 2005 Oct;90(10):5906-7. doi: 10.1210/jc.2005-1156. J Clin Endocrinol Metab. 2005. PMID: 16207896 No abstract available.

9

KCNJ11 activating mutations in Italian patients with permanent neonatal diabetes.

Massa O, Iafusco D, D'Amato E, Gloyn AL, Hattersley AT, Pasquino B, Tonini G, Dammacco F, Zanette G, Meschi F, Porzio O, Bottazzo G, Crinó A, Lorini R, Cerutti F, Vanelli M, Barbetti F; Early Onset Diabetes Study Group of the Italian Society of Pediatric Endocrinology and Diabetology. Massa O, et al. Hum Mutat. 2005 Jan;25(1):22-7. doi: 10.1002/humu.20124. Hum Mutat. 2005. PMID: 15580558

10

Enhanced glomerular Toll-like receptor 4 expression and signaling in patients with type 2 diabetic nephropathy and microalbuminuria.

Verzola D, Cappuccino L, D'Amato E, Villaggio B, Gianiorio F, Mij M, Simonato A, Viazzi F, Salvidio G, Garibotto G. Verzola D, et al. Kidney Int. 2014 Dec;86(6):1229-43. doi: 10.1038/ki.2014.116. Epub 2014 Apr 30. Kidney Int. 2014. PMID: 24786705 Free article.

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