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Items: 1 to 50 of 66

1.

Failure of the Anticoagulant Therapy and Psychological Distress: Still Far From a Bridge.

Galli F, Borghi L, Faioni E, Cavicchioli M, Ferrari Losi J, Vegni E.

Front Psychol. 2018 Sep 13;9:1709. doi: 10.3389/fpsyg.2018.01709. eCollection 2018.

2.

Sex, gender and venous thromboembolism: do we care enough?

Faioni EM, Zighetti ML, Vozzo NP.

Blood Coagul Fibrinolysis. 2018 Dec;29(8):663-667. doi: 10.1097/MBC.0000000000000773. Review.

PMID:
30234546
3.

Atrial fibrillation and psychological factors: a systematic review.

Galli F, Borghi L, Carugo S, Cavicchioli M, Faioni EM, Negroni MS, Vegni E.

PeerJ. 2017 Aug 11;5:e3537. doi: 10.7717/peerj.3537. eCollection 2017.

4.

Soluble endothelial protein C receptor (sEPCR) as an inflammatory biomarker in naive HIV-infected patients during ART.

Chiappetta S, Ripa M, Galli L, Razzari C, Longo V, Galli A, Faioni EM, Nozza S, Lazzarin A, Tambussi G.

J Antimicrob Chemother. 2016 Jun;71(6):1627-31. doi: 10.1093/jac/dkw010. Epub 2016 Feb 16.

PMID:
26888911
5.

Instability of cytosolic phospholipase A2α variant upon cellular expression as a basis for its clinical presentation.

Zulueta A, Razzari C, Fontana G, Femia EA, Faioni EM, Cattaneo M, Trinchera M.

Thromb Haemost. 2015 Jul;114(1):208-10. doi: 10.1160/TH14-11-0926. Epub 2015 Apr 23. No abstract available.

PMID:
25904158
6.

Activation of Protein C in Human Trophoblasts in Culture and Downregulation of Trophoblast Endothelial Protein C Receptor by TNF-α.

Faioni EM, Fontana G, Razzari C, Avagliano L, Bulfamante G, Calvi E, Doi P, Marconi AM.

Reprod Sci. 2015 Aug;22(8):1042-8. doi: 10.1177/1933719115570904. Epub 2015 Feb 8.

PMID:
25667200
7.

Naturally occurring N(6)-substituted adenosines (cytokinin ribosides) are in vitro inhibitors of platelet aggregation: an in silico evaluation of their interaction with the P2Y(12) receptor.

Vistoli G, Brizzolari A, Faioni E, Razzari C, Santaniello E.

Bioorg Med Chem Lett. 2014 Dec 15;24(24):5652-5655. doi: 10.1016/j.bmcl.2014.10.080. Epub 2014 Oct 30.

PMID:
25467153
8.

Bleeding diathesis and gastro-duodenal ulcers in inherited cytosolic phospholipase-A2 alpha deficiency.

Faioni EM, Razzari C, Zulueta A, Femia EA, Fenu L, Trinchera M, Podda GM, Pugliano M, Marongiu F, Cattaneo M.

Thromb Haemost. 2014 Dec;112(6):1182-9. doi: 10.1160/TH14-04-0352. Epub 2014 Aug 7.

PMID:
25102815
9.

Why does ticagrelor induce dyspnea?

Cattaneo M, Faioni EM.

Thromb Haemost. 2012 Dec;108(6):1031-6. doi: 10.1160/TH12-08-0547. Epub 2012 Oct 16. Review.

PMID:
23070079
10.

Levels of soluble endothelial protein C receptor are associated with CD4+ changes in Maraviroc-treated HIV-infected patients.

Nozza S, Pogliaghi M, Chiappetta S, Spagnuolo V, Fontana G, Razzari C, Tambussi G, Faioni EM.

PLoS One. 2012;7(6):e37032. doi: 10.1371/journal.pone.0037032. Epub 2012 Jun 8.

11.

Prevalence of factor V Leiden and G20210A prothrombin mutation in the Dutch Famine Birth Cohort: a possible survival advantage?

