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Journal Articles

Clustering of Bleeding Symptoms in Patients Previously Diagnosed As Type 3 Von Willebrand Disease: Results from a Large Cohort of Type 3 Von Willebrand Disease (the 3Winters-Ips Project)

Blood (2018) 132 (Supplement 1): 2465.

https://doi.org/10.1182/blood-2018-99-113996

Published: 2018

Journal Articles

Profile of Mutations Identified in the 3WINTERS-IPS Project on European & Iranian Patients with Previously Diagnosed Type 3 Von Willebrand Disease.

Luciano Baronciani, PhD, Flora Peyvandi, MD PhD, Anne Goodeve, PhD, Reinhard Schneppenheim, MDPhD, Zahra Badiee, Mohammad-Reza Baghaipour, Javier Battle, Erik Berntorp, MD PhD, Imre Bodó, MD PhD, Ulrich Budde, MD, Andrea Cairo, PhD, Giancarlo Castaman, Laura Crookes, Jeroen C.J. Eikenboom, MD, Peyman Eshghi, MD, Cosimo Ettorre, MD, Jenny Goudemand, MD PhD, Wolf Hassenpflug, Charles Richard Morris Hay, MDFRCP,FRCPath, Hamid Hoorfar, MD, Mehran Karimi, MD, Bijan Keikhaei, Riitta Lassila, MD PR, Frank W.G. Leebeek, MD PhD, Maria Fernanda Lopez Fernandez, Pier Mannuccio Mannucci, MD, Maria Gabriella Mazzucconi, MD, Massimo Morfini, MD, Nikolas Nikšić, Johannes Oldenburg, Florian Oyen, Rafael Parra Lòpez, Ian Peake, PhD, Gholamreza Toogeh, Alberto Tosetto, Marc Trossaert, Sayed Omid Reza Zekavat, MD, Eva M.K. Zetterberg, MD PhD, Augusto B Federici, MD

Blood (2018) 132 (Supplement 1): 1184.

https://doi.org/10.1182/blood-2018-99-114702

Published: 2018

Journal Articles

The R1306W Type 2B Natural Mutation of Von Willebrand Factor Dramatically Enhances the Multimer Sensitivity to Shear Stress

Raimondo De Cristofaro, Giovanni Luca Scaglione, Stefano Lancellotti, Maria Teresa Pagliari, Massimiliano Papi, Marco De Spirito, Alessandro Maiorana, Luciano Baronciani, Alessandro Arcovito, Enrico Di Stasio, Flora Peyvandi

Blood (2012) 120 (21): 3306.

https://doi.org/10.1182/blood.V120.21.3306.3306

Published: 2012

Journal Articles

A Two-Year Prospective Study on Bleeding Tendency In 105 Patients with Type 2 A and M Von Willebrand Disease

Giancarlo Castaman, MD, Augusto B. Federici, MD, Luciano Baronciani, Pier M. Mannucci, MD, Francesco Rodeghiero

Blood (2010) 116 (21): 543.

https://doi.org/10.1182/blood.V116.21.543.543

Published: 2010

Journal Articles

Abnormal VWF modifies megakaryocytopoiesis: studies of platelets and megakaryocyte cultures from patients with von Willebrand disease type 2B

Paquita Nurden, Giuliana Gobbi, Alan Nurden, Jocelyne Enouf, Ibtissam Youlyouz-Marfak, Cecilia Carubbi, Silvia La Marca, Margherita Punzo, Luciano Baronciani, Luigi De Marco, Marco Vitale, Augusto B. Federici

Blood (2010) 115 (13): 2649–2656.

https://doi.org/10.1182/blood-2009-07-231886

Published: 2010

Journal Articles

The Use of High Resolution Melting (HRM) Analysis for Molecular Gene Defects of Type 3 Von Willebrand Disease: Studies of An Italian Cohort of 10 Patients.

Maria Solimando, Augusto B. Federici, Luciano Baronciani, Alberto Mussetti, Margherita Punzo, Silvia La Marca, Manuela Platè, Rosanna Asselta, Pier Mannuccio Mannucci

Blood (2009) 114 (22): 3498.

https://doi.org/10.1182/blood.V114.22.3498.3498

Published: 2009

Journal Articles

Clinical and molecular predictors of thrombocytopenia and risk of bleeding in patients with von Willebrand disease type 2B: a cohort study of 67 patients

Augusto B. Federici, Pier M. Mannucci, Giancarlo Castaman, Luciano Baronciani, Paolo Bucciarelli, Maria T. Canciani, Alessandro Pecci, Peter J. Lenting, Philip G. De Groot

Blood (2009) 113 (3): 526–534.

https://doi.org/10.1182/blood-2008-04-152280

Published: 2009

Journal Articles

Circulating Versus Progenitor Endothelial Cells Levels Are Abnormal in Patients with Different Types of Von Willebrand Disease and Correlate with Markers of Angiogenesis

Giuseppe Gritti, MD, Augusto B Federici, MD, Agostino Cortelezzi, MD, Luciano Baronciani, PhD, Silvia Lonati, PhD, Margherita Punzo, Ilaria Silvestris, Rosanna Garavaglia, MD, Giorgio Lambertenghi, MD, Pier M Mannucci, MD

Blood (2008) 112 (11): 5457.

https://doi.org/10.1182/blood.V112.11.5457.5457

Published: 2008

Journal Articles

Relevance of Chloride Binding to Von Willebrand Factor in Type 2B Von Willebrand Disease Patients.

