Universitätsklinikum Köln

Hospital


Location: Köln (Cologne), Germany (DE) DE

ISNI: 000000008852305X

ROR: https://ror.org/05mxhda18

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Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

Publication year

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To

Abstract

Journal

Tyrosinase reduces expression of vascular endothelial growth factors and improves corneal graft survival (2022) Clahsen T, Hatami N, Büttner C, Reis A, Cursiefen C Conference contribution Effect of sCD83 on direct allosensitization after corneal transplantation (2022) Schoenberg AP, Peckert-Maier K, Hadrian K, Hamdorf M, Cursiefen C, Zinser E, Bock F Conference contribution RHABDOID TUMOR PREDISPOSITION SYNDROME (RTPS) - FINDING EVIDENCE BY SYSTEMATIC ANALYSES (2022) Nemes K, Bens S, Johann PD, Steinbuegl M, Gruhle M, Kachanov D, Teleshova M, et al. Conference contribution INFANTS AND NEWBORNS WITH ATYPICAL TERATOID/RHABDOID TUMORS (ATRT) AND EXTRACRANIAL MALIGNANT RHABDOID TUMORS: A UNIQUE AND CHALLENGING POPULATION (2022) Nemes K, Johann PD, Steinbuegl M, Gruhle M, Bens S, Kachanov D, Teleshova M, et al. Conference contribution Evidence-Based and Structured Diagnosis in Breast MRI using the Kaiser Score (2022) Baltzer PAT, Krug KB, Dietzel M Journal article Twenty years of newborn screening for congenital adrenal hyperplasia and congenital primary hypothyroidism - experiences from the DGKED/AQUAPE study group for quality improvement in Germany (2022) Hammersen J, Bettendorf M, Bonfig W, Schoenau E, Warncke K, Eckert AJ, Fricke-Otto S, et al. Journal article Investigation of daily Activity, Sleep and neurocognitive Function in Glioblastoma Patients using TTFields Therapy in Routine clinical Care in Germany - the TIGER PRO-Active Study (2022) Glas M, Tabatabai G, Fietkau R, Goldbrunner R, Baehr O Conference contribution Infants and Newborns with Atypical Teratoid Rhabdoid Tumors (ATRT) and Extracranial Malignant Rhabdoid Tumors (eMRT) in the EU-RHAB Registry: A Unique and Challenging Population (2022) Nemes K, Johann PD, Steinbügl M, Gruhle M, Bens S, Kachanov D, Teleshova M, et al. Journal article Alport syndrome and autosomal dominant tubulointerstitial kidney disease frequently underlie end-stage renal disease of unknown origin-a single-center analysis (2022) Leenen E, Erger F, Altmuller J, Wenzel A, Thiele H, Harth A, Tschernoster N, et al. Journal article First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1B (2022) Gehlen J, Giel AS, Köllges R, Haas SL, Zhang R, Trcka J, Sungur A, et al. Journal article