Salina A - Search Results

1

A Novel Genetic Variant in the WFS1 Gene in a Patient with Partial Uniparental Mero-Isodisomy of Chromosome 4.

Delvecchio M, Ortolani F, Palumbo O, Aloi C, Salina A, Susca FC, Palumbo P, Carella M, Resta N, Piccinno E. Delvecchio M, et al. Among authors: salina a. Int J Mol Sci. 2021 Jul 28;22(15):8082. doi: 10.3390/ijms22158082. Int J Mol Sci. 2021. PMID: 34360843 Free PMC article.

2

Estimation of genetic risk for Type 1 diabetes mellitus in newborns on dried blood spot.

Giannattasio A, Caruso U, Napoli F, Salina A, Aloi C, Lorini R, d'Annunzio G. Giannattasio A, et al. Among authors: salina a. J Endocrinol Invest. 2010 Jun;33(6):406-8. doi: 10.1007/BF03346612. Epub 2010 Jan 22. J Endocrinol Invest. 2010. PMID: 20101097

3

A novel hepatocyte nuclear factor-1β (MODY 5) gene mutation in a Romanian boy with pancreatic calcifications, renal and hepatic dysfunction.

Banin P, Giovannini M, Raimondi F, D'Annunzio G, Sala S, Salina A, Aloi C, De Sanctis V. Banin P, et al. Among authors: salina a. Georgian Med News. 2011 Apr;(193):55-60. Georgian Med News. 2011. PMID: 21617276

4

The coexistence of type 1 diabetes, MODY2 and metabolic syndrome in a young girl.

Calcaterra V, Martinetti M, Salina A, Aloi C, Larizza D. Calcaterra V, et al. Among authors: salina a. Acta Diabetol. 2012 Oct;49(5):401-4. doi: 10.1007/s00592-011-0300-2. Epub 2011 Jun 18. Acta Diabetol. 2012. PMID: 21688019

5

Mother and daughter carrying the same KCNJ11 mutation but with a different response to switching from insulin to sulfonylurea.

Russo C, Salina A, Aloi C, Iafusco D, Lorini R, d'Annunzio G. Russo C, et al. Among authors: salina a. Diabetes Res Clin Pract. 2011 Nov;94(2):e50-2. doi: 10.1016/j.diabres.2011.07.039. Epub 2011 Aug 25. Diabetes Res Clin Pract. 2011. PMID: 21871684

6

Wolfram syndrome: new mutations, different phenotype.

Aloi C, Salina A, Pasquali L, Lugani F, Perri K, Russo C, Tallone R, Ghiggeri GM, Lorini R, d'Annunzio G. Aloi C, et al. Among authors: salina a. PLoS One. 2012;7(1):e29150. doi: 10.1371/journal.pone.0029150. Epub 2012 Jan 4. PLoS One. 2012. PMID: 22238590 Free PMC article.

7

Hyperglycaemia and β-cell antibodies: is it always pre-type 1 diabetes?

d'Annunzio G, Marchi M, Aloi C, Salina A, Lugani F, Lorini R. d'Annunzio G, et al. Among authors: salina a. Diabetes Res Clin Pract. 2013 Apr;100(1):e20-2. doi: 10.1016/j.diabres.2013.01.003. Epub 2013 Jan 24. Diabetes Res Clin Pract. 2013. PMID: 23352578

8

Novel homozygous mutation in exon 5 of WFS1 gene in an Apulian family with mild phenotypic expression of Wolfram syndrome.

Piccinno E, Ortolani F, Vendemiale M, Tummolo A, Masciopinto M, Natale MP, De Luca A, Agolini E, Aloi C, Salina A, D'Annunzio G, Fischetto R, Papadia F. Piccinno E, et al. Among authors: salina a. Clin Genet. 2014 Aug;86(2):197-8. doi: 10.1111/cge.12260. Epub 2013 Oct 3. Clin Genet. 2014. PMID: 24117146 No abstract available.

9

A novel CISD2 intragenic deletion, optic neuropathy and platelet aggregation defect in Wolfram syndrome type 2.

Mozzillo E, Delvecchio M, Carella M, Grandone E, Palumbo P, Salina A, Aloi C, Buono P, Izzo A, D'Annunzio G, Vecchione G, Orrico A, Genesio R, Simonelli F, Franzese A. Mozzillo E, et al. Among authors: salina a. BMC Med Genet. 2014 Jul 24;15:88. doi: 10.1186/1471-2350-15-88. BMC Med Genet. 2014. PMID: 25056293 Free PMC article.

10

Monogenic Diabetes Accounts for 6.3% of Cases Referred to 15 Italian Pediatric Diabetes Centers During 2007 to 2012.

Delvecchio M, Mozzillo E, Salzano G, Iafusco D, Frontino G, Patera PI, Rabbone I, Cherubini V, Grasso V, Tinto N, Giglio S, Contreas G, Di Paola R, Salina A, Cauvin V, Tumini S, d'Annunzio G, Iughetti L, Mantovani V, Maltoni G, Toni S, Marigliano M, Barbetti F; Diabetes Study Group of the Italian Society of Pediatric Endocrinology and Diabetes (ISPED). Delvecchio M, et al. Among authors: salina a. J Clin Endocrinol Metab. 2017 Jun 1;102(6):1826-1834. doi: 10.1210/jc.2016-2490. J Clin Endocrinol Metab. 2017. PMID: 28323911

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