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Prof. Dr. Regina Trollmann
List of publications:
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Professur für Kinder- u. Jugendmedizin Schwerpunkt Neuropädiatrie
Project Memberships
(3)
Publications
(128)
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Journal article
Journal article
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Book chapter / Article in edited volumes
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Authored book
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Conference contribution
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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
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