Professur für Kinder- u. Jugendmedizin Schwerpunkt Neuropädiatrie

Bilateral posterior persistent hyperplastic primary vitreous (2017) Hohberger B, Knorr HL, Mardin CY, Trollmann R, von Marchtaler P, Gusek-Schneider G Journal article Variable White Matter Atrophy and Intellectual Development in a Family With X-linked Creatine Transporter Deficiency Despite Genotypic Homogeneity (2017) Heussinger N, Saake M, Mennecke A, Dörr HG, Trollmann R Journal article Partial homonymous hemianopia of traumatic origin after riding a high-speed amusement ride (2016) Hohberger B, Trollmann R, Rompel O, Gölitz P, Gusek-Schneider GC Journal article Diffuse Encephalopathy Associated with Isolated Cerebral Langerhans Cell Histiocytosis (2016) Rompel O, Buslei R, Hammon M, Dörr HG, Chada M, Nikkhah G, Uder M, Trollmann R Journal article Do the exome: A case of Williams-Beuren syndrome with severe epilepsy due to a truncating de novo variant in GABRA1 (2016) Popp B, Trollmann R, Büttner C, Caliebe A, Thiel C, Hüffmeier U, Reis A, Zweier C Journal article Cherry-red spot in a 13-month-old child (2016) Hohberger B, Stenger N, Trollmann R, Mardin CY, Gusek-Schneider GC Journal article, Report Cavernous sinus thrombosis as a rare cause of exophthalmos in childhood : A case report (2016) Kamawal A, Schmidt MA, Rompel O, Gusek-Schneider GC, Mardin CY, Trollmann R Journal article, Medical case study 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 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