T. Schwerd

发表

Metabolomic Signatures in Pediatric Crohn’s Disease Patients with Mild or Quiescent Disease Treated with Partial Enteral Nutrition: A Feasibility Study

B. Koletzko, S. Koletzko, Jair Gonzalez Marques, 2020, SLAS technology.

Anti-TNF therapy for inflammatory bowel disease in patients with neurodegenerative Niemann-Pick disease Type C [version 1; peer review: 1 approved]

H. Uhlig, F. Platt, L. Peyrin-Biroulet, 2022 .

Anti-TNF therapy for inflammatory bowel disease in patients with neurodegenerative Niemann-Pick disease Type C [version 1; peer review: awaiting peer review]

H. Uhlig, F. Platt, L. Peyrin-Biroulet, 2022 .

Variants in TRIM22 That Affect NOD2 Signaling Are Associated With Very-Early-Onset Inflammatory Bowel Disease.

Eric E Schadt, Yongzhong Zhao, Christoph Klein, 2016, Gastroenterology.

Anti-TNF therapy for inflammatory bowel disease in patients with neurodegenerative Niemann-Pick disease Type C

H. Uhlig, F. Platt, L. Peyrin-Biroulet, 2022, Wellcome open research.

Role of caspase-1 in nuclear translocation of IL-37, release of the cytokine, and IL-37 inhibition of innate immune responses

C. Dinarello, M. Nold, Claudia A. Nold-Petry, 2014, Proceedings of the National Academy of Sciences.

5′-triphosphate RNA requires base-paired structures to activate antiviral signaling via RIG-I

A. Schmidt, S. Endres, T. Schwerd, 2009, Proceedings of the National Academy of Sciences.

Autophagy-Dependent Generation of Free Fatty Acids Is Critical for Normal Neutrophil Differentiation

S. Jacobsen, H. Uhlig, A. Simon, 2017, Immunity.

Increase of Intra-abdominal Adipose Tissue in Pediatric Crohn Disease

H. Hetterich, S. Koletzko, K. Frivolt, 2017, Journal of pediatric gastroenterology and nutrition.

Epstein–Barr Virus Prevalence at Diagnosis and Seroconversion during Follow-Up in Pediatric Inflammatory Bowel Disease

S. Koletzko, Annecarin Brückner, T. Schwerd, 2021, Journal of clinical medicine.

Diet prevents the expansion of segmented filamentous bacteria and ileo-colonic inflammation in a model of Crohn’s disease

S. Zeissig, D. Haller, J. Panés, 2022, bioRxiv.

Exclusive enteral nutrition in active pediatric Crohn disease: Effects on intestinal microbiota and immune regulation.

H. Uhlig, D. Haller, G. Katona, 2016, The Journal of allergy and clinical immunology.

This information is current as by Regulatory T Cells Immunostimulatory RNA Blocks Suppression

V. Hornung, G. Hartmann, S. Endres, 2009 .

Intestinal Expression of the Anti-Inflammatory Interleukin-1 Homologue IL-37 in Pediatric Inflammatory Bowel Disease

S. Weidlich, R. Kappler, S. Koletzko, 2014, Journal of pediatric gastroenterology and nutrition.

NBAS Variants Are Associated with Quantitative and Qualitative NK and B Cell Deficiency

T. Giese, H. Prokisch, C. Klein, 2021, Journal of Clinical Immunology.

Consequences of Identifying XIAP Deficiency in an Adult Patient With Inflammatory Bowel Disease.

P. Klenerman, C. Anderson, S. Travis, 2018, Gastroenterology.

Hyperadiponectinemia During Infliximab Induction Therapy in Pediatric Crohn Disease

S. Koletzko, K. Frivolt, K. Werkstetter, 2017, Journal of pediatric gastroenterology and nutrition.

Metabolic changes during exclusive enteral nutrition in pediatric Crohn’s disease patients

B. Koletzko, S. Koletzko, T. Schwerd, 2022, Metabolomics.

A biallelic mutation in IL6ST encoding the GP130 co-receptor causes immunodeficiency and craniosynostosis

S. Holland, D. Schmidt-Arras, S. Twigg, 2017, The Journal of experimental medicine.

Immunostimulatory RNA Blocks Suppression by Regulatory T Cells

V. Hornung, G. Hartmann, S. Endres, 2009, The Journal of Immunology.

The diagnostic approach to monogenic very early onset inflammatory bowel disease.

C. Klein, S. Travis, S. Snapper, 2014, Gastroenterology.

Deficiency in X-linked inhibitor of apoptosis protein promotes susceptibility to microbial triggers of intestinal inflammation

D. Aust, J. Kelsen, C. Klein, 2021, Science Immunology.

Clinical Genomics for the Diagnosis of Monogenic Forms of Inflammatory Bowel Disease: A Position Paper From the Paediatric IBD Porto Group of European Society of Paediatric Gastroenterology, Hepatology and Nutrition

A. Griffiths, C. Klein, S. Travis, 2020, Journal of Pediatric Gastroenterology & Nutrition.

Impaired antibacterial autophagy links granulomatous intestinal inflammation in Niemann–Pick disease type C1 and XIAP deficiency with NOD2 variants in Crohn's disease

Smita Y. Patel, R. Xavier, S. Kugathasan, 2016, Gut.

