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Unpublished / Preprint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

From
To

Abstract

Journal

23Na MRI Depicts Early Changes in Ion Homeostasis in Skeletal Muscle Tissue of Patients With Duchenne Muscular Dystrophy (2019) Gerhalter T, Gast L, Marty B, Martin J, Trollmann R, Schüssler S, Roemer F, et al. Journal article C1 Esterase Inhibitor Reduces BBB Leakage and Apoptosis in the Hypoxic Developing Mouse Brain (2019) Jung S, Topf HG, Boie G, Trollmann R Journal article Myelin Oligodendrocyte Glycoprotein Antibody-Associated Neuromyelitis Optica Spectrum Disorder in a 6-Year-Old Boy (2019) Kamawal A, Hörning S, Galiano M, Rompel O, Trollmann R Journal article 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 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