I. Fuchs

发表

β2-Microglobulin deficiency causes a complex immunodeficiency of the innate and adaptive immune system.

K. Schwarz, S. Ehl, A. Schmitt-Graeff, 2015, The Journal of allergy and clinical immunology.

Deficiency of caspase recruitment domain family, member 11 (CARD11), causes profound combined immunodeficiency in human subjects.

Anne-Kathrin Kienzler, L. Miosge, A. Enders, 2013, The Journal of allergy and clinical immunology.

CD57 identifies T cells with functional senescence before terminal differentiation and relative telomere shortening in patients with activated PI3 kinase delta syndrome

K. Schwarz, T. Brümmendorf, P. Soler-Palacín, 2018, Immunology and cell biology.

Evolution of disease activity and biomarkers on and off rapamycin in 28 patients with autoimmune lymphoproliferative syndrome

K. Schwarz, F. Rieux-Laucat, A. Fischer, 2017, Haematologica.

Gray platelet syndrome can mimic autoimmune lymphoproliferative syndrome.

U. Pannicke, K. Schwarz, F. Rieux-Laucat, 2015, Blood.

Altered T-Lymphocyte Biology Following High-Dose Melphalan and Autologous Stem Cell Transplantation With Implications for Adoptive T-Cell Therapy

S. Ehl, A. Maghnouj, S. Hahn, 2020, Frontiers in Oncology.

Functional flow cytometry of monocytes for routine diagnosis of innate primary immunodeficiencies.

S. Ehl, S. Fuchs, I. Hainmann, 2019, The Journal of allergy and clinical immunology.

Hyperactive mTOR pathway promotes lymphoproliferation and abnormal differentiation in autoimmune lymphoproliferative syndrome.

K. Schwarz, S. Ehl, A. Mackensen, 2015, Blood.

Effective Immunological Guidance of Genetic Analyses Including Exome Sequencing in Patients Evaluated for Hemophagocytic Lymphohistiocytosis

S. Ehl, H. Hennies, C. Klemann, 2017, Journal of Clinical Immunology.

Novel Patient with Late-Onset Familial Hemophagocytic Lymphohistiocytosis with STXBP2 Mutations Presenting with Autoimmune Hepatitis, Neurological Manifestations and Infections Associated with Hypogammaglobulinemia

S. Ehl, N. Rezaei, S. Ammann, 2014, Journal of Clinical Immunology.

A distinct CD38+CD45RA+ population of CD4+, CD8+, and double-negative T cells is controlled by FAS

K. Schwarz, R. Backofen, M. Boerries, 2020, The Journal of experimental medicine.

Flow Cytometry in the Diagnosis and Follow Up of Human Primary Immunodeficiencies

U. Sack, U. Salzer, I. Fuchs, 2019, EJIFCC.

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.

Primary and secondary hemophagocytic lymphohistiocytosis have different patterns of T‐cell activation, differentiation and repertoire

S. Ehl, C. Klemann, M. Heeg, 2017, European journal of immunology.

Abnormally differentiated CD4+ or CD8+ T cells with phenotypic and genetic features of double negative T cells in human Fas deficiency.

K. Schwarz, H. Pircher, S. Ehl, 2014, Blood.

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.

Sequential decisions on FAS sequencing guided by biomarkers in patients with lymphoproliferation and autoimmune cytopenia

K. Schwarz, W. Vach, E. Mejstrikova, 2013, Haematologica.

Novel Patient with Late-Onset Familial Hemophagocytic Lymphohistiocytosis with STXBP2 Mutations Presenting with Autoimmune Hepatitis, Neurological Manifestations and Infections Associated with Hypogammaglobulinemia

S. Ehl, N. Rezaei, S. Ammann, 2014, Journal of Clinical Immunology.

Abnormally differentiated CD 4 1 or CD 8 1 T cells with phenotypic and genetic features of double negative T cells in human Fas de fi ciency

K. Schwarz, H. Pircher, S. Ehl, 2014 .

Treosulfan-based conditioning in DOCK8 deficiency: complete lympho-hematopoietic reconstitution with minimal toxicity.

A. Borkhardt, Sujal Ghosh, R. Meisel, 2012, Clinical immunology.

Case Report: Hemophagocytic Lymphohistiocytosis and Non-Tuberculous Mycobacteriosis Caused by a Novel GATA2 Variant

S. Ehl, K. Warnatz, R. Schroers, 2021, Frontiers in Immunology.