If you made any changes in Pure these will be visible here soon.

Research Output

Filter
Article
2019

Severe acquired von Willebrand syndrome secondary to systemic lupus erythematosus

Stufano, F., Baronciani, L., Biguzzi, E., Cozzi, G., Colpani, P., Chisini, M. & Peyvandi, F., 2019, In : Haemophilia. 25, 1, p. e30-e32

Research output: Contribution to journalArticle

2018
2016

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

Pagliari, M. T., Baronciani, L., Stufano, F., Garcia-Oya, I., Cozzi, G., Franchi, F. & Peyvandi, F., Nov 1 2016, In : Haemophilia. 22, 6, p. e502-e511

Research output: Contribution to journalArticle

2015
2013
2012
2011

Von Willebrand factor and fibrinolytic parameters during the desmopressin test in patients with Cushing's disease

Giraldi, F. P., Ambrogio, A. G., Fatti, L. M., Rubini, V., Cozzi, G., Scacchi, M., Federici, A. B. & Cavagnini, F., Jan 2011, In : British Journal of Clinical Pharmacology. 71, 1, p. 132-136 5 p.

Research output: Contribution to journalArticle

2009

Type 2A (IIH) von Willebrand disease is due to mutations that affect von Willebrand factor multimerization

Baronciani, L., Federici, A. B., Punzo, M., Solimando, M., Cozzi, G., La Marca, S., Rubini, V., Canciani, M. T. & Mannucci, P. M., 2009, In : Journal of Thrombosis and Haemostasis. 7, 7, p. 1114-1122 9 p.

Research output: Contribution to journalArticle

2008

Expression studies of missense mutations p.D141Y, p.C275S located in the propeptide of von Willebrand factor in patients with type 3 von Willebrand disease

Baronciani, L., Federici, A. B., Cozzi, G., La Marca, S., Punzo, M., Rubini, V., Canciani, M. T. & Mannucci, P. M., May 2008, In : Haemophilia. 14, 3, p. 549-555 7 p.

Research output: Contribution to journalArticle

2007
2006

von Willebrand factor collagen binding assay in von Willebrand disease type 2A, 2B, and 2M [8]

Baronciani, L., Federici, A. B., Cozzi, G., Canciani, M. T. & Mannucci, P. M., Sep 2006, In : Journal of Thrombosis and Haemostasis. 4, 9, p. 2088-2090 3 p.

Research output: Contribution to journalArticle

2005

Expression studies on a novel type 2B variant of the von Willebrand factor gene (R1308L) characterized by defective collagen binding

Baronciani, L., Federici, A. B., Beretta, M., Cozzi, G., Canciani, M. T. & Mannucci, P. M., Dec 2005, In : Journal of Thrombosis and Haemostasis. 3, 12, p. 2689-2694 6 p.

Research output: Contribution to journalArticle

2003

Molecular defects in type 3 von Willebrand disease: Updated results from 40 multiethnic patients

Baronciani, L., Cozzi, G., Canciani, M. T., Peyvandi, F., Srivastava, A., Federici, A. B. & Mannucci, P. M., May 2003, In : Blood cells, molecules & diseases. 30, 3, p. 264-270 7 p.

Research output: Contribution to journalArticle

2000

Molecular characterization of a multiethnic group of 21 patients with type 3 von Willebrand disease

Baronciani, L., Cozzi, G., Canciani, M. T., Peyvandi, F., Srivastava, A., Federici, A. B. & Mannucci, P. M., 2000, In : Thrombosis and Haemostasis. 84, 4, p. 536-540 5 p.

Research output: Contribution to journalArticle