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International Journal of Colorectal Disease|May 6, 2014
PTGER4 modulating variants in Crohn's diseaseMatthias Prager, Janine Büttner, Carsten Büning
Archives of Gynecology and Obstetrics|April 22, 2009
Clinical features of hemolysis, elevated liver enzymes, and low platelet count syndrome in undiagnosed Wilson disease: report of two casesAnna Członkowska, Grażyna Gromadzka, Janine Büttner, et al.
Inflammatory Bowel Diseases|September 7, 2016
A Promoter Variant Within the Aryl Hydrocarbon Receptor Gene Is Associated with an Epithelial Barrier Defect in Smokers with Crohn's DiseaseMatthias Prager, Janine Büttner, Philip Grunert, et al.
Frontiers in Medicine|February 18, 2026
Intestinal permeability correlated with chronic fatigue in a patient with long COVID-A case report and overview of the literatureIngo Andus, Janine Büttner, Bettina Bochow-Fitzner, et al.
Obesity Surgery|March 24, 2019
Impact of Laparoscopic Sleeve Gastrectomy on Gut Permeability in Morbidly Obese SubjectsTeresa Kellerer, Beate Brandl, Janine Büttner, et al.
Journal of Human Genetics|May 17, 2008
Mutational analysis of ATP7B gene in Egyptian children with Wilson disease: 12 novel mutationsTawhida Y Abdelghaffar, Solaf M Elsayed, Ezzat Elsobky, et al.
International Journal of Colorectal Disease|November 9, 2011
The JAK2 variant rs10758669 in Crohn's disease: altering the intestinal barrier as one mechanism of actionMatthias Prager, Janine Büttner, Verena Haas, et al.
Inflammatory Bowel Diseases|February 21, 2012
Increased small intestinal permeability in ulcerative colitis: rather genetic than environmental and a risk factor for extensive disease?Carsten Büning, Nora Geissler, Matthias Prager, et al.
Nutrients|October 14, 2023
Predictive Potential of Biomarkers of Intestinal Barrier Function for Therapeutic Management with Teduglutide in Patients with Short Bowel SyndromeJanine Büttner, Elisabeth Blüthner, Sophie Greif, et al.
The Journal of Molecular Diagnostics : JMD|March 28, 2009
Hereditary apolipoprotein AI-associated amyloidosis in surgical pathology specimens: identification of three novel mutations in the APOA1 geneMagdalena Eriksson, Stefan Schönland, Saniye Yumlu, et al.
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