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Die folgenden Publikationen sind in der Online-Universitätsbibliographie der Universität Duisburg-Essen verzeichnet. Weitere Informationen finden Sie gegebenenfalls auch auf den persönlichen Webseiten der Person.
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Aberrant Naive CD4–Positive T Cell Differentiation in Systemic Juvenile Idiopathic Arthritis Committed to B Cell HelpIn: Arthritis & Rheumatology (2022)ISSN: 2326-5191; 2326-5205Online Volltext: dx.doi.org/ (Open Access)
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MRP8/14 serum levels as diagnostic markers for systemic juvenile idiopathic arthritis in children with prolonged feverIn: Rheumatology Jg. 61 (2022) Nr. 7, S. 3082 - 3092ISSN: 1462-0324; 1462-0332Online Volltext: dx.doi.org/
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Phenotypic spectrum in recessive STING-associated vasculopathy with onset in infancy: Four novel cases and analysis of previously reported casesIn: Frontiers in Immunology Jg. 13 (2022)ISSN: 1664-3224Online Volltext: dx.doi.org/ (Open Access)
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Prevention of disease flares by risk-adapted stratification of therapy withdrawal in juvenile idiopathic arthritis : Results from the PREVENT-JIA trialIn: Annals of the Rheumatic Diseases (ARD) Jg. 81 (2022) Nr. 7, S. 990 - 997ISSN: 0003-4967; 1468-2060Online Volltext: dx.doi.org/ (Open Access)
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Rubella vaccine–induced granulomas are a novel phenotype with incomplete penetrance of genetic defects in cytotoxicityIn: The Journal of Allergy and Clinical Immunology Jg. 149 (2022) Nr. 1, S. 388 - 399.e4ISSN: 1097-6825; 0091-6749Online Volltext: dx.doi.org/ (Open Access)
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Therapeutic options for CTLA-4 insufficiencyIn: The Journal of Allergy and Clinical Immunology Jg. 149 (2022) Nr. 2, S. 736 - 746ISSN: 1097-6825; 0091-6749Online Volltext: dx.doi.org/
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Treatment of inborn errors of immunity patients with inflammatory bowel disease phenotype by allogeneic stem cell transplantationIn: British Journal of Haematology (2022) in pressISSN: 1365-2141; 0007-1048Online Volltext: dx.doi.org/ (Open Access)
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Update of evidence- and consensus-based guidelines for the treatment of juvenile idiopathic arthritis (JIA) by the German Society of Pediatric and Juvenile Rheumatic Diseases (GKJR) : New perspectives on interdisciplinary careIn: Clinical Immunology Jg. 245 (2022)ISSN: 1521-7035; 1521-6616Online Volltext: dx.doi.org/
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Use of MRP8/14 in clinical practice as a predictor of outcome after methotrexate withdrawal in patients with juvenile idiopathic arthritisIn: Clinical Rheumatology Jg. 41 (2022) Nr. 9, S. 2825 - 2830ISSN: 0770-3198; 1434-9949Online Volltext: dx.doi.org/ (Open Access)
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6/m mit Fieber und Bauchschmerzen: Vorbereitung auf die Facharztprüfung : Fall 24In: Monatsschrift für Kinderheilkunde (2021)ISSN: 1433-0474; 0026-9298Online Volltext: dx.doi.org/
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A Retrospective Analysis of Rituximab Treatment for B Cell Depletion in Different Pediatric IndicationsIn: Frontiers in Pediatrics Jg. 9 (2021)ISSN: 2296-2360Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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A distinct CD38⁺CD45RA⁺ population of CD4⁺, CD8⁺, and double-negative T cells is controlled by FASIn: Journal of Experimental Medicine (JEM) Jg. 218 (2021) Nr. 2, S. e20192191ISSN: 1540-9538; 0022-1007Online Volltext: dx.doi.org/ (Open Access)
