Lehrstuhl für Kinder- und Jugendmedizin

Alpha8 Integrin (Itga8) Signalling Attenuates Chronic Renal Interstitial Fibrosis by Reducing Fibroblast Activation, Not by Interfering with Regulation of Cell Turnover (2016) Marek I, Lichtneger TS, Cordasic N, Hilgers KF, Volkert G, Fahlbusch F, Rascher W, et al. Journal article GENETICS IN ENDOCRINOLOGY: Gain and loss of function mutations of the calcium-sensing receptor and associated proteins: current treatment concepts (2016) Mayr B, Schnabel D, Dörr HG, Schöfl C Journal article Genotype, Clinical Course, and Therapeutic Decision Making in 76 Infants with Severe Generalized Junctional Epidermolysis Bullosa (2016) Hammersen J, Has C, Naumann-Bartsch N, Stachel D, Kiritsi D, Söder S, Tardieu M, et al. Journal article A novel missense mutation in the gene EDARADD associated with an unusual phenotype of hypohidrotic ectodermal dysplasia (2016) Wohlfart S, Söder S, Smahi A, Schneider H Journal article Hyperactive mTOR pathway promotes lymphoproliferation and abnormal differentiation in autoimmune lymphoproliferative syndrome (2016) Voelkl S, Rensing-Ehl A, Allgäuer A, Schreiner E, Lorenz MR, Rohr J, Klemann C, et al. Journal article Adamantinomatous and papillary craniopharyngiomas are characterized by distinct epigenomic as well as mutational and transcriptomic profiles (2016) Hoelsken A, Sill M, Merkle J, Schweizer L, Buchfelder M, Flitsch J, Fahlbusch R, et al. Journal article Strong hypoxia reduces leptin synthesis in purified primary human trophoblasts (2015) Nuesken E, Herrmann Y, Wohlfarth M, Goecke TW, Appel S, Schneider H, Doetsch J, Nuesken KD Journal article A New Mouse Model of Junctional Epidermolysis Bullosa: The LAMB3 628G > A Knockin Mouse (2015) Hammersen J, Hou J, Wünsche S, Brenner S, Winkler T, Schneider H Journal article, Original article DYNC2LI1 mutations broaden the clinical spectrum of dynein-2 defects (2015) Keßler K, Wunderlich I, Uebe S, Falk N, Gießl A, Brandstätter JH, Popp B, et al. Journal article Oligoclonal bands predict multiple sclerosis in children with optic neuritis (2015) Heussinger N, Kontopantelis E, Gburek-Augustat J, Jenke A, Vollrath G, Korinthenberg R, Hofstetter P, et al. Journal article