Lussana F, de Rooij SR, Veenendaal M, Razzari C, Fontana G, Faioni EM, Painter RC, Middeldorp S, Cattaneo M, Roseboom TJ.

Thromb Haemost. 2012 Aug;108(2):399-401. doi: 10.1160/TH12-03-0145. Epub 2012 May 25. No abstract available.

PMID:
22627863
12.

To be or not to be: the patient's view of thrombophilia testing.

Vegni E, Leone D, Graffigna G, Faioni EM, Moja EA.

Patient Educ Couns. 2013 Mar;90(3):386-91. doi: 10.1016/j.pec.2011.11.002. Epub 2011 Dec 15.

PMID:
22177659
13.

Screening for thrombophilia and antithrombotic prophylaxis in pregnancy: Guidelines of the Italian Society for Haemostasis and Thrombosis (SISET).

Lussana F, Dentali F, Abbate R, d'Aloja E, D'Angelo A, De Stefano V, Faioni EM, Grandone E, Legnani C, Martinelli I, Simioni P, Tormene D; Italian Society for Haemostasis and Thrombosis.

Thromb Res. 2009 Nov;124(5):e19-25. doi: 10.1016/j.thromres.2009.06.031. Epub 2009 Aug 11.

PMID:
19671474
14.

Determination of vitamin K1 in plasma by solid phase extraction and HPLC with fluorescence detection.

Paroni R, Faioni EM, Razzari C, Fontana G, Cattaneo M.

J Chromatogr B Analyt Technol Biomed Life Sci. 2009 Jan 15;877(3):351-4. doi: 10.1016/j.jchromb.2008.12.044. Epub 2008 Dec 25.

PMID:
19129011
15.

ProCMD: a database and 3D web resource for protein C mutants.

D'Ursi P, Marino F, Caprera A, Milanesi L, Faioni EM, Rovida E.

BMC Bioinformatics. 2007 Mar 8;8 Suppl 1:S11.

16.

Abnormalities of homocysteine and B vitamins in the nephrotic syndrome.

Podda GM, Lussana F, Moroni G, Faioni EM, Lombardi R, Fontana G, Ponticelli C, Maioli C, Cattaneo M.

Thromb Res. 2007;120(5):647-52. Epub 2007 Feb 5.

PMID:
17276499
17.

Association of protein S p.Pro667Pro dimorphism with plasma protein S levels in normal individuals and patients with inherited protein S deficiency.

Castaman G, Biguzzi E, Razzari C, Tosetto A, Fontana G, Asti D, Brancaccio V, Castori D, Lane DA, Faioni EM; ProSIT (Protein S Italian Team).

Thromb Res. 2007;120(3):421-6. Epub 2006 Dec 15.

PMID:
17157360
18.

Identification and computationally-based structural interpretation of naturally occurring variants of human protein C.

Rovida E, Merati G, D'Ursi P, Zanardelli S, Marino F, Fontana G, Castaman G, Faioni EM.

Hum Mutat. 2007 Apr;28(4):345-55.

PMID:
17152060
19.

c.301C > T (p.Arg101Cys): a novel mutation in the thrombin-sensitive region of protein S associated with a dysfunctional protein.

Franchi F, Viscardi Y, Razzari C, Faioni EM, Bonara P, Biguzzi E, Mannucci PM.

Thromb Haemost. 2006 Sep;96(3):381-3. No abstract available.

PMID:
16953283
20.

Association of estrogen receptor-alpha genepolymorphisms with venous thrombosis.

Lussana F, Faioni EM, Mavilia C, Bucciarelli P, Brandi ML, Cattaneo M.

Haematologica. 2006 Feb;91(2):279-80.

21.

Molecular diversity and thrombotic risk in protein S deficiency: the PROSIT study.

Biguzzi E, Razzari C, Lane DA, Castaman G, Cappellari A, Bucciarelli P, Fontana G, Margaglione M, D'Andrea G, Simmonds RE, Rezende SM, Preston R, Prisco D, Faioni EM; Protein S Italian Team.

Hum Mutat. 2005 Mar;25(3):259-69.

PMID:
15712227
22.

A proteomic analysis of changes in prothrombin and plasma proteins associated with the G20210A mutation.

