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Journal Articles

Glucagon-like peptide 2 for intestinal stem cell and Paneth cell repair during graft-versus-host disease in mice and humans

Blood (2020) 136 (12): 1442–1455.

https://doi.org/10.1182/blood.2020005957

Published: 2020

Includes: Supplemental data

Journal Articles

Nonpermissive bone marrow environment impairs early B-cell development in common variable immunodeficiency

Blood (2020) 135 (17): 1452–1457.

https://doi.org/10.1182/blood.2019003855

Published: 2020

Includes: Supplemental data

Journal Articles

The architecture of the IgG anti-carbohydrate repertoire in primary antibody deficiencies

Peter Jandus, Kayluz Frias Boligan, David F. Smith, Elisabeth de Graauw, Bodo Grimbacher, Camilla Jandus, Mai M. Abdelhafez, Alain Despont, Nicolai Bovin, Dagmar Simon, Robert Rieben, Hans-Uwe Simon, Richard D. Cummings, Stephan von Gunten

Blood (2019) 134 (22): 1941–1950.

https://doi.org/10.1182/blood.2019001705

Published: 2019

Includes: Supplemental data

Journal Articles

Common Variable Immunodeficiency (CVID) in Adults As First Manifestation of (cryptic) Dyskeratosis Congenita

Benjamin Rolles, MD, Alla Bulashevska, PhD, Michele Proietti, MD, Sigune Goldacker, MD, Klaus Warnatz, MD, Nadezhda Camacho-Ordonez, MD, Margherita Vieri, MSc, Martin Kirschner, MD, Tim H Brümmendorf, MD, Bodo Grimbacher, MD, Fabian Beier, MD

Blood (2019) 134 (Supplement_1): 1217.

https://doi.org/10.1182/blood-2019-128915

Published: 2019

Journal Articles

Signaling mechanisms inducing hyporesponsiveness of phagocytes during systemic inflammation

Nicole Freise, Alina Burghard, Theresa Ortkras, Niklas Daber, Achmet Imam Chasan, Saskia-L. Jauch, Olesja Fehler, Julia Hillebrand, Mosab Schakaki, Jessica Rojas, Bodo Grimbacher, Thomas Vogl, Andreas Hoffmeier, Sven Martens, Johannes Roth, Judith Austermann

Blood (2019) 134 (2): 134–146.

https://doi.org/10.1182/blood.2019000320

Published: 2019

Includes: Supplemental data

Journal Articles

Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype

Blood (2016) 127 (25): 3154–3164.

https://doi.org/10.1182/blood-2015-11-679902

Published: 2016

Includes: Supplemental data

Journal Articles

The phenotype of human STK4 deficiency

Hengameh Abdollahpour, Giridharan Appaswamy, Daniel Kotlarz, Jana Diestelhorst, Rita Beier, Alejandro A. Schäffer, E. Michael Gertz, Axel Schambach, Hans H. Kreipe, Dietmar Pfeifer, Karin R. Engelhardt, Nima Rezaei, Bodo Grimbacher, Sabine Lohrmann, Roya Sherkat, Christoph Klein

Blood (2012) 119 (15): 3450–3457.

https://doi.org/10.1182/blood-2011-09-378158

Published: 2012

Includes: Supplemental data

Journal Articles

The Phenotype of Human STK4 Deficiency

Hengameh Abdollahpour, MD, PhD, Giridharan Appaswamy, PhD, Rita Beier, MD, Alejandro A. Schäffer, PhD, E. Michael Gertz, PhD, Hans H. Kreipe, MD, Dietmar Pfeifer, PhD, Bodo Grimbacher, MD, Sabine Lohrmann, MD, Roya Sherkat, MD, Christoph Klein, MD, PhD

Blood (2011) 118 (21): 692.

https://doi.org/10.1182/blood.V118.21.692.692

Published: 2011

Journal Articles

Successful Allogeneic Hematopoietic Stem Cell Transplantation for Severe Inflammatory Bowel Disease – IL10 Receptor Deficiency May Serve as a Novel Therapeutic Paradigm

Rita Beier, Daniel Kotlarz, Kaan Boztug, Erik Glocker, Eva Doreen Pfister, Jana Diestelhorst, Dhaarini Murugan, Ulrich Baumann, Sibylle Koletzko, Axel Sauerbrey, Stephan Bruderus, Bodo Grimbacher, Martin G. Sauer, MD, Karl-Walter Sykora, Christoph Klein

Blood (2010) 116 (21): 2379.

https://doi.org/10.1182/blood.V116.21.2379.2379

Published: 2010

Journal Articles

Severe Early-Onset Inflammatory Bowel Disease Caused by IL10 Receptor Deficiency Can Be Cured by Allogeneic Hematopoietic Stem Cell Transplantation.

