Professur für Kinder- u. Jugendmedizin Schwerpunkt Neuropädiatrie

Manipulation of medicinal products for oral administration to paediatric patients at a german university hospital: An observational study (2020) Zahn J, Hörning A, Trollmann R, Rascher W, Neubert A Journal article Dual-source computed tomography of the lung with spectral shaping and advanced iterative reconstruction: potential for maximum radiation dose reduction (2020) Wetzl M, May M, Weinmann D, Hammon M, Treutlein C, Zeilinger M, Kiefer A, et al. Journal article Diagnosis and treatment of Guillain-Barré Syndrome in childhood and adolescence: An evidence- and consensus-based guideline (2020) Korinthenberg R, Trollmann R, Felderhoff-Müser U, Bernert G, Hackenberg A, Hufnagel M, Pohl M, et al. Journal article, Review article Fatigue and depression predict health-related quality of life in patients with pediatric-onset multiple sclerosis (2019) Gravesande KSV, Blaschek A, Calabrese P, Rostasy K, Huppke P, Kessler JJ, Kalbe E, et al. Journal article Comparative Socioeconomic Study Of Patients In Germany With Dravet Syndrome, Refractory Epilepsy Or Epilepsy In Seizure Remission, And Their Caregivers (2019) Strzelczyk A, Schubert-Bast S, Bast T, Bettendorf U, Hamer H, Herting A, Kalski M, et al. Conference contribution Delineation of the clinical phenotype caused by de novo CLTC variants (2019) Sa MJN, Venselaar H, Wiel L, Trimouille A, Lasseaux E, Naudion S, Lacombe D, et al. Conference contribution Clinical characteristics, resource utilization, quality of life and care situation for patients with Dravet syndrome in Germany (2019) Kalski M, Schubert-Bast S, Kieslich M, Leyer AC, Polster T, Herting A, Mayer T, et al. Journal article Development and Usability Analysis of a Multimedia eConsent Solution (2019) Schneiderheinze H, Prokosch HU, Apel H, Bellut L, Wullich B, Trollmann R, Schüttler C Book chapter / Article in edited volumes Seizure management and prescription patterns of anticonvulsants in Dravet syndrome: A multicenter cohort study from Germany and review of literature (2019) Schubert-Bast S, Wolff M, Wiemer-Kruel A, von Spiczak S, Trollmann R, Reif PS, Pritchard C, et al. Journal article Brittle-Cornea-Syndrom Typ 1 durch Compound-Heterozygotie zweier Mutationen im ZNF469-Gen (2019) Menzel-Severing J, Meiller R, Kraus C, Trollmann R, Atalay D Journal article