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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

Novel Insights into the Clinical Phenotype and Pathophysiology Underlying Low VWF Levels: The Low Von Willebrand Factor in Ireland Cohort (LoVIC) Study

Michelle Lavin, MB FRCPath, Sonia Aguila, PhD, Sonja Schneppenheim, MD, Niall Dalton, BSc, Jamie M O'Sullivan, PhD, Niamh M O'Connell, MB, FRCPath, PhD, Kevin M. Ryan, MB, Mary Byrne, MSc, Margaret Nolan, BSc, Roger Preston, PhD, Ulrich Budde, MD, Paula D. James, MD, Jorge Di Paola, MD, James S O'Donnell, MD PhD

Blood (2016) 128 (22): 873.

https://doi.org/10.1182/blood.V128.22.873.873

Published: 2016

Journal Articles

The Acquired Von Willebrand Syndrome in Patients with Monoclonal IgA Proteins Is Rare but May be Clinically Severe

Ulrich Budde, MD, Rita Dittmer, MD, Sonja Schneppenheim, MD, Tina Rausch

Blood (2014) 124 (21): 2830.

https://doi.org/10.1182/blood.V124.21.2830.2830

Published: 2014

Journal Articles

Spectrum Of The Acquired Von Willebrand Syndrome In a Large Cohort Of Patients Diagnosed In a Single Institution

Ulrich Budde, MD, Rita Dittmer, Hala El- Abd Müller, Hanna Schaeper, Sonja Schneppenheim, MD

Blood (2013) 122 (21): 3607.

https://doi.org/10.1182/blood.V122.21.3607.3607

Published: 2013

Journal Articles

Frequency and Determinants of Thrombotic and Bleeding Complications in Ph Negative Myeloproliferative Neoplasms (MPN): The Role of Adamts-13 and VWF Activities in an Italian Cohort 0f 88 Well Characterized Patients

Augusto B. Federici, MD, Maria C Carraro, Antonella Lattuada, Chiara Vanelli, Veronica Sciumbata, Valentina Rossi, MD, Daniela Intini, Sarah Birindelli, Sara Munizza, Elisabetta Sacchi, Umberto Russo, Ulrich Budde, MD

Blood (2012) 120 (21): 3369.

https://doi.org/10.1182/blood.V120.21.3369.3369

Published: 2012

Journal Articles

Characterization of the p.A1461D Mutation Causing Von Willebrand's Disease Type 2B with Severe Thrombocytopenia, Circulating Giant Platelets and Defective α -Granule Secretion

Florian Langer, MD, Tobias Obser, Florian Oyen, Katharina Holstein, MD, Brigitte Spath, Andreas Greinacher, MD, Ulrich Budde, MD, Carsten Bokemeyer, Reinhard Schneppenheim, MD, PhD

Blood (2012) 120 (21): 1074.

https://doi.org/10.1182/blood.V120.21.1074.1074

Published: 2012

Journal Articles

Subcellular Localization of Von Willebrand Factor Mutants Correlates with Particular VWF Multimer Patterns

Maria A. Brehm, PhD, Tobias Obser, Ulrich Budde, MD, Sonja Schneppenheim, MD, Reinhard Schneppenheim, MD, PhD

Blood (2012) 120 (21): 98.

https://doi.org/10.1182/blood.V120.21.98.98

Published: 2012

Journal Articles

Intracellular Retention, Enhanced Clearance, and Defective FVIII Binding Are Common Features of Von Willebrand Factor D'-D3 Domain Mutations in Patients with Von Willebrand Disease Type 1 From the European Mcmdm-1VWD Study

Reinhard Schneppenheim, MD, PhD, Ulrich Budde, MD, Javier Batlle, MD, Giancarlo Castaman, MD, Jeroen C. J. Eikenboom, MD, PhD, Augusto B. Federici, MD, Jenny Goudemand, MD, PhD, Tobias Obser, Florian Oyen, Francesco Rodeghiero, MD, Sonja Schneppenheim, MD, Ian R. Peake, PhD, Anne C. Goodeve, PhD

