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Anzahl der Publikationen: 9
Zeitschriftenartikel
Brand, S.; Schmucker, U.; Lob, G.; Haasper, C.; Juhra, C.; Hell, W.; Rieth, P. und Matthes, G.
(2017):
Warum wieder mehr Menschen im Straßenverkehr sterben – Trendwende oder Ausreißer?
In: Zentralblatt für Chirurgie, Bd. 142, Nr. 2: S. 209-215
Stallhofer, J.; Denk, G. U.; Glas, J.; Laubender, Rüdiger P.; Göke, Burkhard; Rust, C.; Brand, S. und Pusl, T.
(2011):
Analysis of IL2/IL21 Gene Variants in Cholestatic Liver Diseases Reveals an Association with Primary Sclerosing Cholangitis.
In: Digestion, Bd. 84, Nr. 1: S. 29-35
Zitzmann, K.; de Toni, E.; Ruden, J. von; Brand, S.; Göke, Burkhard; Laubender, Rüdiger P. und Auernhammer, C. J.
(2011):
The novel Raf inhibitor Raf265 decreases Bcl-2 levels and confers TRAIL-sensitivity to neuroendocrine tumour cells.
In: Endocrine-Related Cancer, Bd. 18, Nr. 2: S. 277-285
Schroepf, S.; Kappler, R.; Brand, S.; Prell, C.; Lohse, P.; Glas, J.; Hoster, Eva; Helmbrecht, J.; Ballauff, A.; Berger, M.; Schweinitz, D. von; Koletzko, Sibylle und Lacher, M.
(2010):
Strong overexpression of CXCR3 axis components in childhood inflammatory bowel disease.
In: Inflammatory Bowel Diseases, Bd. 16, Nr. 11: S. 1882-1890
Jürgens, Matthias; Brand, S.; Laubender, Rüdiger P.; Seiderer, Julia; Glas, Jürgen; Wetzke, M.; Wagner, J.; Pfennig, S.; Tillack, C.; Beigel, Florian; Weidinger, M.; Schnitzler, Fabian; Kreis, M. E.; Göke, Burkhard; Lohse, P.; Herrmann, K. und Ochsenkühn, Thomas
(2010):
The presence of fistulas and NOD2 homozygosity strongly predict intestinal stenosis in Crohn’s disease independent of the IL23R genotype.
In: Journal of Gastroenterology, Bd. 45, Nr. 7: S. 721-731
Brand, S. und Crispin, Alexander
(2007):
C-reactive protein polymorphism and Crohn’s disease: authors’ reply.
In: Alimentary Pharmacology & Therapeutics, Bd. 25, Nr. 4: S. 520-521
Thalmaier, D.; Dambacher, J.; Seiderer, Julia; Konrad, A.; Schachinger, V.; Pfennig, S.; Otte, J. M.; Crispin, Alexander; Göke, Burkhard; Ochsenkühn, Thomas; Lohse, P. und Brand, S.
(2006):
The +1059G/C polymorphism in the C-reactive protein (CRP) gene is associated with involvement of the terminal ileum and decreased serum CRP levels in patients with Crohn’s disease.
In: Alimentary Pharmacology & Therapeutics, Bd. 24, Nr. 7: S. 1105-1115
Seiderer, Julia; Brand, S.; Herrmann, Karin A.; Schnitzler, Fabian; Hatz, R.; Crispin, Alexander; Pfennig, S.; Schoenberg, S. O.; Göke, Burkhard; Lohse, P. und Ochsenkühn, Thomas
(2006):
Predictive Value of the CARD15 Variant 1007fs for the Diagnosis of Intestinal Stenoses and the Need for Surgery in Crohn’s Disease in Clinical Practice: Results of a Prospective Study.
In: Inflammatory Bowel Diseases, Bd. 12, Nr. 12: S. 1114-1121
Brand, S.; Staudinger, T.; Schnitzler, Fabian; Pfennig, S.; Hofbauer, K.; Dambacher, J.; Seiderer, Julia; Tillack, C.; Konrad, A.; Crispin, Alexander; Göke, Burkhard; Lohse, P. und Ochsenkühn, Thomas
(2005):
The role of Toll-like receptor 4 Asp299Gly and Thr399Ile polymorphisms and CARD15/NOD2 mutations in the susceptibility and phenotype of Crohn’s disease.
In: Inflammatory Bowel Diseases, Bd. 11, Nr. 7: S. 645-652