Thomas Vraetz

Freiburg, BW, Germany

Last Updated: 09/26/2026

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Found 19 publications

Updated AWMF Guideline on the Diagnosis and Treatment of Langerhans cell Histiocytosis in Children and Adolescents

Updated AWMF Guideline on the Diagnosis and Treatment of Langerhans cell Histiocytosis in Children and Adolescents

Journal: Klinische Padiatrie

Published: September 04, 2023

ORAI1 mutations abolishing store-operated Ca2+ entry cause anhidrotic ectodermal dysplasia with immunodeficiency.

ORAI1 mutations abolishing store-operated Ca2+ entry cause anhidrotic ectodermal dysplasia with immunodeficiency.

Journal: The Journal of allergy and clinical immunology

Published: August 25, 2017

Variable impairment of platelet functions in patients with severe, genetically linked immune deficiencies.

Variable impairment of platelet functions in patients with severe, genetically linked immune deficiencies.

Journal: Haematologica

Published: July 26, 2017

Hematopoietic stem cell transplantation in 29 patients hemizygous for hypomorphic IKBKG/NEMO mutations.

Hematopoietic stem cell transplantation in 29 patients hemizygous for hypomorphic IKBKG/NEMO mutations.

Journal: Blood

Published: March 11, 2017

Hemophagocytic lymphohistiocytosis as presenting manifestation of profound combined immunodeficiency due to an ORAI1 mutation.

Hemophagocytic lymphohistiocytosis as presenting manifestation of profound combined immunodeficiency due to an ORAI1 mutation.

Journal: The Journal of allergy and clinical immunology

Published: November 22, 2016

Transplantation from a symptomatic carrier sister restores host defenses but does not prevent colitis in NEMO deficiency.

Transplantation from a symptomatic carrier sister restores host defenses but does not prevent colitis in NEMO deficiency.

Journal: Clinical immunology (Orlando, Fla.)

Published: October 22, 2015

A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysis.

A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysis.

Journal: The Journal of allergy and clinical immunology

Published: October 09, 2015

SYK expression endows human ZAP70-deficient CD8 T cells with residual TCR signaling.

SYK expression endows human ZAP70-deficient CD8 T cells with residual TCR signaling.

Journal: Clinical immunology (Orlando, Fla.)

Published: May 21, 2015

Omenn syndrome associated with a functional reversion due to a somatic second-site mutation in CARD11 deficiency.

Omenn syndrome associated with a functional reversion due to a somatic second-site mutation in CARD11 deficiency.

Journal: Blood

Published: February 28, 2015

The syndrome of hemophagocytic lymphohistiocytosis in primary immunodeficiencies: implications for differential diagnosis and pathogenesis.

The syndrome of hemophagocytic lymphohistiocytosis in primary immunodeficiencies: implications for differential diagnosis and pathogenesis.

Journal: Haematologica

Published: January 26, 2015

Patients with T⁺/low NK⁺ IL-2 receptor γ chain deficiency have differentially-impaired cytokine signaling resulting in severe combined immunodeficiency.

Patients with T⁺/low NK⁺ IL-2 receptor γ chain deficiency have differentially-impaired cytokine signaling resulting in severe combined immunodeficiency.

Journal: European journal of immunology

Published: March 25, 2014

Hemophagocytic lymphohistiocytosis in imported pediatric visceral leishmaniasis in a nonendemic area.

Hemophagocytic lymphohistiocytosis in imported pediatric visceral leishmaniasis in a nonendemic area.

Journal: The Journal of pediatrics

Published: December 16, 2013

Showing 1-12 of 19

Last Updated: 09/26/2026