von Anna Schaffeld ; Sietse Marten Aukema ; Claris Nde ; Chiara Vey ; Gregor Dombrowsky ; Jiao Wang ; Nico Melnik ; Matthias Freund ; Eyby Leon ; Laura Mittelstädt ; Ann-Kathrin Bauer ; Robert B Russell ; Irene E Zohn ; Marc-Phillip Hitz
Syndromtag 2025 der Deutschen Gesellschaft für Humangenetik e.V. vom 12.–13. September 2025, Essen Berlin : Deutsche Gesellschaft für Humangenetik e.V., 2025 (2025) 1 Online-Ressource
Treatment of adults by pediatric cardiologists : correspondence: Late complication after surgical treatment of aortic isthmus stenosis by Michael Huber, Dr. med. Matthias Wolf, and Prof. Dr. med. Harald Dormann in issue 5/2019
von Matthias Freund ; Reinald Motz ; Kay Kronberg ; Paul Hacke
von Rinske J IJsselhof ; Saniyé D. R. Duchateau ; Rianne M. Schouten ; Matthias Freund ; Jörg Heuser ; Zina Fejzic ; Felix Haas ; Paul H. Schoof ; Martijn G. Slieker
von Sven Dittrich ; Joseph George Pattathu ; Friedrich Ebinger ; Joachim Eichhorn ; Reinald Motz ; Christoph Korenke ; Matthias Freund ; Michael Schumacher
X-linked Duchenne muscular dystrophy (DMD), the most frequent human hereditary skeletal muscle myopathy, inevitably leads to progressive dilated cardiomyopathy. We assessed the effect and safety of a combined treatment with the ACE-inhibitor enalapril and the β-blocker metoprolol in a German cohort of infantile and juvenile DMD patients with preserved left ventricular function.
Orphanet journal of rare diseases London : BioMed Central, 2006 14(2019), Artikel-ID 105, Seite 1-13 Online-Ressource