Somatic mosaicism and common genetic variation contribute to the risk of very-early-onset inflammatory bowel disease

J. Danesh, M. Daly, J. Stelling, 2020, Nature Communications.

Clinical Genomics for the Diagnosis of Monogenic forms of Inflammatory Bowel Disease: A Position Paper from The Paediatric IBD Porto Group of ESPGHAN.

A. Griffiths, C. Klein, S. Travis, 2020, Journal of pediatric gastroenterology and nutrition.

A variant in IL6ST with a selective IL-11 signaling defect in human and mouse

J. Scheller, D. Schmidt-Arras, S. Rose-John, 2020, Bone Research.

Esophageal Perforation and EVAC in Pediatric Patients: A Case Series of Four Children

D. V. von Schweinitz, S. Koletzko, T. Schwerd, 2021, Frontiers in Pediatrics.

Valosin-containing protein-regulated endoplasmic reticulum stress causes NOD2-dependent inflammatory responses

C. Klein, Yue Li, S. Snapper, 2022, Scientific Reports.

From Genes to Mechanisms: The Expanding Spectrum of Monogenic Disorders Associated with Inflammatory Bowel Disease

H. Uhlig, T. Schwerd, 2016, Inflammatory bowel diseases.

Inflammatory Signaling by NOD-RIPK2 Is Inhibited by Clinically Relevant Type II Kinase Inhibitors

A. Degterev, A. Bullock, S. Ray, 2015, Chemistry & biology.

Characterization of Crohn disease in X-linked inhibitor of apoptosis-deficient male patients and female symptomatic carriers.

Smita Y. Patel, A. Fischer, J. Hugot, 2014, The Journal of allergy and clinical immunology.

5′-triphosphate-siRNA: turning gene silencing and Rig-I activation against melanoma

Svetlana Shulga Morskaya, C. Berking, M. Neuenhahn, 2008, Nature Medicine.

NOX1 loss-of-function genetic variants in patients with inflammatory bowel disease

J. Danesh, M. Parkes, J. Kelsen, 2017, Mucosal Immunology.

NOX1 loss-of-function genetic variants in patients with inflammatory bowel disease

Jimmy D Bell, J. Danesh, G. McVean, 2017, Mucosal Immunology.

Repeated exclusive enteral nutrition in the treatment of paediatric Crohn's disease: predictors of efficacy and outcome

S. Koletzko, K. Frivolt, K. Werkstetter, 2014, Alimentary pharmacology & therapeutics.

Fecal Microbiota Transplantation for Recurrent Clostridium difficile Infection and Other Conditions in Children: A Joint Position Paper From the North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition and the European Society for Pediatric Gastroenterology, Hepatology, and N

H. Szajewska, R. Shamir, T. D. de Meij, 2019, Journal of pediatric gastroenterology and nutrition.

Selective loss of function variants in IL6ST cause Hyper-IgE syndrome with distinct impairments of T-cell phenotype and function

I. Tezcan, S. Twigg, A. Wilkie, 2018, Haematologica.

Children with Localized Crohn's Disease Benefit from Early Ileocecal Resection and Perioperative Anti-Tumor Necrosis Factor Therapy

T. Schwerd, J. Hubertus, B. Häberle, 2022, European Journal of Pediatric Surgery.

Partial enteral nutrition has no benefit on bone health but improves growth in paediatric patients with quiescent or mild Crohn's disease.

B. Koletzko, O. Uhl, D. Haller, 2020, Clinical nutrition.

Following Pediatric and Adult IBD Patients through the COVID-19 Pandemic: Changes in Psychosocial Burden and Perception of Infection Risk and Harm over Time

M. Standl, A. Wieser, S. Koletzko, 2021, Journal of clinical medicine.

Loss of IL-10 signaling in macrophages limits bacterial killing driven by prostaglandin E2

Daniel J. Gaffney, G. Dougan, N. Thomson, 2019, The Journal of experimental medicine.

Is Autologous Fecal Microbiota Transfer after Exclusive Enteral Nutrition in Pediatric Crohn’s Disease Patients Rational and Feasible? Data from a Feasibility Test

D. Haller, K. Neuhaus, M. Vehreschild, 2023, Nutrients.

A recessive form of extreme macrocephaly and mild intellectual disability complements the spectrum of PTEN hamartoma tumour syndrome

H. Uhlig, R. Abou Jamra, A. Reis, 2015, European Journal of Human Genetics.

[Crohn's Disease Exclusion Diet - an alternative to exlusive enteral nutritional therapy in children and adolescents with Crohn's disease? Statement of the GPGE working groups CEDATA and Nutrition/Nutrition Medicine].

T. Schwerd, A. Schmidt-Choudhury, M. Classen, 2020, Zeitschrift fur Gastroenterologie.

Human Receptor-Interacting Serine / Threonine-Protein Kinase 2 ( RIPK 2 ) A Target Enabling Package ( TEP )

Jennifer A. Ward, S. Knapp, A. Degterev, 2020 .