Ehl, Stephan
Stephan Ehl researcher
VIAF ID: 7676152503065910800007 (Personal)
Permalink: http://viaf.org/viaf/7676152503065910800007
Preferred Forms
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- 100 1 _ ‡a Ehl, Stephan
- 100 1 _ ‡a Ehl, Stephan
- 100 0 _ ‡a Stephan Ehl ‡c researcher
4xx's: Alternate Name Forms (4)
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Works
Title | Sources |
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Agammaglobulinemia with normal B-cell numbers in a patient lacking Bob1 | |
Altered t-lymphocyte biology following high-dose melphalan and autologous stem cell transplantation with implications for adoptive t-cell therapy | |
Autoimmune lymphoproliferative immunodeficiencies (ALPID) in childhood: breakdown of immune homeostasis and immune dysregulation | |
autoimmune targets in IPEX are dominated by gut epithelial proteins | |
BCL10 deficiency presenting as severe combined immunodeficiency escaping newborn screening | |
burden of common variable immunodeficiency disorders: a retrospective analysis of the European Society for Immunodeficiency (ESID) registry data | |
Case report: Hemophagocytic lymphohistiocytosis and non-tuberculous mycobacteriosis caused by a novel GATA2 variant | |
Cell versus cytokine – directed therapies for hemophagocytic lymphohistiocytosis (HLH) in inborn errors of immunity | |
Clinical spectrum and features of activated phosphoinositide 3-kinase δ syndrome: a large patient cohort study | |
Corrigendum: Clinical and molecular heterogeneity of RTEL1 deficiency | |
Curative treatment of POMP-related autoinflammation and immune dysregulation (PRAID) by hematopoietic stem cell transplantation | |
Differences in granule morphology yet equally impaired exocytosis among cytotoxic T cells and NK cells from Chediak–Higashi syndrome patients | |
Disease evolution and response to rapamycin in activated phosphoinositide 3-kinase [delta] syndrome: the european society for immunodeficiencies-activated phosphoinositide 3-kinase [delta] syndrome registry | |
Disease progression of WHIM syndrome in an international cohort of 66 pediatric and adult patients | |
A distinct CD38+CD45RA+ population of CD4+, CD8+, and double-negative T cells is controlled by FAS | |
Dysregulated PI3K signaling in B cells of CVID patients | |
Early-onset autoimmunity associated with SOCS1 haploinsufficiency | |
Early‐onset, fatal interstitial lung disease in STAT3 gain‐of‐function patients | |
Enabling external inquiries to an existing patient registry by using the open source registry system for rare diseases: demonstration of the system using the European Society for Immunodeficiencies registry | |
Establishing the molecular diagnoses in a cohort of 291 patients with predominantly antibody deficiency by targeted next-generation sequencing: Experience from a monocentric study | |
Evolution of disease activity and biomarkers on and off rapamycin in 28 patients with autoimmune lymphoproliferative syndrome | |
GAIN Registry - a new prospective study for patients with multi-organ autoimmunity and autoinflammation | |
Gene editing of hematopoietic stem cells restores T cell response in familial hemophagocytic lymphohistiocytosis | |
Genetic, phenotypic and functional characterization of a cohort of patients with EBV-associated T/NK lymphoproliferations | |
German national registry of primary immunodeficiencies (2012–2017) | |
Germline biallelic PIK3CG mutations in a multifaceted immunodeficiency with immune dysregulation : letter to the editor | |
Germline STAT3 gain-of-function mutations in primary immunodeficiency: Impact on the cellular and clinical phenotype | |
Griscelli syndrome type 2 sine albinism: unraveling differential RAB27A effector engagement | |
Hemophagocytic lymphohistiocytosis in adults: collaborative analysis of 137 cases of a nationwide German registry | |
Hermansky-Pudlak Syndrome: identification of novel variants in the genes HPS3, HPS5, and DTNBP1 (HPS-7) | |
High-dimensional profiling reveals Tc17 cell enrichment in active Crohn’s disease and identifies a potentially targetable signature | |
High levels of IL-18 and IFN-γ in chronically inflamed tissue in chronic granulomatous disease | |
Hospital acquired infections and their investigation – dealing with the impact of time in hospital epidemiology | |
Immune dysregulation in patients with PTEN hamartoma tumor syndrome: analysis of FOXP3 regulatory T cells | |
Immune‐mediated pathology as a consequence of impaired immune reactions: the IMPATH paradox | |
Immunodeficiency with susceptibility to lymphoma with complex genotype affecting energy metabolism (FBP1, ACAD9) and vesicle trafficking (RAB27A) | |
Immunomodulatory effects of different Cannabis extracts on human primary lymphocytes | |
Immunopathology caused by impaired CD8+ T‐cell responses | |
Impaired IL-23–dependent induction of IFN-γ underlies mycobacterial disease in patients with inherited TYK2 deficiency | |
International retrospective study of allogeneic hematopoietic cell transplantation for activated PI3K-delta syndrome | |
JAKi salvage therapy followed by curative cord blood transplantation in a XIAP-deficient infant with relapsing HLH | |
Json2Xlsx: extraction and visualization of nested data in a sparse spreadsheet | |
Ledipasvir/Sofosbuvir eradicates hepatitis C in an immunodeficient STAT3-GOF patient | |
Long-term follow-up of IPEX syndrome patients after different therapeutic strategies: An international multicenter retrospective study | |
Long-term robustness of a T-cell system emerging from somatic rescue of a genetic block in T-cell development | |
MAP kinase activating death domain deficiency is a novel cause of impaired lymphocyte cytotoxicity | |
Modeling MyD88 deficiency in vitro provides new insights in Its function | |
NCKAP1L defects lead to a novel syndrome combining immunodeficiency, lymphoproliferation, and hyperinflammation | |
Prevalence and clinical challenges among adults with primary immunodeficiency and recombination-activating gene deficiency | |
Prospective newborn screening for SCID in Germany: A first analysis by the pediatric immunology working group (API) | |
A RAB27A 5′ untranslated region structural variant associated with late-onset hemophagocytic lymphohistiocytosis and normal pigmentation | |
Rapid identification and characterization of infected cells in blood during chronic active Epstein-Barr virus infection | |
RLTPR deficiency : a new genetic etiology of combined immunodeficiency | |
Simple measurement of IgA predicts immunity and mortality in Ataxia-Telangiectasia | |
T-cell gene therapy for perforin deficiency corrects cytotoxicity defects and prevents hemophagocytic lymphohistiocytosis manifestations | |
TIM‐3 deficiency presenting with two clonally unrelated episodes of mesenteric and subcutaneous panniculitis‐like T‐cell lymphoma and hemophagocytic lymphohistiocytosis | |
Tracing the specificity of CRISPR-Cas nucleases in clinically relevant human cells | |
Transkriptionsfaktor T-bet wird durch IL-15 und Agonistenselektion induziert und kontrolliert die Entwicklung von CD8αα+ intraepithelialen Lymphozyten = Der Transkriptionsfaktor T-bet wird durch IL-15 und Agonistenselektion induziert und kontrolliert die Entwicklung von CD8[alpha][alpha]+ intraepithelialen Lymphozyten | |
Trigger‐dependent differences determine therapeutic outcome in murine primary hemophagocytic lymphohistiocytosis | |
Tuberculosis-associated HLH in an 8-month-old infant: a case report and review |