Pepe G - Search Results

1

Role of TGFBR1 and TGFBR2 genetic variants in Marfan syndrome.

De Cario R, Sticchi E, Lucarini L, Attanasio M, Nistri S, Marcucci R, Pepe G, Giusti B. De Cario R, et al. Among authors: pepe g. J Vasc Surg. 2018 Jul;68(1):225-233.e5. doi: 10.1016/j.jvs.2017.04.071. Epub 2017 Aug 26. J Vasc Surg. 2018. PMID: 28847661 Free article.

2

Identification of fibrillin 1 gene mutations in patients with bicuspid aortic valve (BAV) without Marfan syndrome.

Pepe G, Nistri S, Giusti B, Sticchi E, Attanasio M, Porciani C, Abbate R, Bonow RO, Yacoub M, Gensini GF. Pepe G, et al. BMC Med Genet. 2014 Feb 24;15:23. doi: 10.1186/1471-2350-15-23. BMC Med Genet. 2014. PMID: 24564502 Free PMC article.

3

Marfan syndrome: current perspectives.

Pepe G, Giusti B, Sticchi E, Abbate R, Gensini GF, Nistri S. Pepe G, et al. Appl Clin Genet. 2016 May 9;9:55-65. doi: 10.2147/TACG.S96233. eCollection 2016. Appl Clin Genet. 2016. PMID: 27274304 Free PMC article. Review.

4

Differential Diagnosis between Marfan Syndrome and Loeys-Dietz Syndrome Type 4: A Novel Chromosomal Deletion Covering TGFB2.

Nistri S, De Cario R, Sticchi E, Spaziani G, Della Monica M, Giglio S, Favilli S, Giusti B, Stefano P, Pepe G. Nistri S, et al. Among authors: pepe g. Genes (Basel). 2021 Sep 22;12(10):1462. doi: 10.3390/genes12101462. Genes (Basel). 2021. PMID: 34680857 Free PMC article.

5

Bicuspid Aortic Valve: Role of Multiple Gene Variants in Influencing the Clinical Phenotype.

Sticchi E, De Cario R, Magi A, Giglio S, Provenzano A, Nistri S, Pepe G, Giusti B. Sticchi E, et al. Among authors: pepe g. Biomed Res Int. 2018 Sep 5;2018:8386123. doi: 10.1155/2018/8386123. eCollection 2018. Biomed Res Int. 2018. PMID: 30255099 Free PMC article.

6

FBN1 mutation screening of patients with Marfan syndrome and related disorders: detection of 46 novel FBN1 mutations.

Attanasio M, Lapini I, Evangelisti L, Lucarini L, Giusti B, Porciani M, Fattori R, Anichini C, Abbate R, Gensini G, Pepe G. Attanasio M, et al. Among authors: pepe g. Clin Genet. 2008 Jul;74(1):39-46. doi: 10.1111/j.1399-0004.2008.01007.x. Epub 2008 Apr 22. Clin Genet. 2008. PMID: 18435798

7

Is ectopia lentis in some cases a mild phenotypic expression of Marfan syndrome? Need for a long-term follow-up.

Pepe G, Lapini I, Evangelisti L, Attanasio M, Giusti B, Lucarini L, Fattori R, Pellicanò G, Scrivanti M, Porciani MC, Abbate R, Gensini GF. Pepe G, et al. Mol Vis. 2007 Nov 29;13:2242-7. Mol Vis. 2007. PMID: 18087243

8

ACE and TGFBR1 genes interact in influencing the susceptibility to abdominal aortic aneurysm.

Lucarini L, Sticchi E, Sofi F, Pratesi G, Pratesi C, Pulli R, Gensini GF, Abbate R, Pepe G, Fatini C. Lucarini L, et al. Among authors: pepe g. Atherosclerosis. 2009 Jan;202(1):205-10. doi: 10.1016/j.atherosclerosis.2008.04.038. Epub 2008 Apr 29. Atherosclerosis. 2009. PMID: 18550062

9

A Case Based Approach to Clinical Genetics of Thoracic Aortic Aneurysm/Dissection.

Giusti B, Nistri S, Sticchi E, De Cario R, Abbate R, Gensini GF, Pepe G. Giusti B, et al. Among authors: pepe g. Biomed Res Int. 2016;2016:9579654. doi: 10.1155/2016/9579654. Epub 2016 May 25. Biomed Res Int. 2016. PMID: 27314043 Free PMC article. Review.

10

Another piece in the puzzle of bicuspid aortic valve syndrome.

Nistri S, Giusti B, Pepe G, Cademartiri F. Nistri S, et al. Among authors: pepe g. Eur Heart J Cardiovasc Imaging. 2016 Nov;17(11):1248-1249. doi: 10.1093/ehjci/jew169. Epub 2016 Aug 7. Eur Heart J Cardiovasc Imaging. 2016. PMID: 27502291 Free PMC article. No abstract available.

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