T. Vraetz

P. Heinrich, T. Ittel, L. Graeve, 1999, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

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

K. Schwarz, A. Fischer, A. Schulz, 2017, The Journal of allergy and clinical immunology.

A prospective evaluation of degranulation assays in the rapid diagnosis of familial hemophagocytic syndromes.

S. Ehl, N. Binder, L. Moretta, 2012, Blood.

Platelet secretion defect in patients with familial hemophagocytic lymphohistiocytosis type 5 (FHL-5).

S. Ehl, B. Zieger, K. Beutel, 2010, Blood.

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

F. Rieux-Laucat, C. Picard, S. Ehl, 2017, The Journal of allergy and clinical immunology.

X-linked inhibitor of apoptosis (XIAP) deficiency: the spectrum of presenting manifestations beyond hemophagocytic lymphohistiocytosis.

K. Schwarz, S. Ehl, H. von Bernuth, 2013, Clinical immunology.

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

U. Pannicke, K. Schwarz, S. Ehl, 2015, Blood.

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

W. Al-Herz, A. Gennery, S. Pai, 2015, Haematologica.

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

W. Behnisch, S. Ehl, C. Bogdan, 2014, The Journal of pediatrics.

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

K. Schwarz, A. Gennery, S. Ehl, 2014, European journal of immunology.

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

K. Schwarz, S. Ehl, S. Feske, 2017, The Journal of allergy and clinical immunology.

Platelet secretion defect in a patient with stromal interaction molecule 1 deficiency.

S. Ehl, J. Heemskerk, C. Speckmann, 2013, Blood.

Prolonged KI Polyomavirus Infection in Immunodeficient Child

M. Panning, B. Strahm, D. Neumann-Haefelin, 2012, Emerging infectious diseases.

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

K. Schwarz, A. Fischer, C. Picard, 2015, Clinical immunology.

Interferon- (cid:1) Sensitizes Resistant Ewing’s Sarcoma Cells to Tumor Necrosis Factor Apoptosis-Inducing Ligand-Induced Apoptosis by Up-Regulation of Caspase-8 Without Altering Chemosensitivity

Lauren Long, C. Niemeyer, U. Kontny, 2007 .

Clinical Heterogeneity of Immunodysregulation, Polyendocrinopathy, Enteropathy, X-linked: Pulmonary Involvement as a Non-Classical Disease Manifestation

K. Schwarz, S. Ehl, I. Schulze, 2014, Journal of Clinical Immunology.

Clinical Heterogeneity of Immunodysregulation, Polyendocrinopathy, Enteropathy, X-linked: Pulmonary Involvement as a Non-Classical Disease Manifestation

K. Schwarz, S. Ehl, I. Schulze, 2014, Journal of Clinical Immunology.

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

K. Schwarz, A. Gennery, S. Ehl, 2014, European journal of immunology.