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Journal Articles

UPDATE On the RISK of SECONDARY LEUKEMIA In GENETIC SUBGROUPS ( ELANE , HAX1, WAS, G6PC3, p14 ) of CONGENITAL NEUTROPENIA In EUROPE

Cornelia Zeidler, MD, Peter Vandenberghe, MD, PhD, Irina Schäfer, Ludwig Hoy, Martin Zimmermann, PhD, Manuela Germeshausen, PhD, Karl Welte, MD

Blood (2011) 118 (21): 1106.

https://doi.org/10.1182/blood.V118.21.1106.1106

Published: 2011

Journal Articles

Neutrophil Extracellular Traps (NETs) in Patients with Congenital Neutropenia

Christine Happle, Manuela Germeshausen, PhD, Cornelia Zeidler, MD, Karl Welte, MD, Julia Skokowa, MD, PhD

Blood (2011) 118 (21): 15.

https://doi.org/10.1182/blood.V118.21.15.15

Published: 2011

Journal Articles

Update On the Risk of Leukemia in Genetic Subgroups of Congenital Neutropenia (CN): Comparison of Patients with Known Gene Mutations ( ELA2 , HAX1, WASP, G6PC3, p14) .

Cornelia Zeidler, MD, Jean Donadieu, MD, Audrey Anna Bolyard, R.N., B.S., Peter Vandenberghe, MD, PhD, Gusal Pracht, Blandine Beaupain, Ludwig Hoy, Dr.rer.nat., Martin Zimmermann, PhD, Christine Bellanne-Chantelot, Daniel C Link, Christoph Klein, Manuela Germeshausen, PhD, David C. Dale, MD, Karl Welte

Blood (2009) 114 (22): 3597.

https://doi.org/10.1182/blood.V114.22.3597.3597

Published: 2009

Journal Articles

Overexpression of the Differentiation-Defective G-CSF Receptor Isoform IV Is Associated with a High Incidence of Relapses in Childhood Acute Myeloid Leukemia Treated with G-CSF

Stephanie Ehlers, MD, Christin Herbst, Martin Zimmermann, PhD, Nicole Scharn, Manuela Germeshausen, PhD, Claudia Langebrake, PhD, Thomas Lehrnbecher, MD, Jochen Harbott, PhD, Jan Stary, MD, PhD, Michael Dworzak, MD, Ursula Creutzig, MD, Dirk Reinhardt, MD, PhD

Blood (2008) 112 (11): 2528.

https://doi.org/10.1182/blood.V112.11.2528.2528

Published: 2008

Journal Articles

GATA1 Mutations in Transient Leukemia and Myeloid Leukemia in “Down” Syndrome.

Katarina Reinhardt, PhD, Katarina Boehmer, Jan-Henning Klusmann, MD, Manuela Germeshausen, PhD, Annette Sander, MD, Christine von Neuhoff, MD, Jan Stary, MD, PhD, Heribert Jürgens, MD, PhD, Arnulf Pekrun, MD, PhD, Axel Sauerbrey, MD, PhD, Charlotte M Niemeyer, MD, PhD, Gudrun Fleischhack, MD, PhD, Ursula Creutzig, MD, PhD, Dirk Reinhardt, MD, PhD

Blood (2008) 112 (11): 923.

https://doi.org/10.1182/blood.V112.11.923.923

Published: 2008

Journal Articles

Serial Analysis of Hematopoietic Progenitors in Mpl −/− Mice.

Janet Kaffanke, PhD, Manuela Germeshausen, PhD, Karl Welte, MD, Matthias Ballmaier, PhD

Blood (2007) 110 (11): 2100.

https://doi.org/10.1182/blood.V110.11.2100.2100

Published: 2007

Journal Articles

In Vivo Growth Advantage of Cells Expressing Acquired CSF3R Mutations in Patients with Severe Congenital Neutropenia.

Manuela Germeshausen, PhD, Matthias Ballmaier, PhD, Karl Welte, MD

Blood (2007) 110 (11): 3296.

https://doi.org/10.1182/blood.V110.11.3296.3296

Published: 2007

Journal Articles

Defective Expression of Neutrophil Serine Proteases in Myeloid Progenitors of Congenital Neutropenia Patients Carrying Either ELA2 or HAX1 Mutations.

Julia Skokowa, MD, PhD, John-Paul Fobiwe, Dan Lan, Manuela Germeshausen, PhD, Karl Welte, MD PhD

Blood (2007) 110 (11): 3299.

https://doi.org/10.1182/blood.V110.11.3299.3299

Published: 2007

Journal Articles

RAS and G-CSF Receptor Mutations Are Mutually Exclusive in Leukemogenesis in Severe Congenital Neutropenia.

Manuela Germeshausen, PhD, Chris Kratz, MD, Matthias Ballmaier, PhD, Kevin M. Shannon, MD, Karl Welte, MD

Blood (2005) 106 (11): 3073.

https://doi.org/10.1182/blood.V106.11.3073.3073

Published: 2005

Journal Articles

c-mpl Mutations in Congenital Amegakaryocytic Thrombocytopenia: Residual TPO Receptor Activity in Patients of Group CAMT II.

Matthias Ballmaier, PhD, Karl Welte, MD, Manuela Germeshausen, PhD

Blood (2005) 106 (11): 2157.

https://doi.org/10.1182/blood.V106.11.2157.2157

Published: 2005

Journal Articles

Mutations in the Gene of Neutrophil Elastase Associated with Congenital Neutropenia Lead to Alteration of Intracellular Trafficking and Proteolytic Function of NE Protein.

Carmela Beger, MD, Inga Koellner, Cornelia Zeidler, MD, Manuela Germeshausen, PhD, Nils von Neuhoff, PhD, Brigitte Schlegelberger, MD, PhD, Karl Welte, MD, PhD

Blood (2004) 104 (11): 780.

https://doi.org/10.1182/blood.V104.11.780.780

Published: 2004

NARROW

UPDATE On the RISK of SECONDARY LEUKEMIA In GENETIC SUBGROUPS ( ELANE , HAX1, WAS, G6PC3, p14 ) of CONGENITAL NEUTROPENIA In EUROPE

Neutrophil Extracellular Traps (NETs) in Patients with Congenital Neutropenia

Update On the Risk of Leukemia in Genetic Subgroups of Congenital Neutropenia (CN): Comparison of Patients with Known Gene Mutations ( ELA2 , HAX1, WASP, G6PC3, p14) .

Overexpression of the Differentiation-Defective G-CSF Receptor Isoform IV Is Associated with a High Incidence of Relapses in Childhood Acute Myeloid Leukemia Treated with G-CSF

GATA1 Mutations in Transient Leukemia and Myeloid Leukemia in “Down” Syndrome.

Serial Analysis of Hematopoietic Progenitors in Mpl −/− Mice.

In Vivo Growth Advantage of Cells Expressing Acquired CSF3R Mutations in Patients with Severe Congenital Neutropenia.

Defective Expression of Neutrophil Serine Proteases in Myeloid Progenitors of Congenital Neutropenia Patients Carrying Either ELA2 or HAX1 Mutations.

RAS and G-CSF Receptor Mutations Are Mutually Exclusive in Leukemogenesis in Severe Congenital Neutropenia.

c-mpl Mutations in Congenital Amegakaryocytic Thrombocytopenia: Residual TPO Receptor Activity in Patients of Group CAMT II.

Mutations in the Gene of Neutrophil Elastase Associated with Congenital Neutropenia Lead to Alteration of Intracellular Trafficking and Proteolytic Function of NE Protein.

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American Society of Hematology

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ASH Publications

American Society of Hematology

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