Luciano Baronciani, PhD, Flora Peyvandi, MD, Margherita Punzo, PhD, Maria T. Canciani, PhD, Enrico Di Stasio, MD, Augusto B. Federici, MD, Pier M. Mannucci, MD, Raimondo De Cristofaro, MD

Blood (2008) 112 (11): 3384.

https://doi.org/10.1182/blood.V112.11.3384.3384

Published: 2008

Journal Articles

Morphological Changes of Platelets from Patients with Von Willebrand Disease Types 2B and 3 Suggest That Von Willebrand Factor Intervenes in Platelet Formation from Megakaryocytes.

Paquita Nurden, Alan T Nurden, Jean-Max Pasquet, Jocelyne Enouf, Cécile Faurie-Bonnafous, Sylvia La Marca, Margherita Punzo, Luciano Baronciani, Augusto B. Federici

Blood (2008) 112 (11): 1238.

https://doi.org/10.1182/blood.V112.11.1238.1238

Published: 2008

Journal Articles

Type 2B “Malmo/New York” Is Not So Rare among Italian Patients with von Willebrand Disease: The Role of P1266L/Q Mutations of the von Willebrand Factor Gene in Seven Cases.

Luciano Baronciani, PhD, Silvia La Marca, PhD, Giancarlo Castaman, MD, Margherita Punzo, PhD, Rosanna Garavaglia, MD, Valentina Rubini, PhD, Giovanna Cozzi, PhD, Maria T. Canciani, PhD, Augusto B. Federici, MD

Blood (2007) 110 (11): 712.

https://doi.org/10.1182/blood.V110.11.712.712

Published: 2007

Journal Articles

Abnormal Large Platelets Are Associated Not Only with von Willebrand Disease (VWD) Type 2B (Including Type 2B/1 New York) but Also with Severe Type 3: A Potential Role for von Willebrand Factor (VWF) in Megakaryocytopoiesis.

Paquita Nurden, MD, PhD, Alan T. Nurden, PhD, Jocelyne Enouf, PhD, Silvia La Marca, Luciano Baronciani, Augusto B. Federici, MD, PhD

Blood (2007) 110 (11): 101.

https://doi.org/10.1182/blood.V110.11.101.101

Published: 2007

Journal Articles

Studies with the Nanobody That Detects the Gain-of-Function of von Willebrand Factor in a Cohort of Patients with Type 2B von Willebrand Disease: Correlation with Platelet Count, VWF Multimers and Molecular Defects.

Augusto B. Federici, MD, Luciano Baronciani, PhD, Maria T. Canciani, PhD, Barbara Moroni, PhD, Carlo Balduini, MD, Pier M. Mannucci, MD, Peter J. Lenting, PhD, Philip G. de Groot, PhD

Blood (2006) 108 (11): 1011.

https://doi.org/10.1182/blood.V108.11.1011.1011

Published: 2006

Journal Articles

Molecular Mapping of the Chloride Binding Site in von Willebrand Factor (VWF): Energetics and Conformational Effects on the ADAMTS-13 Interaction with Wild Type and Type 2B R1306W VWF Forms.

Raimondo De Cristofaro, MD, Flora Peyvandi, MD, Luciano Baronciani, PhD, Roberta Palla, PhD, Silvia Lavoretano, PhD, Rossana Lombardi, PhD, Enrico Di Stasio, MD, Augusto B. Federici, MD, Pier Mannuccio Mannucci, MD

Blood (2006) 108 (11): 333.

https://doi.org/10.1182/blood.V108.11.333.333

Published: 2006

Journal Articles

Phenotype and genotype of a cohort of families historically diagnosed with type 1 von Willebrand disease in the European study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 von Willebrand Disease (MCMDM-1VWD)

Blood (2006) 109 (1): 112–121.

https://doi.org/10.1182/blood-2006-05-020784

Published: 2006

Includes: Supplemental data

Journal Articles

An Association of Candidate Gene Haplotypes and Bleeding Severity in von Willebrand Disease (VWD) Type 2 Pedigrees.

