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Scientific Reports|January 5, 2023
Time to diagnosis of Duchenne muscular dystrophy in Austria and GermanyMiriam Hiebeler, Simone Thiele, Peter Reilich, et al.Wiener Klinische Wochenschrift|January 18, 2011
Functional electrical stimulation combined with botulinum toxin type A to improve hand function in children with spastic hemiparesis - a pilot studyKarin Pieber, Malvina Herceg, Franziska Wick, et al.Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance|September 24, 2016
Myocardial late gadolinium enhancement is associated with clinical presentation in Duchenne muscular dystrophy carriersPaul Wexberg, Marion Avanzini, Julia Mascherbauer, et al.BMJ Case Reports|June 21, 2011
Isolated cytochrome c oxidase deficiency as a cause of MELASWalter Rossmanith, Michael Freilinger, Julia Roka, et al.Der Nervenarzt|July 5, 2019
[Non-ambulatory patients with Duchenne muscular dystrophy : Recommendations for monitoring disease progression and course of treatment]Marina Flotats-Bastardas, Daniel Ebrahimi-Fakhari, Günther Bernert, et al.Neurology|September 5, 2014
Long-term follow-up in patients with CCFDN syndromeMaggie C Walter, Günther Bernert, Uta Zimmermann, et al.European Journal of Pediatrics|June 26, 2015
Intracranial hemorrhage and other symptoms in infants associated with human parechovirus in Vienna, AustriaHerbert Kurz, Ruth Prammer, Wolfgang Bock, et al.Brain : a Journal of Neurology|February 5, 2003
Mutations in the ganglioside-induced differentiation-associated protein-1 (GDAP1) gene in intermediate type autosomal recessive Charcot-Marie-Tooth neuropathyJan Senderek, Carsten Bergmann, Vincent T Ramaekers, et al.Brain : a Journal of Neurology|December 23, 2025
Treatment evolution in spinal muscular atrophy: insights from the SMArtCARE registryCornelia Voigt-Müller, Michelle Pfaffenlehner, Günther Bernert, et al.Orphanet Journal of Rare Diseases|January 23, 2019
SMArtCARE - A platform to collect real-life outcome data of patients with spinal muscular atrophyAstrid Pechmann, Kirsten König, Günther Bernert, et al.Pageof 4