Prof. Dr. Regina Trollmann



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Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

Publication year

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To

Abstract

Journal

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 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 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