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Biallelic PI4KA variants cause neurological, intestinal and immunological diseaseIn: Brain: A Journal of Neurology Jg. 144 (2021) Nr. 12, S. 3597 - 3610ISSN: 0006-8950; 1460-2156Online Volltext: dx.doi.org/ (Open Access)
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Definition and validation of serum biomarkers for optimal differentiation of hyperferritinaemic cytokine storm conditions in children : a retrospective cohort studyIn: The Lancet Rheumatology Jg. 3 (2021) Nr. 8, S. e563 - e573ISSN: 2665-9913Online Volltext: dx.doi.org/ (Open Access)
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HSCT is effective in patients with PSTPIP1-associated myeloid-related proteinemia inflammatory (PAMI) syndromeIn: The Journal of Allergy and Clinical Immunology Jg. 148 (2021) Nr. 1, S. 250 - 255.e1ISSN: 1097-6825; 0091-6749Online Volltext: dx.doi.org/
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TBK1 and TNFRSF13B mutations and an autoinflammatory disease in a child with lethal COVID-19In: npj Genomic Medicine Jg. 6 (2021) Nr. 1,ISSN: 2056-7944Online Volltext: dx.doi.org/ (Open Access)
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Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutationsIn: The Journal of Allergy and Clinical Immunology Jg. 146 (2020) Nr. 4, S. 901 - 911ISSN: 1097-6825; 0091-6749Online Volltext: dx.doi.org/ (Open Access)
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Consensus protocols for the diagnosis and management of the hereditary autoinflammatory syndromes CAPS, TRAPS and MKD/HIDS : a German PRO-KIND initiativeIn: Pediatric Rheumatology Jg. 18 (2020) S. 17ISSN: 1546-0096Online Volltext: dx.doi.org/ (Open Access)
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Extended clinical and immunological phenotype and transplant outcome in CD27 and CD70 deficiencyIn: Blood Jg. 136 (2020) Nr. 23, S. 2638 - 2655ISSN: 1528-0020; 0006-4971Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Synergistic signaling of TLR and IFNα/β facilitates escape of IL-18 expression from endotoxin toleranceIn: American Journal of Respiratory and Critical Care Medicine Jg. 201 (2020) Nr. 5, S. 526 - 539ISSN: 1535-4970; 1073-449X; 0003-0805Online Volltext: dx.doi.org/ (Open Access)
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Alarmins of the S100-Family in Juvenile Autoimmune and Auto-Inflammatory DiseasesIn: Frontiers in Immunology Jg. 10 (2019) S. 182ISSN: 1664-3224Online Volltext: dx.doi.org/ (Open Access)
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Molecular signature characterisation of different inflammatory phenotypes of systemic juvenile idiopathic arthritisIn: Annals of the Rheumatic Diseases (ARD) Jg. 78 (2019) Nr. 8, S. 1107 - 1113ISSN: 0003-4967; 1468-2060Online Volltext: dx.doi.org/
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Treatment to Target Using Recombinant Interleukin-1 Receptor Antagonist as First-Line Monotherapy in New-Onset Systemic Juvenile Idiopathic Arthritis : Results From a Five-Year Follow-Up StudyIn: Arthritis & Rheumatology Jg. 71 (2019) Nr. 7, S. 1163 - 1173ISSN: 2326-5191; 2326-5205Online Volltext: dx.doi.org/ (Open Access)
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Calcium and zinc tune autoinflammatory Toll-like receptor 4 signaling by S100A12In: The Journal of Allergy and Clinical Immunology Jg. 142 (2018) Nr. 4, S. 1370 - 1373.e8ISSN: 1097-6825; 0091-6749Online Volltext: dx.doi.org/ (Open Access)
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Interleukin-18 diagnostically distinguishes and pathogenically promotes human and murine macrophage activation syndromeIn: Blood Jg. 131 (2018) Nr. 13, S. 1442 - 1455ISSN: 1528-0020; 0006-4971Online Volltext: dx.doi.org/ (Open Access)
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Panton-Valentine Leukocidin associated with S. aureus osteomyelitis activates platelets via neutrophil secretion productsIn: Scientific Reports Jg. 8 (2018) Nr. 1, S. 2185ISSN: 2045-2322Online Volltext: dx.doi.org/ (Open Access)
