Ivo P. Touw

Rotterdam, ZH, Netherlands

Last Updated: 09/26/2026

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Found 52 publications

Germ line LCP1 mutations cause immunodeficiency with neutropenia, monocytopenia, lymphopenia, and defective cytokinesis.

Germ line LCP1 mutations cause immunodeficiency with neutropenia, monocytopenia, lymphopenia, and defective cytokinesis.

Journal: Blood advances

Published: March 17, 2025

European guidelines on treatment and supportive measures in chronic neutropenias: A consensus between the European Hematology Association and the EuNet-INNOCHRON COST Action based on a systematic evidence review.

European guidelines on treatment and supportive measures in chronic neutropenias: A consensus between the European Hematology Association and the EuNet-INNOCHRON COST Action based on a systematic evidence review.

Journal: HemaSphere

Published: November 03, 2024

Hematological phenotypes in GATA2 deficiency syndrome arise from aging, maladaptation to proliferation, and somatic events.

Hematological phenotypes in GATA2 deficiency syndrome arise from aging, maladaptation to proliferation, and somatic events.

Journal: Blood advances

Published: October 18, 2024

GATA2 heterozygosity causes an epigenetic feedback mechanism resulting in myeloid and erythroid dysplasia.

GATA2 heterozygosity causes an epigenetic feedback mechanism resulting in myeloid and erythroid dysplasia.

Journal: British journal of haematology

Published: April 03, 2024

RUNX1 is required in granulocyte-monocyte progenitors to attenuate inflammatory cytokine production by neutrophils.

RUNX1 is required in granulocyte-monocyte progenitors to attenuate inflammatory cytokine production by neutrophils.

Journal: bioRxiv : the preprint server for biology

Published: February 07, 2023

RUNX1 is required in granulocyte-monocyte progenitors to attenuate inflammatory cytokine production by neutrophils.

RUNX1 is required in granulocyte-monocyte progenitors to attenuate inflammatory cytokine production by neutrophils.

Journal: Genes & development

Published: January 09, 2023

The European Guidelines on Diagnosis and Management of Neutropenia in Adults and Children: A Consensus Between the European Hematology Association and the EuNet-INNOCHRON COST Action.

The European Guidelines on Diagnosis and Management of Neutropenia in Adults and Children: A Consensus Between the European Hematology Association and the EuNet-INNOCHRON COST Action.

Journal: HemaSphere

Published: November 16, 2022

A congenital CSF3R mutation in chronic neutropenia reveals a vital role for a cytokine receptor extracellular hinge motif in the response to granulocyte colony-stimulating factor.

A congenital CSF3R mutation in chronic neutropenia reveals a vital role for a cytokine receptor extracellular hinge motif in the response to granulocyte colony-stimulating factor.

Journal: Pediatric blood & cancer

Published: July 18, 2022

Truncated CSF3 receptors induce pro-inflammatory responses in severe congenital neutropenia.

Truncated CSF3 receptors induce pro-inflammatory responses in severe congenital neutropenia.

Journal: British journal of haematology

Published: July 07, 2022

Gata2-regulated Gfi1b expression controls endothelial programming during endothelial-to-hematopoietic transition.

Gata2-regulated Gfi1b expression controls endothelial programming during endothelial-to-hematopoietic transition.

Journal: Blood advances

Published: May 04, 2022

Co-Occurring CSF3R W791* Germline and Somatic T618I Driver Mutations Induce Early CNL and Clonal Progression to Mixed Phenotype Acute Leukemia.

Co-Occurring CSF3R W791* Germline and Somatic T618I Driver Mutations Induce Early CNL and Clonal Progression to Mixed Phenotype Acute Leukemia.

Journal: Current oncology (Toronto, Ont.)

Published: December 31, 2021

Congenital neutropenia: disease models guiding new treatment strategies.

Congenital neutropenia: disease models guiding new treatment strategies.

Journal: Current opinion in hematology

Published: December 02, 2021

Showing 1-12 of 52

Last Updated: 09/26/2026