Giusti B - Search Results

1

Two-Dimensional Aortic Size Normalcy: A Novelty Detection Approach.

Frasconi P, Baracchi D, Giusti B, Kura A, Spaziani G, Cherubini A, Favilli S, Di Lenarda A, Pepe G, Nistri S. Frasconi P, et al. Among authors: giusti b. Diagnostics (Basel). 2021 Feb 2;11(2):220. doi: 10.3390/diagnostics11020220. Diagnostics (Basel). 2021. PMID: 33540834 Free PMC article.

2

A major involvement of the cardiovascular system in patients affected by Marfan syndrome: novel mutations in fibrillin 1 gene.

Pepe G, Giusti B, Attanasio M, Comeglio P, Porciani MC, Giurlani L, Montesi GF, Calamai GC, Vaccari M, Favilli S, Abbate R, Gensini GF. Pepe G, et al. Among authors: giusti b. J Mol Cell Cardiol. 1997 Jul;29(7):1877-84. doi: 10.1006/jmcc.1997.0426. J Mol Cell Cardiol. 1997. PMID: 9236141

3

High prevalence of mild hyperhomocysteinemia in patients with abdominal aortic aneurysm.

Brunelli T, Prisco D, Fedi S, Rogolino A, Farsi A, Marcucci R, Giusti B, Pratesi C, Pulli R, Gensini GF, Abbate R, Pepe G. Brunelli T, et al. Among authors: giusti b. J Vasc Surg. 2000 Sep;32(3):531-6. doi: 10.1067/mva.2000.107563. J Vasc Surg. 2000. PMID: 10957660 Free article.

4

The C677T methylenetetrahydrofolate reductase mutation is not associated with Alzheimer's disease.

Brunelli T, Bagnoli S, Giusti B, Nacmias B, Pepe G, Sorbi S, Abbate R. Brunelli T, et al. Among authors: giusti b. Neurosci Lett. 2001 Nov 23;315(1-2):103-5. doi: 10.1016/s0304-3940(01)02316-3. Neurosci Lett. 2001. PMID: 11711225

5

Phenotypic variability of cardiovascular manifestations in Marfan Syndrome. Possible role of hyperhomocysteinemia and C677T MTHFR gene polymorphism.

Giusti B, Porciani MC, Brunelli T, Evangelisti L, Fedi S, Gensini GF, Abbate R, Sani G, Yacoub M, Pepe G. Giusti B, et al. Eur Heart J. 2003 Nov;24(22):2038-45. doi: 10.1016/j.ehj.2003.08.020. Eur Heart J. 2003. PMID: 14613740

6

Relevance of post-methionine homocysteine and lipoprotein (a) in evaluating the cardiovascular risk in young CAD patients.

Marcucci R, Brunelli T, Fedi S, Pepe G, Giusti B, Gori AM, Prisco D, Falai M, Margheri M, Abbate R, Gensini GF. Marcucci R, et al. Among authors: giusti b. Eur J Clin Invest. 2005 Jan;35(1):1-7. doi: 10.1111/j.1365-2362.2005.01439.x. Eur J Clin Invest. 2005. PMID: 15638812

7

Role of hyperhomocysteinemia in aortic disease.

Giusti B, Marcucci R, Lapini I, Sestini I, Lenti M, Yacoub M, Pepe G. Giusti B, et al. Cell Mol Biol (Noisy-le-grand). 2004 Dec;50(8):945-52. Cell Mol Biol (Noisy-le-grand). 2004. PMID: 15704258 Review.

8

An expanding role of biomarkers in acute aortic syndromes.

Pepe G, Giusti B, Yacoub M. Pepe G, et al. Among authors: giusti b. Clin Cardiol. 2006 Oct;29(10):432-3. doi: 10.1002/clc.4960291003. Clin Cardiol. 2006. PMID: 17063945 Free PMC article. No abstract available.

9

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. Among authors: giusti b. Mol Vis. 2007 Nov 29;13:2242-7. Mol Vis. 2007. PMID: 18087243

10

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. Among authors: giusti b. BMC Med Genet. 2014 Feb 24;15:23. doi: 10.1186/1471-2350-15-23. BMC Med Genet. 2014. PMID: 24564502 Free PMC article.

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