Gelfi C, Viganò A, Ripamonti M, Wait R, Begum S, Biguzzi E, Castaman G, Faioni EM.

Proteomics. 2004 Jul;4(7):2151-9.

PMID:
15221775
23.

Expression of endothelial protein C receptor and thrombomodulin in the intestinal tissue of patients with inflammatory bowel disease.

Faioni EM, Ferrero S, Fontana G, Gianelli U, Ciulla MM, Vecchi M, Saibeni S, Biguzzi E, Cordani N, Franchi F, Bosari S, Cattaneo M.

Crit Care Med. 2004 May;32(5 Suppl):S266-70.

PMID:
15118529
24.

Expression of endothelial protein C receptor and thrombomodulin in human coronary atherosclerotic plaques.

Merlini PA, Rossi ML, Faioni EM, Franchi F, Bramucci E, Lucreziotti S, Biguzzi E, Mannucci PM, Ardissino D.

Ital Heart J. 2004 Jan;5(1):42-7.

PMID:
15080580
25.

Review of clinical, biochemical and genetic aspects of combined factor V and factor VIII deficiency, and report of a new affected family.

Faioni EM, Fontana G, Carpani G, D'Auria E, Banderali G, Moroni G, Cattaneo M.

Thromb Res. 2003;112(5-6):269-71. Review. No abstract available.

PMID:
15041268
26.

Association of factor V deficiency with factor V HR2.

Faioni EM, Castaman G, Asti D, Lussana F, Rodeghiero F.

Haematologica. 2004 Feb;89(2):195-200.

27.

The factor V HR2 haplotype and the risk of venous thrombosis: a meta-analysis.

Castaman G, Faioni EM, Tosetto A, Bernardi F.

Haematologica. 2003 Oct;88(10):1182-9.

28.

Identification of differentially expressed genes in coronary atherosclerotic plaques from patients with stable or unstable angina by cDNA array analysis.

Randi AM, Biguzzi E, Falciani F, Merlini P, Blakemore S, Bramucci E, Lucreziotti S, Lennon M, Faioni EM, Ardissino D, Mannucci PM.

J Thromb Haemost. 2003 Apr;1(4):829-35.

29.

Val34Leu factor XIII polymorphism in Italian patients with inflammatory bowel disease.

Saibeni S, Vecchi M, Faioni EM, Franchi F, Rondonotti E, Borsi G, de Franchis R.

Dig Liver Dis. 2003 Jan;35(1):32-6.

PMID:
12725605
30.

A novel G-to-A mutation in the intron-N of the protein S gene leading to abnormal RNA splicing in a patient with protein S deficiency.

D'Andrea G, Di Perna P, Brancaccio V, Faioni EM, Castaman G, Cibelli G, Di Minno G, Margaglione M; Protein S Italian Team.

Haematologica. 2003 Apr;88(4):459-64.

31.

No effect of fasting plasma total homocysteine on protein C activity in vitro.

Podda G, Faioni EM, Zighetti ML, Cattaneo M.

Blood. 2003 Mar 15;101(6):2446-7. No abstract available.

PMID:
12609965
32.

Mutations in the thrombomodulin gene are rare in patients with severe thrombophilia.

Faioni EM, Franchi F, Castaman G, Biguzzi E, Rodeghiero F.

Br J Haematol. 2002 Aug;118(2):595-9.

PMID:
12139752
33.

Reliable estimates of plasma protein S levels: are we getting any closer?

Faioni EM.

Thromb Haemost. 2001 Nov;86(5):1139-40. No abstract available.

PMID:
11816696
34.

A 23bp insertion in the endothelial protein C receptor (EPCR) gene impairs EPCR function.

Biguzzi E, Merati G, Liaw PC, Bucciarelli P, Oganesyan N, Qu D, Gu JM, Fetiveau R, Esmon CT, Mannucci PM, Faioni EM.

Thromb Haemost. 2001 Oct;86(4):945-8.

PMID:
11686350
35.

Mutations in the thrombomodulin and endothelial protein C receptor genes in women with late fetal loss.

