Pinotti M - Search Results

1

Coinheritance of Factor V (FV) Leiden enhances thrombin formation and is associated with a mild bleeding phenotype in patients homozygous for the FVII 9726+5G>A (FVII Lazio) mutation.

Castoldi E, Govers-Riemslag JW, Pinotti M, Bindini D, Tans G, Berrettini M, Mazzucconi MG, Bernardi F, Rosing J. Castoldi E, et al. Among authors: pinotti m. Blood. 2003 Dec 1;102(12):4014-20. doi: 10.1182/blood-2003-04-1199. Epub 2003 Jul 24. Blood. 2003. PMID: 12881304 Free article.

2

Molecular bases of CRM+ factor X deficiency: a frequent mutation (Ser334Pro) in the catalytic domain and a substitution (Glu102Lys) in the second EGF-like domain.

Marchetti G, Castaman G, Pinotti M, Lunghi B, Di Iasio MG, Ruggieri M, Rodeghiero F, Bernardi F. Marchetti G, et al. Among authors: pinotti m. Br J Haematol. 1995 Aug;90(4):910-5. doi: 10.1111/j.1365-2141.1995.tb05214.x. Br J Haematol. 1995. PMID: 7669671

3

Molecular defects in CRM+ factor VII deficiencies: modelling of missense mutations in the catalytic domain of FVII.

Bernardi F, Liney DL, Patracchini P, Gemmati D, Legnani C, Arcieri P, Pinotti M, Redaelli R, Ballerini G, Pemberton S, et al. Bernardi F, et al. Among authors: pinotti m. Br J Haematol. 1994 Mar;86(3):610-8. doi: 10.1111/j.1365-2141.1994.tb04793.x. Br J Haematol. 1994. PMID: 8043443

4

Detection of new polymorphic markers in the factor V gene: association with factor V levels in plasma.

Lunghi B, Iacoviello L, Gemmati D, Dilasio MG, Castoldi E, Pinotti M, Castaman G, Redaelli R, Mariani G, Marchetti G, Bernardi F. Lunghi B, et al. Among authors: pinotti m. Thromb Haemost. 1996 Jan;75(1):45-8. Thromb Haemost. 1996. PMID: 8713778

5

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: pinotti m. 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

6

Contribution of factor VII genotype to activated FVII levels. Differences in genotype frequencies between northern and southern European populations.

Bernardi F, Arcieri P, Bertina RM, Chiarotti F, Corral J, Pinotti M, Prydz H, Samama M, Sandset PM, Strom R, Garcia VV, Mariani G. Bernardi F, et al. Among authors: pinotti m. Arterioscler Thromb Vasc Biol. 1997 Nov;17(11):2548-53. doi: 10.1161/01.atv.17.11.2548. Arterioscler Thromb Vasc Biol. 1997. PMID: 9409226

7

Molecular mechanisms of FVII deficiency: expression of mutations clustered in the IVS7 donor splice site of factor VII gene.

Pinotti M, Toso R, Redaelli R, Berrettini M, Marchetti G, Bernardi F. Pinotti M, et al. Blood. 1998 Sep 1;92(5):1646-51. Blood. 1998. PMID: 9716592 Free article.

8

Molecular and clinical aspects of factor VII deficiency.

Mariani G, Lo Coco L, Bernardi F, Pinotti M. Mariani G, et al. Among authors: pinotti m. Blood Coagul Fibrinolysis. 1998 Mar;9 Suppl 1:S83-8. Blood Coagul Fibrinolysis. 1998. PMID: 9819034

9

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. Blood. 2000 Jun 1;95(11):3423-8. Blood. 2000. PMID: 10828024 Free article.

10

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: pinotti m. N Engl J Med. 2000 Sep 14;343(11):774-80. doi: 10.1056/NEJM200009143431104. N Engl J Med. 2000. PMID: 10984565 Free article.

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