Blood (2012) 120 (21): 99.

https://doi.org/10.1182/blood.V120.21.99.99

Published: 2012

Journal Articles

A Novel Missense Mutation Asp69Gly in the Platelet Glycoprotein Ib(beta) Gene in Two Families with Bernard-Soulier Syndrome,

Wolf A Hassenpflug, MD, Belinda Weber, Tobias Obser, Ulrich Budde, MD, Reinhard Schneppenheim, MD, PhD

Blood (2011) 118 (21): 3300.

https://doi.org/10.1182/blood.V118.21.3300.3300

Published: 2011

Journal Articles

Long-Term Prophylaxis In Children, Adolescents and Young Adults with Von Willebrand Disease – First Results of a Cohort Study

Susan Halimeh, MD, Anne Kruempel, Hannelore Rott, Nadja Bogdanova, Ulrich Budde, MD, Daniela Manner, Britta Faeser, Rolf M. Mesters, Ulrike Nowak-Gottl, MD

Blood (2010) 116 (21): 714.

https://doi.org/10.1182/blood.V116.21.714.714

Published: 2010

Journal Articles

Force Dependent Structural Changes of the Von Willebrand Factor A2 Domain Are Required for VWF Cleavage by ADAMTS13

Reinhard Schneppenheim, MD, PhD, Carsten Baldauf, PhD, Tobias Obser, Ulrich Budde, MD, Antje Pieconka, Sonja Schneppenheim, MD, Frauke Graeter, PhD

Blood (2008) 112 (11): 589.

https://doi.org/10.1182/blood.V112.11.589.589

Published: 2008

Journal Articles

Molecular Background of “Smeary” von Willebrand Factor Multimers.

Reinhard Schneppenheim, MD, PhD, Olivier Marggraf, Heike Eckert, Tobias Obser, Florian Oyen, Antje Pieconka, Sonja Schneppenheim, MD, Kerstin Will, Ulrich Budde, MD

Blood (2007) 110 (11): 2711.

https://doi.org/10.1182/blood.V110.11.2711.2711

Published: 2007

Journal Articles

A Pathophysiological Role for ADAMTS13 in Thrombotic Thrombocytopenic Purpura (TTP) without Severe ADAMTS13 Deficiency.

Johanna A. Kremer Hovinga, MD, James N. George, MD, Sara K. Vesely, PhD, Deirdre R. Terrell, MPH, Ulrich Budde, MD, Irmela Sulzer, Bernhard Lammle, MD

Blood (2006) 108 (11): 1068.

https://doi.org/10.1182/blood.V108.11.1068.1068

Published: 2006

Journal Articles

A Novel Mutation in the von Willebrand Factor Propeptide Causes Defective Regulated Storage in Platelets and Weibel-Palade Bodies.

Sandra L. Haberichter, PhD, Ulrich Budde, MD, Elke Drewke, Tobias Obser, Cornelia Wermes, MD, Reinhard Schneppenheim, M.D, Ph.D

Blood (2005) 106 (11): 1007.

https://doi.org/10.1182/blood.V106.11.1007.1007

Published: 2005

Journal Articles

Human Thrombospondin-1 in Eleven von Willebrand Factor /FVIII Coagulation Factor Concentrates.

Tobias M. Suiter, MD, PhD, Ulrich Budde, MD, PhD

Blood (2005) 106 (11): 4031.

https://doi.org/10.1182/blood.V106.11.4031.4031

Published: 2005

Journal Articles

Familial Thrombotic Thrombocytopenic Purpura in Three Siblings.

Edyta Niewiadomska, MD, Ulrich Budde, MD, Klukowska Anna

Blood (2005) 106 (11): 4042.

https://doi.org/10.1182/blood.V106.11.4042.4042

Published: 2005

Journal Articles

High Shear Stress and Immobilization of Von Willebrand Factor Promotes the VWF-Cleaving Protease Activity as Assessed by the Cone and Plate(let) Analyzer.