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Peripheral blood monocytes reveal an activated phenotype in pediatric uveitisIn: Clinical Immunology Jg. 190 (2018) S. 84 - 88ISSN: 1521-7035; 1521-6616Online Volltext: dx.doi.org/
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Practice and consensus-based strategies in diagnosing and managing systemic juvenile idiopathic arthritis in GermanyIn: Pediatric Rheumatology Jg. 16 (2018) S. 7ISSN: 1546-0096Online Volltext: dx.doi.org/ (Open Access)
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Proteomic identification of systemic-onset juvenile idiopathic arthritis phenotypic biomarkersIn: Annals of the Rheumatic Diseases (ARD) Jg. 77 (2018) Nr. Suppl. 2,ISSN: 0003-4967; 1468-2060Online Volltext: dx.doi.org/ (Open Access)
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S100A12 is associated with response to therapy in juvenile idiopathic arthritisIn: The Journal of Rheumatology Jg. 45 (2018) Nr. 4, S. 547 - 554ISSN: 1499-2752; 0315-162XOnline Volltext: dx.doi.org/ Online Volltext (Open Access)
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Serum S100 Proteins as a Marker of Disease Activity in Large Vessel VasculitisIn: Journal of Clinical Rheumatology Jg. 24 (2018) Nr. 7, S. 393 - 395ISSN: 1076-1608; 1536-7355Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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The German version of the Juvenile Arthritis Multidimensional Assessment Report (JAMAR).In: Rheumatology International Jg. 38 (2018) Nr. Suppl 1, S. 211 - 218ISSN: 1437-160XOnline Volltext: dx.doi.org/ (Open Access)
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The role of S100 proteins in the pathogenesis and monitoring of autoinflammatory diseases.In: Molecular and Cellular Pediatrics Jg. 5 (2018) S. 7ISSN: 2194-7791Online Volltext: dx.doi.org/ (Open Access)
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Consensus-based diagnostic approach to systemic juvenile idiopathic arthritis in GermanyIn: Arthritis & Rheumatology Jg. 69 (2017) Nr. Suppl. 4, S. 109 - 110ISSN: 2326-5191; 2326-5205
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Correlation of Secretory Activity of Neutrophils With Genotype in Patients With Familial Mediterranean FeverIn: Arthritis & Rheumatology Jg. 68 (2016) Nr. 12, S. 3010 - 3022ISSN: 2326-5191; 2326-5205Online Volltext: dx.doi.org/
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Neutrophil-Specific S100A12 Phenotype Correlates to Genotype in Familial Mediterranean FeverIn: Annals of the Rheumatic Diseases (ARD) Jg. 74 (2015) Nr. Suppl. 2, S. 615ISSN: 0003-4967; 1468-2060Online Volltext: dx.doi.org/
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Genetische Fiebersyndrome : Hereditäre rekurrierende (periodische) FiebersyndromeIn: Zeitschrift für Rheumatologie Jg. 72 (2013) Nr. 4, S. 332 - 338ISSN: 0340-1855; 1435-1250Online Volltext: dx.doi.org/
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Genotype-phenotype and genotype-origin correlations in children with familial mediterranean fever in GermanyIn: Zeitschrift für Rheumatologie Jg. 72 (2013) Nr. Suppl. 2, S. 93ISSN: 0340-1855; 1435-1250Online Volltext: dx.doi.org/
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Hereditäre rekurrierende Fiebersyndrome (HRF) : Subgruppe der autoinflammatorischen Erkrankungen (AID)In: Monatsschrift für Kinderheilkunde Jg. 160 (2012) Nr. 8, S. 756 - 763ISSN: 1433-0474; 0026-9298Online Volltext: dx.doi.org/
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Translational research network and patient registry for auto-inflammatory diseasesIn: Rheumatology Jg. 50 (2011) Nr. 1, S. 237 - 242ISSN: 1462-0324; 1462-0332Online Volltext: dx.doi.org/
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Klimawandel und KindergesundheitIn: Monatsschrift Kinderheilkunde Jg. 171 (2023) Nr. 2, S. 111 - 113ISSN: 0026-9298; 1433-0474Online Volltext: dx.doi.org/