Franchi F, Biguzzi E, Cetin I, Facchetti F, Radaelli T, Bozzo M, Pardi G, Faioni EM.

Br J Haematol. 2001 Sep;114(3):641-6.

PMID:
11552992
36.

Reduced free protein S levels in patients with inflammatory bowel disease: prevalence, clinical relevance, and role of anti-protein S antibodies.

Saibeni S, Vecchi M, Valsecchi C, Faioni EM, Razzari C, de Franchis R.

Dig Dis Sci. 2001 Mar;46(3):637-43.

PMID:
11318545
37.

Factor V HR2: an ancient haplotype out of Africa--reasons for being interested.

Faioni EM.

Thromb Haemost. 2000 Mar;83(3):358-9. Review. No abstract available.

PMID:
10744136
38.

Type II protein C deficiency: identification and molecular modelling of two natural mutants with low anticoagulant and normal amidolytic activity.

Faioni EM, Hermida J, Rovida E, Razzari C, Asti D, Zeinali S, Mannucci PM.

Br J Haematol. 2000 Feb;108(2):265-71.

PMID:
10691853
39.

Poor relationship between phenotypes of protein S deficiency and mutations in the protein S alpha gene.

Hermida J, Faioni EM, Mannucci PM.

Thromb Haemost. 1999 Dec;82(6):1634-8.

PMID:
10613647
40.

Coinheritance of the HR2 haplotype in the factor V gene confers an increased risk of venous thromboembolism to carriers of factor V R506Q (factor V Leiden).

Faioni EM, Franchi F, Bucciarelli P, Margaglione M, De Stefano V, Castaman G, Finazzi G, Mannucci PM.

Blood. 1999 Nov 1;94(9):3062-6.

PMID:
10556190
41.

Consumption of C4b-binding protein (C4BP) during in vivo activation of the classical complement pathway.

Bergamaschini L, Miedico A, Cicardi M, Coppola R, Faioni EN, Agostoni A.

Clin Exp Immunol. 1999 May;116(2):220-4.

42.
43.

Activation of the protein C pathway in hereditary thrombophilia.

Faioni EM, Franchi F, Asti D, Mannucci PM.

Thromb Haemost. 1998 Oct;80(4):557-60.

PMID:
9798968
44.

Different risks of thrombosis in four coagulation defects associated with inherited thrombophilia: a study of 150 families.

Martinelli I, Mannucci PM, De Stefano V, Taioli E, Rossi V, Crosti F, Paciaroni K, Leone G, Faioni EM.

Blood. 1998 Oct 1;92(7):2353-8.

PMID:
9746774
45.

Free protein S deficiency is a risk factor for venous thrombosis.

Faioni EM, Valsecchi C, Palla A, Taioli E, Razzari C, Mannucci PM.

Thromb Haemost. 1997 Nov;78(5):1343-6.

PMID:
9408016
46.

A factor V genetic component differing from factor V R506Q contributes to the activated protein C resistance phenotype.

Bernardi F, Faioni EM, Castoldi E, Lunghi B, Castaman G, Sacchi E, Mannucci PM.

Blood. 1997 Aug 15;90(4):1552-7.

PMID:
9269773
47.

Resistance to activated protein C in unselected patients with arterial and venous thrombosis.

Faioni EM, Razzari C, Martinelli I, Panzeri D, Franchi F, Mannucci PM.

Am J Hematol. 1997 Jun;55(2):59-64.

48.

Venocclusive disease of the liver after bone marrow transplantation: the role of hemostasis.

Faioni EM, Mannucci PM.

Leuk Lymphoma. 1997 Apr;25(3-4):233-45. Review.

PMID:
9168434
49.

The G1456 to T mutation in the thrombomodulin gene is not frequent in patients with venous thrombosis.

Faioni EM, Merati G, Peyvandi F, Bettini PM, Mannucci PM.

Blood. 1997 Feb 15;89(4):1467. No abstract available.

50.

Heightened thrombin generation in individuals with resistance to activated protein C.

Martinelli I, Bottasso B, Duca F, Faioni E, Mannucci PM.

Thromb Haemost. 1996 May;75(5):703-5.

PMID:
8725708

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