FAIONI, ELENA MARIA

FAIONI, ELENA MARIA  

Dipartimento di Scienze della Salute  

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Risultati 1 - 20 di 79 (tempo di esecuzione: 0.019 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
A 23bp insertion in the endothelial protein C receptor (EPCR) gene impairs EPCR function 1-gen-2001 E. Faioni + Article (author) -
A factor V genetic component differing from factor V R506Q contributes to the activated protein C resistance phenotype 1-gen-1997 E. Faioni + Article (author) -
A novel G-to-A mutation in intron-N of the protein S gene leading to abnormal RNA splicing in a patient with protein S deficiency 1-gen-2003 E. Faioni + Article (author) -
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 1-apr-2003 E.M. Faioni + Article (author) -
A proteomic analysis of changes in prothrombin and plasma proteins associated with the G20210A mutation 1-lug-2004 C. GelfiE.M. Faioni + Article (author) -
Abnormalities of homocysteine and B vitamins in the nephrotic syndrome 1-gen-2007 G.M. PoddaF. LussanaMORONI, GIOVANNIE.M. FaioniG. FontanaC. MaioliM. Cattaneo + Article (author) -
Activation of protein C in human trophoblasts in culture and downregulation of trophoblast endothelial protein C receptor by TNF-α 1-ago-2015 E.M. FaioniC. RazzariL. AvaglianoG. BulfamanteA.M. Marconi + Article (author) -
ACTIVATION OF THE COAGULATION CASCADE AFTER INFUSION OF A FACTOR-XI CONCENTRATE IN CONGENITALLY DEFICIENT PATIENTS 1-gen-1994 E. FAIONI + Article (author) -
Activation of the protein C pathway in hereditary thrombophilia 1-gen-1998 E. FaioniF. Franchi + Article (author) -
ANOTHER PROTEIN-S FUNCTIONAL ASSAY IS SENSITIVE TO RESISTANCE TO ACTIVATED PROTEIN-C 1-gen-1994 E. FAIONIF. FRANCHI + Article (author) -
Association of estrogen receptor-alpha gene polymorphisms with venous thrombosis 1-gen-2006 F. LussanaE.M. FaioniM. Cattaneo + Article (author) -
Association of factor V deficiency with factor V HR2 1-gen-2004 E.M. FaioniF. Lussana + Article (author) -
Association of protein S p.Pro667Pro dimorphism with plasma protein S levels in normal individuals and patients with inherited protein S deficiency 1-gen-2007 C. RazzariG. FontanaE.M. Faioni + Article (author) -
Atrial fibrillation and psychological factors : a systematic review 11-ago-2017 F. GalliL. BorghiS. CarugoE.M. FaioniE. Vegni + Article (author) -
Autoimmune protein S deficiency and deep vein thrombosis after chickenpox 1-gen-1996 F. PeyvandiE. Faioni + Article (author) -
Bleeding diathesis and gastro-duodenal ulcers in inherited cytosolic phospholipase-A2 alpha deficiency 1-dic-2014 E.M. FaioniC. RazzariE.A. FemiaG. M. PoddaM. PuglianoM. CattaneoA. Zulueta + Article (author) -
c.301C > T (p.Arg101Cys): a novel mutation in the thrombin-sensitive region of protein S associated with a dysfunctional protein 1-gen-2006 E.M. FAIONIP.M. MANNUCCI + Article (author) -
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) 1-gen-1999 E. FaioniF. Franchi + Article (author) -
Complement proteins C5b-9 cause release of membrane vesicles from the platelet surface that are enriched in the membrane receptor for coagulation factor Va and express prothrombinase activity. 1-dic-1988 E.M. Faioni + Article (author) -
Consumption of C4b-binding protein (C4BP) during in vivo activation of the classical complement pathway 1-gen-1999 L. BergamaschiniM. CicardiE. N. FaioniA. Agostoni + Article (author) -