List of works - Elena Faioni

Abnormalities of homocysteine and B vitamins in the nephrotic syndrome

scientific article published on 05 February 2007

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

scientific article published on 8 February 2015

Atrial fibrillation and psychological factors: a systematic review.

scientific article published on 11 August 2017

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

scientific article published on 07 August 2014

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

scientific article published on 01 May 1999

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

scientific article published on 25 December 2008

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

scientific article

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

scientific article published on 01 April 2003

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

scientific article published on 23 April 2015

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

scientific article (publication date: 2012)

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

scientific article published in March 2005

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

scientific article

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

scientific article

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

article

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

scientific article published on 25 May 2012

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

scientific article

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

scientific article published on January 2003

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

scientific article published on 11 August 2009

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

scientific article

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

scientific article published on 15 December 2011

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

scientific article published in February 2000

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

scientific article published on January 1, 2003

Why does ticagrelor induce dyspnea?

scientific article published on 16 October 2012

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

scientific article published on 01 September 2006

List of works by Elena Faioni

Abnormalities of homocysteine and B vitamins in the nephrotic syndrome

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

Atrial fibrillation and psychological factors: a systematic review.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Why does ticagrelor induce dyspnea?

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