Department of Paediatrics and Adolescent Medicine

Red blood cell omega-3 fatty acids and the risk of ventricular arrhythmias in patients with heart failure (2008) Wilhelm M, Tobias R, Asskali F, Kraehner R, Kuly S, Klinghammer L, Böhles HJ, Daniel W Journal article, Original article Cell-based resurfacing of large cartilage defects: Long-term evaluation of grafts from autologous transgene-activated periosteal cells in a porcine model of osteoarthritis (2008) Gelse K, Muehle C, Franke O, Park J, Jehle M, Durst K, Göken M, et al. Journal article Uteroplacental insufficiency after bilateral uterine artery ligation in the rat: Impact on postnatal glucose and lipid metabolism and evidence for metabolic programming of the offspring by sham operation (2008) Nüsken KD, Dötsch J, Rauh M, Rascher W, Schneider H Journal article, Original article Deficiency in the LIM-only protein FHL2 impairs assembly of extracellular matrix proteins (2008) Park JH, Will C, Martin B, Gullotti L, Friedrichs N, Büttner R, Schneider H, et al. Journal article, Original article Biological function of laminin-5 and pathogenic impact of its deficiency (2007) Schneider H, Mühle C, Pacho F Journal article, Review article Angiotensin II Type 1 Receptor Blockade Prevents Lethal Malignant Hypertension (2007) Hilgers KF, Hartner A, Porst M, Veelken R, Mann J Journal article Deficiency in the LIM-only protein Fhl2 impairs skin wound healing (2007) Wixler V, Hirner S, Müller JM, Gullotti L, Will C, Kirfel J, Günther T, et al. Journal article, Original article Functional characterization of a novel CFTR mutation P67S identified in a patient with atypical cystic fibrosis (2007) Kraus C, Reis A, Naehrlich L, Dötsch J, Korbmacher C, Rauh R Journal article, Original article Intrauterine growth after uterine artery ligation in rats: Dependence on the fetal position in the uterine horn and need for prenatal marking of the animals (2007) Nüsken KD, Warnecke C, Hilgers KF, Schneider H Journal article, Original article Recurrent inversion with concomitant deletion and insertion events in the coagulation factor VIII gene suggests a new mechanism for X-chromosomal rearrangements causing hemophilia A. (2007) Mühle C, Zenker M, Chuzhanova N, Schneider H Journal article, Original article