Professur für Kinder- u. Jugendmedizin Schwerpunkt Neuropädiatrie

A multicenter, matched case-control analysis comparing burden-of-illness in Dravet syndrome to refractory epilepsy and seizure remission in patients and caregivers in Germany (2019) Strzelczyk A, Schubert-Bast S, Bast T, Bettendorf U, Fiedler B, Hamer H, Herting A, et al. Journal article Burden-of-illness and cost-driving factors in Dravet syndrome patients and carers: A prospective, multicenter study from Germany (2019) Strzelczyk A, Kalski M, Bast T, Wiemer-Kruel A, Bettendorf U, Kay L, Kieslich M, et al. Journal article SOCIO-ECONOMIC IMPACT OF DRAVET SYNDROME IN GERMANY: A REAL-WORLD STUDY (2018) Irwin J, Strzelczyk A, Kalski M, Bast T, Wiemer-Kruel A, Bettendorf U, Kieslich M, et al. Conference contribution TSC-associated neuropsychiatric disorders (TAND): findings from the TOSCA natural history study (2018) De Vries PJ, Belousova E, Benedik MP, Carter T, Cottin V, Curatolo P, Dahlin M, et al. Journal article Effects of Levetiracetam and Sulthiame on EEG in benign epilepsy with centrotemporal spikes: A randomized controlled trial (2018) Tacke M, Borggraefe I, Gerstl L, Heinen F, Vill K, Bonfert M, Bast T, et al. Journal article Compound heterozygous RYR1 mutations in a preterm with arthrogryposis multiplex congenita and prenatal CNS bleeding (2018) Brackmann F, Türk M, Gratzki N, Rompel O, Jungbluth H, Schröder R, Trollmann R Journal article A multidisciplinary systematic review of the treatment for chronic idiopathic tinnitus (2017) Zenner HP, Delb W, Kroener-Herwig B, Jaeger B, Peroz I, Hesse G, Mazurek B, et al. Journal article Rare Variant of GM2 Gangliosidosis through Activator-Protein Deficiency (2017) Brackmann F, Kehrer C, Kustermann W, Boehringer J, Kraegeloh-Mann I, Trollmann R Journal article Oxygen-sensitive regulation and neuroprotective effects of growth hormone-dependent growth factors during early postnatal development (2017) Jung S, Boie G, Dörr HG, Trollmann R Journal article Histopathological proof of the pathogenicity of a rare GFAP mutation in a patient with flaccid paraparesis (2017) Brackmann F, Coras R, Rössler K, Kraus C, Rompel O, Trollmann R Journal article