Manfredi S - Search Results

1

Evidence for association of a common variant of the endothelial nitric oxide synthase gene (Glu298-->Asp polymorphism) to the presence, extent, and severity of coronary artery disease.

Colombo MG, Andreassi MG, Paradossi U, Botto N, Manfredi S, Masetti S, Rossi G, Clerico A, Biagini A. Colombo MG, et al. Among authors: manfredi s. Heart. 2002 Jun;87(6):525-8. doi: 10.1136/heart.87.6.525. Heart. 2002. PMID: 12010932 Free PMC article.

2

P53 codon 72 polymorphism in coronary artery disease: no evidence for association with increased risk or micronucleus frequency.

Manfredi S, Masetti S, Botto N, Colombo MG, Terrazzi M, Vassalle C, Biagini A, Andreassi MG. Manfredi S, et al. Environ Mol Mutagen. 2002;40(2):110-5. doi: 10.1002/em.10098. Environ Mol Mutagen. 2002. PMID: 12203403

3

Methylenetetrahydrofolate reductase gene C677T polymorphism, homocysteine, vitamin B12, and DNA damage in coronary artery disease.

Andreassi MG, Botto N, Cocci F, Battaglia D, Antonioli E, Masetti S, Manfredi S, Colombo MG, Biagini A, Clerico A. Andreassi MG, et al. Among authors: manfredi s. Hum Genet. 2003 Feb;112(2):171-7. doi: 10.1007/s00439-002-0859-3. Epub 2002 Nov 13. Hum Genet. 2003. PMID: 12522558

4

Endothelial nitric oxide synthase gene polymorphisms and risk of coronary artery disease.

Colombo MG, Paradossi U, Andreassi MG, Botto N, Manfredi S, Masetti S, Biagini A, Clerico A. Colombo MG, et al. Among authors: manfredi s. Clin Chem. 2003 Mar;49(3):389-95. doi: 10.1373/49.3.389. Clin Chem. 2003. PMID: 12600950 Free article.

5

Detection of mtDNA with 4977 bp deletion in blood cells and atherosclerotic lesions of patients with coronary artery disease.

Botto N, Berti S, Manfredi S, Al-Jabri A, Federici C, Clerico A, Ciofini E, Biagini A, Andreassi MG. Botto N, et al. Among authors: manfredi s. Mutat Res. 2005 Feb 15;570(1):81-8. doi: 10.1016/j.mrfmmm.2004.10.003. Mutat Res. 2005. PMID: 15680405

6

GSTM1, GSTT1 and CYP1A1 detoxification gene polymorphisms and susceptibility to smoking-related coronary artery disease: a case-only study.

Manfredi S, Federici C, Picano E, Botto N, Rizza A, Andreassi MG. Manfredi S, et al. Mutat Res. 2007 Aug 1;621(1-2):106-12. doi: 10.1016/j.mrfmmm.2007.02.014. Epub 2007 Mar 2. Mutat Res. 2007. PMID: 17408703

7

Glutathione S-transferase T1- and M1-null genotypes and coronary artery disease risk in patients with Type 2 diabetes mellitus.

Manfredi S, Calvi D, del Fiandra M, Botto N, Biagini A, Andreassi MG. Manfredi S, et al. Pharmacogenomics. 2009 Jan;10(1):29-34. doi: 10.2217/14622416.10.1.29. Pharmacogenomics. 2009. PMID: 19102712

8

Evidence for DNA damage in patients with coronary artery disease.

Botto N, Rizza A, Colombo MG, Mazzone AM, Manfredi S, Masetti S, Clerico A, Biagini A, Andreassi MG. Botto N, et al. Among authors: manfredi s. Mutat Res. 2001 Jun 27;493(1-2):23-30. doi: 10.1016/s1383-5718(01)00162-0. Mutat Res. 2001. PMID: 11516712

9

Deoxyribonucleic acid damage in human lymphocytes after percutaneous transluminal coronary angioplasty.

Andreassi MG, Botto N, Rizza A, Colombo MG, Palmieri C, Berti S, Manfredi S, Masetti S, Clerico A, Biagini A. Andreassi MG, et al. Among authors: manfredi s. J Am Coll Cardiol. 2002 Sep 4;40(5):862-8. doi: 10.1016/s0735-1097(02)02042-9. J Am Coll Cardiol. 2002. PMID: 12225708 Free article.

10

Elevated levels of oxidative DNA damage in patients with coronary artery disease.

Botto N, Masetti S, Petrozzi L, Vassalle C, Manfredi S, Biagini A, Andreassi MG. Botto N, et al. Among authors: manfredi s. Coron Artery Dis. 2002 Aug;13(5):269-74. doi: 10.1097/00019501-200208000-00004. Coron Artery Dis. 2002. PMID: 12394651

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