Vittorini S - Search Results

1

[Genetic screening of Gata4 and Nkx2.5 mutations in hereditary congenital heart defects: 5 familial cases].

Pulignani S, Foffa I, Cresci M, Vittorini S, Ait-Ali L, Andreassi MG. Pulignani S, et al. Among authors: vittorini s. Recenti Prog Med. 2011 Mar;102(3):120-5. doi: 10.1701/608.7068. Recenti Prog Med. 2011. PMID: 21572484 Italian.

2

Clinical utility of genetic tests for inherited hypertrophic and dilated cardiomyopathies.

Colombo MG, Botto N, Vittorini S, Paradossi U, Andreassi MG. Colombo MG, et al. Among authors: vittorini s. Cardiovasc Ultrasound. 2008 Dec 19;6:62. doi: 10.1186/1476-7120-6-62. Cardiovasc Ultrasound. 2008. PMID: 19099557 Free PMC article. Review.

3

A novel LMNA mutation (R189W) in familial dilated cardiomyopathy: evidence for a 'hot spot' region at exon 3: a case report.

Botto N, Vittorini S, Colombo MG, Biagini A, Paradossi U, Aquaro G, Andreassi MG. Botto N, et al. Among authors: vittorini s. Cardiovasc Ultrasound. 2010 Mar 22;8:9. doi: 10.1186/1476-7120-8-9. Cardiovasc Ultrasound. 2010. PMID: 20307303 Free PMC article.

4

[A novel lamin A/C mutation in a family with dilated cardiomyopathy and a strong history of sudden cardiac death].

Andreassi MG, Botto N, Vittorini S, Pulignani S, Aquaro G, Sicari R. Andreassi MG, et al. Among authors: vittorini s. Recenti Prog Med. 2010 Mar;101(3):127-30. Recenti Prog Med. 2010. PMID: 20461955 Italian.

5

A novel TGFβR2 splice variant in patient with aortic aneurysm and family history for aortic dissection: a case report.

Vecoli C, Foffa I, Vittorini S, Botto N, Esposito A, Costa S, Piagneri V, Festa P, Ait-Ali L. Vecoli C, et al. Among authors: vittorini s. Per Med. 2024;21(3):139-144. doi: 10.2217/pme-2023-0135. Epub 2024 Apr 18. Per Med. 2024. PMID: 38634413

6

SERCA2a, phospholamban, sarcolipin, and ryanodine receptors gene expression in children with congenital heart defects.

Vittorini S, Storti S, Parri MS, Cerillo AG, Clerico A. Vittorini S, et al. Mol Med. 2007 Jan-Feb;13(1-2):105-11. doi: 10.2119/2006-00054.Vittorini. Mol Med. 2007. PMID: 17515962 Free PMC article.

7

The neuroendocrinal system of the heart after construction of a Glenn anastomosis or the Fontan circulation.

Vittorini S, Storti S, Parri MS, Moschetti R, Scebba L, Clerico A, Murzi B, Luisi VS. Vittorini S, et al. Cardiol Young. 2005 Dec;15 Suppl 3:21-5. doi: 10.1017/S1047951105001587. Cardiol Young. 2005. PMID: 16248920 No abstract available.

8

Polymorphisms in the eNOS gene and the risk of coronary artery disease: Making the case for genome-wide association studies.

Aimo A, Botto N, Vittorini S, Emdin M. Aimo A, et al. Among authors: vittorini s. Eur J Prev Cardiol. 2019 Jan;26(2):157-159. doi: 10.1177/2047487318797402. Epub 2018 Aug 30. Eur J Prev Cardiol. 2019. PMID: 30160177 No abstract available.

9

Molecular Autopsy of Sudden Cardiac Death in the Genomics Era.

Castiglione V, Modena M, Aimo A, Chiti E, Botto N, Vittorini S, Guidi B, Vergaro G, Barison A, Rossi A, Passino C, Giannoni A, Di Paolo M, Emdin M. Castiglione V, et al. Among authors: vittorini s. Diagnostics (Basel). 2021 Jul 30;11(8):1378. doi: 10.3390/diagnostics11081378. Diagnostics (Basel). 2021. PMID: 34441312 Free PMC article. Review.

10

A rapid procedure for the quantitation of natriuretic peptide RNAs by competitive RT-PCR in congenital heart defects.

Iascone MR, Vittorini S, Collavoli A, Cupelli A, Kraft G, Biagini A, Clerico A. Iascone MR, et al. Among authors: vittorini s. J Endocrinol Invest. 1999 Dec;22(11):835-42. doi: 10.1007/BF03343655. J Endocrinol Invest. 1999. PMID: 10710270

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