Luni S - Search Results

1

A protein S functional assay yields unsatisfactory results in patients with activated protein C resistance.

Simioni P, Gavasso S, Luni S, Invidiato S, Girolami A. Simioni P, et al. Among authors: luni s. Blood Coagul Fibrinolysis. 1995 May;6(3):286-7. doi: 10.1097/00001721-199505000-00014. Blood Coagul Fibrinolysis. 1995. PMID: 7654942 No abstract available.

2

Isolation and characterization of an antifactor V antibody causing activated protein C resistance from a patient with severe thrombotic manifestations.

Kalafatis M, Simioni P, Tormene D, Beck DO, Luni S, Girolami A. Kalafatis M, et al. Among authors: luni s. Blood. 2002 Jun 1;99(11):3985-92. doi: 10.1182/blood.v99.11.3985. Blood. 2002. PMID: 12010798 Free article.

3

Compound heterozygous protein C deficiency resulting in the presence of only the beta-form of protein C in plasma.

Simioni P, Kalafatis M, Millar DS, Henderson SC, Luni S, Cooper DN, Girolami A. Simioni P, et al. Among authors: luni s. Blood. 1996 Sep 15;88(6):2101-8. Blood. 1996. PMID: 8822929 Free article.

4

Clinical and laboratory expression of associated thrombophilic conditions (homozygous/heterozygous factor V Leiden mutation and heterozygous prothrombin variant 20210A) in an Italian family.

Simioni P, Tormene D, Luni S, Caldato M, Girolami A. Simioni P, et al. Among authors: luni s. Blood Coagul Fibrinolysis. 2000 Jun;11(4):379-84. doi: 10.1097/00001721-200006000-00010. Blood Coagul Fibrinolysis. 2000. PMID: 10847426

5

The risk of fetal loss in family members of probands with factor V Leiden mutation.

Tormene D, Simioni P, Prandoni P, Luni S, Innella B, Sabbion P, Girolami A. Tormene D, et al. Among authors: luni s. Thromb Haemost. 1999 Oct;82(4):1237-9. Thromb Haemost. 1999. PMID: 10544905

6

Effect of delivery modalities on the physiologic inhibition system of coagulation of the neonate.

Franzoi M, Simioni P, Luni S, Zerbinati P, Girolami A, Zanardo V. Franzoi M, et al. Among authors: luni s. Thromb Res. 2002 Jan 1;105(1):15-8. doi: 10.1016/s0049-3848(01)00407-8. Thromb Res. 2002. PMID: 11864701

7

Abnormal propeptide processing resulting in the presence of two abnormal species of protein C in plasma: characterization of the dysfunctional protein C Padua3 (protein C(R-1L/propeptide)).

Simioni P, Kalafatis M, Tormene D, Luni S, Zerbinati P, Barzon L, Palù G, Girolami A. Simioni P, et al. Among authors: luni s. Thromb Haemost. 2001 Oct;86(4):1017-22. Thromb Haemost. 2001. PMID: 11686318

8

Prothrombin antigen levels in symptomatic and asymptomatic carriers of the 20210A prothrombin variant.

Simioni P, Tormene D, Manfrin D, Gavasso S, Luni S, Stocco D, Girolami A. Simioni P, et al. Among authors: luni s. Br J Haematol. 1998 Dec;103(4):1045-50. doi: 10.1046/j.1365-2141.1998.01112.x. Br J Haematol. 1998. PMID: 9886317 Free article.

9

A new factor X defect (factor X Padua 3): a compound heterozygous between true deficiency (Gly(380)-->Arg) and an abnormality (Ser(334)-->Pro).

Vianello F, Lombardi AM, Boldrin C, Luni S, Girolami A. Vianello F, et al. Among authors: luni s. Thromb Res. 2001 Nov 15;104(4):257-64. doi: 10.1016/s0049-3848(01)00371-1. Thromb Res. 2001. PMID: 11728527

10

Asymptomatic homozygous nt 20210 G to A prothrombin polymorphism in two blood donors belonging to two different kindreds.

Girolami A, Simioni P, Manfrin D, Tormene D, Luni S. Girolami A, et al. Among authors: luni s. Clin Appl Thromb Hemost. 1999 Jan;5(1):48-51. doi: 10.1177/107602969900500110. Clin Appl Thromb Hemost. 1999. PMID: 10725983 Free article.

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