F. Franchi

E. Rondonotti, R. Franchis, S. Saibeni, 2003, Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver.

Increased production of platelet thromboxane B2 in non‐insulin‐dependent diabetes. Relationship to vascular complications

P. Mannucci, G. Pozza, P. Micossi, 1984, European journal of clinical investigation.

Evaluation of an heterogeneous group of patients with von Willebrand disease using an assay alternative to ristocetin induced platelet agglutination

P. Bucciarelli, F. Peyvandi, L. Baronciani, 2015, Journal of thrombosis and haemostasis : JTH.

Monday, 27 August 2012

V. V. Ivanenko, E. A. Medvedeva, Michail I. Papafaklis, 2012 .

CORRECTION OF ABNORMAL COAGULATION IN CHRONIC LIVER DISEASE BY COMBINED USE OF FRESH-FROZEN PLASMA AND PROTHROMBIN COMPLEX CONCENTRATES

P. Mannucci, N. Dioguardi, F. Franchi, 1976, The Lancet.

Coinheritance of the HR 2 Haplotype in the Factor V Gene Confers an Increased Risk of Venous Thromboembolism to Carriers of Factor V R 506 Q ( Factor V Leiden )

M. Margaglione, P. Mannucci, P. Bucciarelli, 1999 .

Primary Malignant Neoplasms Associated with Chronic Lymphocytic Leukemia

A. Santoro, F. Rilke, S. Monfardini, 1980, Tumori.

Activation of the Protein C Pathway in Hereditary Thrombophilia

P. Mannucci, P. Mannucci, E. Faioni, 1998, Thrombosis and Haemostasis.

Clinical staging and therapeutic results in multiple myeloma.

A. Santoro, S. Monfardini, P. Valagussa, 1983, European journal of cancer & clinical oncology.

Endothelial protein C receptor plasma levels increase in chronic liver disease, while thrombomodulin plasma levels increase only in hepatocellular carcinoma.

P. Bucciarelli, M. Colombo, R. Romeo, 2007, Thrombosis research.

Abstract

C. Rabascio, L. Saronni, F. Franchi, 2007 .

Salvage therapy with high dose Intravenous Immunoglobulins in acquired Von Willebrand Syndrome and unresponsive severe intestinal bleeding

F. Peyvandi, M. Cugno, A. Tedeschi, 2014, Experimental Hematology & Oncology.

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

G. Pardi, I. Cetin, E. Faioni, 2001, British journal of haematology.

Coagulation testing before epidural analgesia at delivery: cost analysis.

P. Bucciarelli, F. Rossi, M. Maspero, 2011, Thrombosis research.

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).

M. Margaglione, P. Mannucci, V. De Stefano, 1999, Blood.

Plasma levels of activated protein C in healthy subjects and patients with previous venous thromboembolism: relationships with plasma homocysteine levels.

P. Mannucci, I. Martinelli, M. Cattaneo, 1998, Arteriosclerosis, thrombosis, and vascular biology.

Familial dysfunctional protein C.

P. Mannucci, A. Tripodi, F. Franchi, 1986, Thrombosis research.

Circulating endothelial cells (CECs) and progenitors (CEPs) in severe haemophiliacs with different clinical phenotype

P. Mannucci, E. Santagostino, F. Bertolini, 2009, British journal of haematology.

Alimentary Tract V al34Leu factor XIII polymorphism in Italian patients with inflammatory bowel disease

E. Rondonotti, S. Saibeni, M. Vecchi, 2003 .

Annexin V C/T-1 polymorphism and pregnancy complications.

I. Cetin, I. Martinelli, P. Bucciarelli, 2006, Haematologica.

Clinical Classification and Survival in Chronic Lymphocytic Leukemia

A. Santoro, F. Rilke, S. Monfardini, 1979, Tumori.

Another Protein S Functional Assay Is Sensitive to Resistance to Activated Protein C

P. Mannucci, E. Faioni, M. Wolf, 1994, Thrombosis and Haemostasis.

Budd-Chiari Syndrome in a Patient Heterozygous for the G20210A Mutation of the Prothrombin Gene

M. Moia, P. Bucciarelli, A. Alatri, 1998, Thrombosis and Haemostasis.

Coagulation activation and long-term outcome in acute coronary syndromes Running title: Coagulation activation and long-term outcome in CHD Section heading: Clinical observation

D. Ardissino, P. Mannucci, M. Galvani, 2003 .

Coagulation activation and long-term outcome in acute coronary syndromes.

D. Ardissino, P. Mannucci, M. Galvani, 2003, Blood.

von Willebrand disease type 1 mutation p.Arg1379Cys and the variant p.Ala1377Val synergistically determine a 2M phenotype in four Italian patients

F. Peyvandi, L. Baronciani, M. T. Pagliari, 2016, Haemophilia : the official journal of the World Federation of Hemophilia.

Low borderline plasma levels of antithrombin, protein C and protein S are risk factors for venous thromboembolism

P. Mannucci, I. Martinelli, P. Bucciarelli, 2012, Journal of thrombosis and haemostasis : JTH.

Genetic background and risk of postpartum haemorrhage: results from an Italian cohort of 3219 women

F. Peyvandi, R. Asselta, E. Paraboschi, 2014, Haemophilia : the official journal of the World Federation of Hemophilia.

Protein S binding to phospholipids: evaluation of eight variants of recombinant human protein S from the PROSIT study

C. Razzari, F. Franchi, E. Biguzzi, 2006, Journal of thrombosis and haemostasis : JTH.

Risk factors for postpartum hemorrhage in a cohort of 6011 Italian women.

P. Mannucci, F. Ambrogi, E. Biganzoli, 2012, Thrombosis research.

Marburg I polymorphism of factor VII-activating protease and risk of venous thromboembolism.

P. Mannucci, I. Martinelli, P. Bucciarelli, 2006, Blood.

Low Levels of the Anticoagulant Activity of Protein C in Patients with Chronic Renal Insufficiency: an Inhibitor of Protein C Is Present in Uremic Plasma

G. Remuzzi, P. Mannucci, E. Faioni, 1991, Thrombosis and Haemostasis.

Content and release of beta-thromboglobulin and platelet factor 4 in patients with qualitative platelet defects.

P. Mannucci, D. Pepper, J. Dawes, 1979, Thrombosis Research.

Intrauterine growth restriction and genetic predisposition to thrombophilia.

I. Cetin, P. Bucciarelli, T. Todros, 2004, Haematologica.

A two-step approach (Enzyme-linked immunosorbent assay and confirmation assay) to detect antibodies against von Willebrand factor in patients with Acquired von Willebrand Syndrome.

F. Peyvandi, L. Baronciani, F. Stufano, 2014, Thrombosis research.

Normal reference ranges of antithrombin, protein C and protein S: effect of sex, age and hormonal status.

I. Martinelli, P. Bucciarelli, F. Peyvandi, 2013, Thrombosis research.

Resistance to activated protein C mimicking dysfunctional protein C: diagnostic approach

P. Mannucci, E. Faioni, F. Franchi, 1996, Blood Coagulation and Fibrinolysis.

Asymptomatic homozygous protein C deficiency.

P. Mannucci, A. Tripodi, F. Franchi, 1990, Acta Haematologica.

Functional Assays of Protein C: Comparison of Two Snake-Venom Assays with Two Thrombin Assays

P. Mannucci, A. Tripodi, C. Valsecchi, 1988, Thrombosis and Haemostasis.

The JAK2 V617F mutation in patients with cerebral venous thrombosis

P. Bucciarelli, S. Passamonti, D. Pietra, 2012, Journal of thrombosis and haemostasis : JTH.