Colombo MG - Search Results

1

ET-1 Lys198Asn and ET(A) receptor H323H polymorphisms in heart failure. A case-control study.

Colombo MG, Ciofini E, Paradossi U, Bevilacqua S, Biagini A. Colombo MG, et al. Cardiology. 2006;105(4):246-52. doi: 10.1159/000092374. Epub 2006 Mar 30. Cardiology. 2006. PMID: 16582543

2

Weight is an independent predictor of vascular injury in healthy volunteers with aspartate allele.

Paradossi U, Manfrini O, Ciofini E, Pizzi C, Biagini A, Xhyheri B, Colombo MG. Paradossi U, et al. Among authors: colombo mg. J Cardiovasc Med (Hagerstown). 2012 May;13(5):307-12. doi: 10.2459/JCM.0b013e3283536a0a. J Cardiovasc Med (Hagerstown). 2012. PMID: 22450868

3

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. Among authors: colombo mg. Environ Mol Mutagen. 2002;40(2):110-5. doi: 10.1002/em.10098. Environ Mol Mutagen. 2002. PMID: 12203403

4

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: colombo mg. 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.

5

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. Clin Chem. 2003 Mar;49(3):389-95. doi: 10.1373/49.3.389. Clin Chem. 2003. PMID: 12600950 Free article.

6

Genetic polymorphisms in folate and homocysteine metabolism as risk factors for DNA damage.

Botto N, Andreassi MG, Manfredi S, Masetti S, Cocci F, Colombo MG, Storti S, Rizza A, Biagini A. Botto N, et al. Among authors: colombo mg. Eur J Hum Genet. 2003 Sep;11(9):671-8. doi: 10.1038/sj.ejhg.5201024. Eur J Hum Genet. 2003. PMID: 12939653

7

Endothelial function and carotid intima-media thickness in young healthy subjects among endothelial nitric oxide synthase Glu298-->Asp and T-786-->C polymorphisms.

Paradossi U, Ciofini E, Clerico A, Botto N, Biagini A, Colombo MG. Paradossi U, et al. Among authors: colombo mg. Stroke. 2004 Jun;35(6):1305-9. doi: 10.1161/01.STR.0000126482.86708.37. Epub 2004 Apr 8. Stroke. 2004. PMID: 15073390

8

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: colombo mg. Cardiovasc Ultrasound. 2010 Mar 22;8:9. doi: 10.1186/1476-7120-8-9. Cardiovasc Ultrasound. 2010. PMID: 20307303 Free PMC article.

9

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. Heart. 2002 Jun;87(6):525-8. doi: 10.1136/heart.87.6.525. Heart. 2002. PMID: 12010932 Free PMC article.

10

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: colombo mg. Hum Genet. 2003 Feb;112(2):171-7. doi: 10.1007/s00439-002-0859-3. Epub 2002 Nov 13. Hum Genet. 2003. PMID: 12522558

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