E. Sacchi

发表

Effect of 4G/5G PAI-1 polymorphism on the response of PAI-1 activity to vitamin E supplementation in Type 2 diabetic patients.

R. Testa, A. Bonfigli, C. Sirolla, 2004, Diabetes, nutrition & metabolism.

Gene polymorphisms predicting high plasma levels of coagulation and fibrinolysis proteins. A study in centenarians.

D. Mari, E. Sacchi, C. Franceschi, 1997, Arteriosclerosis, Thrombosis and Vascular Biology.

High Frequency of the C677T Mutation in the Methylenetetrahydrofolate Reductase (MTHFR) Gene in Northern Italy

E. Sacchi, P. Mannucci, P. Mannucci, 1997, Thrombosis and Haemostasis.

Intravenous and Subcutaneous Administration of Desmopresssin (DDAVP) to Hemophiliacs: Pharmacokinetics and Factor VIII Responses

E. Sacchi, P. Mannucci, G. Longo, 1987, Thrombosis and Haemostasis.

Plasminogen activator inhibitor-1 plasma level increases with age in subjects with the 4G allele at position -675 in the promoter region

A. Bonfigli, C. Sirolla, M. Boemi, 2004, Thrombosis and Haemostasis.

Plasma factor VII levels are influenced by a polymorphism in the promoter region of the FVII gene

E. Sacchi, P. Mannucci, F. Bernardi, 1996, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Inflammatory bowel disease are not associated with the major hereditary conditions predisposing to thrombosis

E. Sacchi, P. Mannucci, R. Franchis, 1998 .

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

E. Sacchi, P. Mannucci, F. Bernardi, 1997, Blood.

Prothrombin Gene Mutation (G20210A) in Healthy Centenarians

D. Mari, E. Sacchi, C. Franceschi, 1999, Thrombosis and Haemostasis.

HELLP syndrome and factor V Leiden.

E. Sacchi, G. Pardi, S. Marcozzi, 2001, European journal of obstetrics, gynecology, and reproductive biology.

Resistance to Activated Protein C in Nine Thrombophilic Families: Interference in a Protein S Functional Assay

E. Sacchi, P. Mannucci, F. Bernardi, 1993, Thrombosis and Haemostasis.

A rapid assay for ristocetin cofactor activity using an automated coagulometer (ACL 9000)

E. Sacchi, A. Federici, E. Rossi, 2004, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Carrier detection and prenatal diagnosis of hemophilia A: 5-years experience at a hemophilia center

E. Sacchi, P. Mannucci, L. Tagliavacca, 1992, International journal of clinical & laboratory research.

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

E. Sacchi, F. Bernardi, P. Mannucci, 1997 .

High risk of cerebral-vein thrombosis in carriers of a prothrombin-gene mutation and in users of oral contraceptives.

E. Sacchi, E. Taioli, P. Mannucci, 1998, The New England journal of medicine.

Inflammatory Bowel Diseases Are Not Associated with Major Hereditary Conditions Predisposing to Thrombosis

E. Sacchi, S. Saibeni, M. Vecchi, 2000, Digestive Diseases and Sciences.

Absence of the Prothrombin Gene Variant in Koreans

D. Mari, E. Sacchi, C. Franceschi, 2012 .

No Evidence of Association Between Prothrombotic Gene Polymorphisms and the Development of Acute Myocardial Infarction at a Young Age

M. Margaglione, A. Piazza, L. Bernardinelli, 2003, Circulation.

Protein S mRNA in Patients with Protein S Deficiency

E. Sacchi, P. Mannucci, M. Pinotti, 1995, Thrombosis and Haemostasis.

Are intravenous immunoglobulins really inappropriate in acquired von Willebrand syndrome?

E. Sacchi, V. Rossi, M. Franchini, 2012, Blood transfusion = Trasfusione del sangue.

C-reactive protein is directly related to plasminogen activator inhibitor type 1 (PAI-1) levels in diabetic subjects with the 4G allele at position -675 of the PAI-1 gene.

R. Testa, A. Bonfigli, C. Sirolla, 2008, Nutrition, metabolism, and cardiovascular diseases : NMCD.

The Genetic Defect of Type I von Willebrand Disease “Vicenza” Is Linked to the von Willebrand Factor Gene

E. Sacchi, P. Mannucci, F. Rodeghiero, 1993, Thrombosis and Haemostasis.

Supportive transfusion therapy in cancer patients with acquired defects of hemostasis.

E. Sacchi, D. Intini, A. Federici, 2014, Thrombosis research.

Carrier detection and feasibility of prenatal diagnosis of hemophilia B by multiplex polymerase chain reaction

E. Sacchi, P. Mannucci, L. Tagliavacca, 1993, International journal of clinical & laboratory research.

Diagnosis of hemophilia a in a female subject by using restriction fragment length polymorphisms linked to the factor VIII gene

E. Sacchi, P. Mannucci, G. Muleo, 1989, La Ricerca in clinica e in laboratorio.

A novel polymorphism in intron 1a of the human factor VII gene (G73A): study of a healthy Italian population and of 190 young survivors of myocardial infarction

Sacchi, E. Sacchi, P. Mannucci, 2000, British journal of haematology.