Ferraresi P - Search Results

1

Modulation of factor VII levels by intron 7 polymorphisms: population and in vitro studies.

Pinotti M, Toso R, Girelli D, Bindini D, Ferraresi P, Papa ML, Corrocher R, Marchetti G, Bernardi F. Pinotti M, et al. Among authors: ferraresi p. Blood. 2000 Jun 1;95(11):3423-8. Blood. 2000. PMID: 10828024 Free article.

2

Mutation pattern in clinically asymptomatic coagulation factor VII deficiency.

Bernardi F, Castaman G, Pinotti M, Ferraresi P, Di Iasio MG, Lunghi B, Rodeghiero F, Marchetti G. Bernardi F, et al. Among authors: ferraresi p. Hum Mutat. 1996;8(2):108-15. doi: 10.1002/(SICI)1098-1004(1996)8:2<108::AID-HUMU2>3.0.CO;2-7. Hum Mutat. 1996. PMID: 8844208

3

Asymptomatic carriership of factor V Leiden and genotypes of the fibrinogen gene cluster.

Marchetti G, Ferraresi P, Legnani C, Pinotti M, Lunghi B, Scapoli C, Gemmati D, Coccheri S, Palareti G, Bernardi F. Marchetti G, et al. Among authors: ferraresi p. Br J Haematol. 2003 May;121(4):632-8. doi: 10.1046/j.1365-2141.2003.04339.x. Br J Haematol. 2003. PMID: 12752105 Free article.

4

Influence of polymorphisms in the factor VII gene promoter on activated factor VII levels and on the risk of myocardial infarction in advanced coronary atherosclerosis.

Bozzini C, Girelli D, Bernardi F, Ferraresi P, Olivieri O, Pinotti M, Martinelli N, Manzato F, Friso S, Villa G, Pizzolo F, Beltrame F, Corrocher R. Bozzini C, et al. Among authors: ferraresi p. Thromb Haemost. 2004 Sep;92(3):541-9. doi: 10.1160/TH04-02-0130. Thromb Haemost. 2004. PMID: 15351850

5

Increased factor VIII coagulant activity levels in male carriers of the factor V R2 polymorphism.

Martinelli N, Girelli D, Ferraresi P, Olivieri O, Lunghi B, Manzato F, Corrocher R, Bernardi F. Martinelli N, et al. Among authors: ferraresi p. Blood Coagul Fibrinolysis. 2007 Mar;18(2):125-9. doi: 10.1097/MBC.0b013e328011c06d. Blood Coagul Fibrinolysis. 2007. PMID: 17287628

6

A heparin cofactor II mutation (HCII Rimini) combined with factor V Leiden or type I protein C deficiency in two unrelated thrombophilic subjects.

Bernardi F, Legnani C, Micheletti F, Lunghi B, Ferraresi P, Palareti G, Biagi R, Marchetti G. Bernardi F, et al. Among authors: ferraresi p. Thromb Haemost. 1996 Oct;76(4):505-9. Thromb Haemost. 1996. PMID: 8902986

7

The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery disease.

Ferraresi P, Marchetti G, Legnani C, Cavallari E, Castoldi E, Mascoli F, Ardissino D, Palareti G, Bernardi F. Ferraresi P, et al. Arterioscler Thromb Vasc Biol. 1997 Nov;17(11):2418-22. doi: 10.1161/01.atv.17.11.2418. Arterioscler Thromb Vasc Biol. 1997. PMID: 9409210

8

Mutations in the R2 FV gene affect the ratio between the two FV isoforms in plasma.

Castoldi E, Rosing J, Girelli D, Hoekema L, Lunghi B, Mingozzi F, Ferraresi P, Friso S, Corrocher R, Tans G, Bernardi F. Castoldi E, et al. Among authors: ferraresi p. Thromb Haemost. 2000 Mar;83(3):362-5. Thromb Haemost. 2000. PMID: 10744138

9

Polymorphisms in the factor VII gene and the risk of myocardial infarction in patients with coronary artery disease.

Girelli D, Russo C, Ferraresi P, Olivieri O, Pinotti M, Friso S, Manzato F, Mazzucco A, Bernardi F, Corrocher R. Girelli D, et al. Among authors: ferraresi p. N Engl J Med. 2000 Sep 14;343(11):774-80. doi: 10.1056/NEJM200009143431104. N Engl J Med. 2000. PMID: 10984565 Free article.

10

Intracellular readthrough of nonsense mutations by aminoglycosides in coagulation factor VII.

Pinotti M, Rizzotto L, Pinton P, Ferraresi P, Chuansumrit A, Charoenkwan P, Marchetti G, Rizzuto R, Mariani G, Bernardi F; International Factor VII Deficiency Study Group. Pinotti M, et al. Among authors: ferraresi p. J Thromb Haemost. 2006 Jun;4(6):1308-14. doi: 10.1111/j.1538-7836.2006.01915.x. J Thromb Haemost. 2006. PMID: 16706976 Free article.

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