Lehrstuhl für Kinder- und Jugendmedizin


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Journal article
Book chapter / Article in edited volumes
Authored book
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Edited Volume
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Unpublished / Preprint

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Abstract

Journal

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 Neurogenic bladder function disorders in patients with meningomyelocele: S2k guidelines on diagnostics and therapy (2015) Stein R, Assion C, Beetz R, Buerst M, Cremer R, Ermert A, Goepel M, et al. Journal article, Review article Diagnosis of X-Linked Hypohidrotic Ectodermal Dysplasia by Meibography and Infrared Thermography of the Eye (2015) Kärcher T, Dietz J, Jacobi C, Berz R, Schneider H Journal article Levothyroxine Treatment of Euthyroid Children with Autoimmune Hashimoto Thyroiditis: Results of a Multicenter, Randomized, Controlled Trial (2015) Dörr HG, Bettendorf M, Binder G, Karges B, Kneppo C, Schmidt H, Voss E, et al. Journal article Deficiency of ECHS1 causes mitochondrial encephalopathy with cardiac involvement (2015) Haack TB, Jackson CB, Murayama K, Kremer LS, Schaller A, Kotzaeridou U, De Vries MC, et al. Journal article