David Varon, MD, Boris Shenkman, MD, PhD, Ulrich Budde, MD, Dorothea Angerhaus, PhD, Reinhard Schneppenheim, MD, Naphtali Savion, PhD, Uri Seligsohn, MD

Blood (2004) 104 (11): 849.

https://doi.org/10.1182/blood.V104.11.849.849

Published: 2004

Journal Articles

Distinction of Inherited from Acquired Thrombotic Thrombocytopenic Purpura Applying the Cone and Plate(Let) Analyzer.

Boris Shenkman, MD, PhD, Ulrich Budde, MD, Dorothea Angerhaus, PhD, Reinhard Schneppenheim, MD, Aharon Lubetsky, MD, Naphtali Savion, PhD, Uri Seligsohn, MD, David Varon, MD

Blood (2004) 104 (11): 853.

https://doi.org/10.1182/blood.V104.11.853.853

Published: 2004

Journal Articles

Inhibitor Incidence in Previously Untreated Patients (PUP) with Hemophilia A and B - a 10-Year-Follow up of the Prospective Multicenter Study.

Wolfhart Kreuz, MD, Guenter K.H. Auerswald, MD, Ulrich Budde, MD, Harald Lenk, MD

Blood (2004) 104 (11): 3983.

https://doi.org/10.1182/blood.V104.11.3983.3983

Published: 2004

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.

Novel Insights into the Clinical Phenotype and Pathophysiology Underlying Low VWF Levels: The Low Von Willebrand Factor in Ireland Cohort (LoVIC) Study

The Acquired Von Willebrand Syndrome in Patients with Monoclonal IgA Proteins Is Rare but May be Clinically Severe

Spectrum Of The Acquired Von Willebrand Syndrome In a Large Cohort Of Patients Diagnosed In a Single Institution

Frequency and Determinants of Thrombotic and Bleeding Complications in Ph Negative Myeloproliferative Neoplasms (MPN): The Role of Adamts-13 and VWF Activities in an Italian Cohort 0f 88 Well Characterized Patients

Characterization of the p.A1461D Mutation Causing Von Willebrand's Disease Type 2B with Severe Thrombocytopenia, Circulating Giant Platelets and Defective α -Granule Secretion

Subcellular Localization of Von Willebrand Factor Mutants Correlates with Particular VWF Multimer Patterns

Intracellular Retention, Enhanced Clearance, and Defective FVIII Binding Are Common Features of Von Willebrand Factor D'-D3 Domain Mutations in Patients with Von Willebrand Disease Type 1 From the European Mcmdm-1VWD Study

A Novel Missense Mutation Asp69Gly in the Platelet Glycoprotein Ib(beta) Gene in Two Families with Bernard-Soulier Syndrome,

Long-Term Prophylaxis In Children, Adolescents and Young Adults with Von Willebrand Disease – First Results of a Cohort Study

Force Dependent Structural Changes of the Von Willebrand Factor A2 Domain Are Required for VWF Cleavage by ADAMTS13

Molecular Background of “Smeary” von Willebrand Factor Multimers.

A Pathophysiological Role for ADAMTS13 in Thrombotic Thrombocytopenic Purpura (TTP) without Severe ADAMTS13 Deficiency.

A Novel Mutation in the von Willebrand Factor Propeptide Causes Defective Regulated Storage in Platelets and Weibel-Palade Bodies.

Human Thrombospondin-1 in Eleven von Willebrand Factor /FVIII Coagulation Factor Concentrates.

Familial Thrombotic Thrombocytopenic Purpura in Three Siblings.

High Shear Stress and Immobilization of Von Willebrand Factor Promotes the VWF-Cleaving Protease Activity as Assessed by the Cone and Plate(let) Analyzer.

Distinction of Inherited from Acquired Thrombotic Thrombocytopenic Purpura Applying the Cone and Plate(Let) Analyzer.

Inhibitor Incidence in Previously Untreated Patients (PUP) with Hemophilia A and B - a 10-Year-Follow up of the Prospective Multicenter Study.

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American Society of Hematology

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American Society of Hematology

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