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Journal Articles

N ovel Splice-Site Mutation in RASGRP2 Leading to Caldag-GEFI Deficiency

Doris Boeckelmann, PhD, Antonia Lenz, MS, Salome Fels, MS, Felicia Loewecke, MD, Ekkehart Lausch, MD, Barbara Zieger, MD

Blood (2020) 136 (Supplement 1): 16–17.

https://doi.org/10.1182/blood-2020-139153

Published: 2020

Journal Articles

Improved Values for Acquired Von Willebrand Syndrome and Better Clinical Outcome in Patients with Heartmate III Compared to Heartmate II

Ulrich Geisen, MD, Kerstin Brehm, MD, Georg Trummer, MD, Friedhelm Beyersdorf, MD, Michael Berchtold-Herz, MD, Claudia Heilmann, MD, Johannes Schelling, MD, Axel Schlagenhauf, PhD, Barbara Zieger, MD

Blood (2016) 128 (22): 2582.

https://doi.org/10.1182/blood.V128.22.2582.2582

Published: 2016

Journal Articles

Patients with Hermansky-Pudlak Syndrome Show Various Phenotypes Caused by Novel Mutations,

Kirstin Sandrock, PhD, Karin Kurnik, MD, Stephan Ehl, MD, Christoph Bidlingmaier, Lea Nakamura, Nina Rombach, MD, Sophie Schäfer, MD, Barbara Zieger, MD

Blood (2011) 118 (21): 3286.

https://doi.org/10.1182/blood.V118.21.3286.3286

Published: 2011

Journal Articles

International Consortium for the Study of Clinical and Molecular Aspects of Bernard-Soulier Syndrome

Anna Savoia, PhD, Shinji Kunishima, PhD, Patrizia Noris, MD, Nuria Pujol-Moix, MD, Dermot Kenny, MD, Nurit Rosenberg, Margaret L. Rand, PhD, Barbara Zieger, MD, Ali F. Gargouri, PhD, Miriam P Beltrame, Felisa C. Molinas, MD, PhD, Mehran Karimi, MD, Christopher Ward, MB, CHB, PhD, Philip Kuriakose, MD, Nadia Ewing, MD, Carol Diamond, MD, Alok Srivastava, MD, Carlo Luigi Balduini, MD, Francois Lanza, PhD, MD

Blood (2011) 118 (21): 707.

https://doi.org/10.1182/blood.V118.21.707.707

Published: 2011

Journal Articles

European Collaborative Paediatric Database on Cerebral Venous Thrombosis: Risk Factors for Recurrent Venous Thromboembolism.

Gili Kenet, MD, Fenella Kirkham, MD, Thomas Niederstadt, MD, Karin Kurnik, MD, Rosemarie Schobess, MD, Ralf Knofler, MD, Barbara Zieger, MD, Ulrike Nowak-Gottl, MD

Blood (2006) 108 (11): 276.

https://doi.org/10.1182/blood.V108.11.276.276

Published: 2006

Journal Articles

Deletion of Two Contiguous Genes, Platelet GPIbβ (Glycoprotein Ibβ) and Septin SEPT5, in a Boy with Bernard-Soulier Syndrome and Developmental Delay: A Possible New Contiguous Gene Syndrome.

Ingrid Bartsch, PhD, Ina Hainmann, MD, Susanne Bläser, PhD, Anna Pavlova, MD, Johannes Oldenburg, MD, Anja Busse, Francois Lanza, PhD, Paquita Nurden, MD, PhD, Andrea Superti-Furga, MD, Barbara Zieger, MD

Blood (2006) 108 (11): 1097.

https://doi.org/10.1182/blood.V108.11.1097.1097

Published: 2006

Journal Articles

SEPT11, a Novel Platelet Septin Partners with the Platelet Septin SEPT5.

Sabrina Röseler, Susanne Bläser, PhD, Ingrid Bartsch, PhD, Hansjörg Rempp, Heike Bauer, Mareike Lieber, Anja Busse, Barbara Zieger, MD

Blood (2005) 106 (11): 3945.

https://doi.org/10.1182/blood.V106.11.3945.3945

Published: 2005

Journal Articles

Mutations in the VKORC1 Gene Cause Warfarin Resistance, Warfarin Sensitivity and Combined Deficiency of Vitamin K Dependent Coagulation Factors.

Johannes Oldenburg, MD, PhD, Simone Rost, Andreas Fregin, PhD, Christof Geisen, Vytautas Ivaskevicius, MD, Erhard Seifried, MD, Inge Scharrer, MD, Maximilian Heistinger, MD, Edward Tuddenham, MD, Clemens Muller-Reible, PhD, Barbara Zieger, MD

Blood (2004) 104 (11): 277.

https://doi.org/10.1182/blood.V104.11.277.277

Published: 2004

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N ovel Splice-Site Mutation in RASGRP2 Leading to Caldag-GEFI Deficiency

Improved Values for Acquired Von Willebrand Syndrome and Better Clinical Outcome in Patients with Heartmate III Compared to Heartmate II

Patients with Hermansky-Pudlak Syndrome Show Various Phenotypes Caused by Novel Mutations,

International Consortium for the Study of Clinical and Molecular Aspects of Bernard-Soulier Syndrome

European Collaborative Paediatric Database on Cerebral Venous Thrombosis: Risk Factors for Recurrent Venous Thromboembolism.

Deletion of Two Contiguous Genes, Platelet GPIbβ (Glycoprotein Ibβ) and Septin SEPT5, in a Boy with Bernard-Soulier Syndrome and Developmental Delay: A Possible New Contiguous Gene Syndrome.

SEPT11, a Novel Platelet Septin Partners with the Platelet Septin SEPT5.

Mutations in the VKORC1 Gene Cause Warfarin Resistance, Warfarin Sensitivity and Combined Deficiency of Vitamin K Dependent Coagulation Factors.

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