Blood (2009) 114 (22): 713.

https://doi.org/10.1182/blood.V114.22.713.713

Published: 2009

Journal Articles

Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes

Blood (2009) 113 (9): 1967–1976.

https://doi.org/10.1182/blood-2008-02-141937

Published: 2009

Includes: Supplemental data

Journal Articles

A Novel Clinical Syndrome Associating Severe Congenital Neutropenia and Complex Developmental Aberrations Caused by Deficiency of G6PC3

Blood (2008) 112 (11): 5.

https://doi.org/10.1182/blood.V112.11.5.5

Published: 2008

Journal Articles

Common variable immunodeficiency disorders: division into distinct clinical phenotypes

Helen Chapel, Mary Lucas, Martin Lee, Janne Bjorkander, David Webster, Bodo Grimbacher, Claire Fieschi, Vojtech Thon, Mohammad R. Abedi, Lennart Hammarstrom

Blood (2008) 112 (2): 277–286.

https://doi.org/10.1182/blood-2007-11-124545

Published: 2008

Includes: Supplemental data

Journal Articles

Novel HAX1 mutations in patients with severe congenital neutropenia reveal isoform-dependent genotype-phenotype associations

Manuela Germeshausen, Magda Grudzien, Cornelia Zeidler, Hengameh Abdollahpour, Sevgi Yetgin, Nima Rezaei, Matthias Ballmaier, Bodo Grimbacher, Karl Welte, Christoph Klein

Blood (2008) 111 (10): 4954–4957.

https://doi.org/10.1182/blood-2007-11-120667

Published: 2008

Journal Articles

Identification of a homozygous deletion in the AP3B1 gene causing Hermansky-Pudlak syndrome, type 2

Johannes Jung, Georg Bohn, Anna Allroth, Kaan Boztug, Gudrun Brandes, Inga Sandrock, Alejandro A. Schäffer, Chozhavendan Rathinam, Inga Köllner, Carmela Beger, Reinhard Schilke, Karl Welte, Bodo Grimbacher, Christoph Klein

Blood (2006) 108 (1): 362–369.

https://doi.org/10.1182/blood-2005-11-4377

Published: 2006

Includes: Supplemental data

Journal Articles

Human ICOS deficiency abrogates the germinal center reaction and provides a monogenic model for common variable immunodeficiency

Klaus Warnatz, Lukas Bossaller, Ulrich Salzer, Andrea Skrabl-Baumgartner, Wolfgang Schwinger, Mirjam van der Burg, Jacques J. M. van Dongen, Marzena Orlowska-Volk, Rolf Knoth, Anne Durandy, Ruth Draeger, Michael Schlesier, Hans Hartmut Peter, Bodo Grimbacher

Blood (2006) 107 (8): 3045–3052.

https://doi.org/10.1182/blood-2005-07-2955

Published: 2006

Includes: Supplemental data

Journal Articles

A Variant of Congenital Neutropenia Is Caused by a 3′-UTR Mutation in the Gene Encoding the Endosomal Adaptor Protein p14 ( MAPBPIP ).

Georg Bohn, MD, Anna Allroth, Jens Thiel, MD, Alejandro A. Schäffer, Gudrun Brandes, MD, Erik Glocker, David Teis, PhD, Nicole Taub, Cornelia Zeidler, MD, Robert Geffers, PhD, Jan Buer, MD, Lukas A. Huber, MD/PhD, Karl Welte, MD/PhD, Bodo Grimbacher, MD, Christoph Klein, MD/PhD

Blood (2005) 106 (11): 92.

https://doi.org/10.1182/blood.V106.11.92.92

Published: 2005

NARROW

Glucagon-like peptide 2 for intestinal stem cell and Paneth cell repair during graft-versus-host disease in mice and humans

Nonpermissive bone marrow environment impairs early B-cell development in common variable immunodeficiency

The architecture of the IgG anti-carbohydrate repertoire in primary antibody deficiencies

Common Variable Immunodeficiency (CVID) in Adults As First Manifestation of (cryptic) Dyskeratosis Congenita

Signaling mechanisms inducing hyporesponsiveness of phagocytes during systemic inflammation

Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype

The phenotype of human STK4 deficiency

The Phenotype of Human STK4 Deficiency

Successful Allogeneic Hematopoietic Stem Cell Transplantation for Severe Inflammatory Bowel Disease – IL10 Receptor Deficiency May Serve as a Novel Therapeutic Paradigm

Severe Early-Onset Inflammatory Bowel Disease Caused by IL10 Receptor Deficiency Can Be Cured by Allogeneic Hematopoietic Stem Cell Transplantation.

Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes

A Novel Clinical Syndrome Associating Severe Congenital Neutropenia and Complex Developmental Aberrations Caused by Deficiency of G6PC3

Common variable immunodeficiency disorders: division into distinct clinical phenotypes

Novel HAX1 mutations in patients with severe congenital neutropenia reveal isoform-dependent genotype-phenotype associations

Identification of a homozygous deletion in the AP3B1 gene causing Hermansky-Pudlak syndrome, type 2

Human ICOS deficiency abrogates the germinal center reaction and provides a monogenic model for common variable immunodeficiency

A Variant of Congenital Neutropenia Is Caused by a 3′-UTR Mutation in the Gene Encoding the Endosomal Adaptor Protein p14 ( MAPBPIP ).

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American Society of Hematology

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American Society of Hematology

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