Thomas J. Kunicki, Luciano Baronciani, Maria Teresa Canciani, Francesca Gianniello, Augusto B. Federici

Blood (2004) 104 (11): 3036.

https://doi.org/10.1182/blood.V104.11.3036.3036

Published: 2004

Journal Articles

Biochemical Characterization of Recombinant Von Willebrand Factor (VWF) with a Type 2B Mutation (P1337L) Coexpressed with a Type 1 VWF Defect (C275R): A Complex Molecular Defect in a Patient Previously Diagnosed with Type 2A Von Willebrand Disease (VWD).

Luciano Baronciani, PhD, Augusto B. Federici, MD, Matteo Beretta, PhD, Giovanna Cozzi, PhD, Maria T. Canciani, PhD, Pier M. Mannucci, MD

Blood (2004) 104 (11): 1025.

https://doi.org/10.1182/blood.V104.11.1025.1025

Published: 2004

Journal Articles

An association of candidate gene haplotypes and bleeding severity in von Willebrand disease (VWD) type 1 pedigrees

Thomas J. Kunicki, Augusto B. Federici, Daniel R. Salomon, James A. Koziol, Steven R. Head, Tony S. Mondala, Jeffrey D. Chismar, Luciano Baronciani, Maria Teresa Canciani, Ian R. Peake

Blood (2004) 104 (8): 2359–2367.

https://doi.org/10.1182/blood-2004-01-0349

Published: 2004

Journal Articles

Molecular Characterization of PK-LR Gene in Pyruvate Kinase–Deficient Italian Patients

Alberto Zanella, Paola Bianchi, Luciano Baronciani, Manuela Zappa, Elena Bredi, Cristina Vercellati, Fiorella Alfinito, Giovanni Pelissero, Girolamo Sirchia

Blood (1997) 89 (10): 3847–3852.

https://doi.org/10.1182/blood.V89.10.3847

Published: 1997

NARROW

Clustering of Bleeding Symptoms in Patients Previously Diagnosed As Type 3 Von Willebrand Disease: Results from a Large Cohort of Type 3 Von Willebrand Disease (the 3Winters-Ips Project)

Profile of Mutations Identified in the 3WINTERS-IPS Project on European & Iranian Patients with Previously Diagnosed Type 3 Von Willebrand Disease.

The R1306W Type 2B Natural Mutation of Von Willebrand Factor Dramatically Enhances the Multimer Sensitivity to Shear Stress

A Two-Year Prospective Study on Bleeding Tendency In 105 Patients with Type 2 A and M Von Willebrand Disease

Abnormal VWF modifies megakaryocytopoiesis: studies of platelets and megakaryocyte cultures from patients with von Willebrand disease type 2B

The Use of High Resolution Melting (HRM) Analysis for Molecular Gene Defects of Type 3 Von Willebrand Disease: Studies of An Italian Cohort of 10 Patients.

Clinical and molecular predictors of thrombocytopenia and risk of bleeding in patients with von Willebrand disease type 2B: a cohort study of 67 patients

Circulating Versus Progenitor Endothelial Cells Levels Are Abnormal in Patients with Different Types of Von Willebrand Disease and Correlate with Markers of Angiogenesis

Relevance of Chloride Binding to Von Willebrand Factor in Type 2B Von Willebrand Disease Patients.

Morphological Changes of Platelets from Patients with Von Willebrand Disease Types 2B and 3 Suggest That Von Willebrand Factor Intervenes in Platelet Formation from Megakaryocytes.

Type 2B “Malmo/New York” Is Not So Rare among Italian Patients with von Willebrand Disease: The Role of P1266L/Q Mutations of the von Willebrand Factor Gene in Seven Cases.

Abnormal Large Platelets Are Associated Not Only with von Willebrand Disease (VWD) Type 2B (Including Type 2B/1 New York) but Also with Severe Type 3: A Potential Role for von Willebrand Factor (VWF) in Megakaryocytopoiesis.

Studies with the Nanobody That Detects the Gain-of-Function of von Willebrand Factor in a Cohort of Patients with Type 2B von Willebrand Disease: Correlation with Platelet Count, VWF Multimers and Molecular Defects.

Molecular Mapping of the Chloride Binding Site in von Willebrand Factor (VWF): Energetics and Conformational Effects on the ADAMTS-13 Interaction with Wild Type and Type 2B R1306W VWF Forms.

Phenotype and genotype of a cohort of families historically diagnosed with type 1 von Willebrand disease in the European study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 von Willebrand Disease (MCMDM-1VWD)

An Association of Candidate Gene Haplotypes and Bleeding Severity in von Willebrand Disease (VWD) Type 2 Pedigrees.

Biochemical Characterization of Recombinant Von Willebrand Factor (VWF) with a Type 2B Mutation (P1337L) Coexpressed with a Type 1 VWF Defect (C275R): A Complex Molecular Defect in a Patient Previously Diagnosed with Type 2A Von Willebrand Disease (VWD).

An association of candidate gene haplotypes and bleeding severity in von Willebrand disease (VWD) type 1 pedigrees

Molecular Characterization of PK-LR Gene in Pyruvate Kinase–Deficient Italian Patients

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