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Phenotypic Diversity Caused by the DES Missense Mutation p.R127P (c.380G>C) Contributing to Significant Cardiac Mortality and Morbidity Associated With a Desmin Filament Assembly Defect.
Ebrahim MA, Ali NM, Albash BY, Al Sayegh AH, Ahmad NB, Voß S, Klag F, Groß J, Holler S, Walhorn V, Anselmetti D, Milting H, Brodehl A. Ebrahim MA, et al. Among authors: voss s. Circ Genom Precis Med. 2025 Jun;18(3):e004896. doi: 10.1161/CIRCGEN.124.004896. Epub 2025 Apr 23. Circ Genom Precis Med. 2025. PMID: 40265264
Cardiomyopathy-Associated Mutations in a Hotspot Region at the C-Terminal Part of Desmin Coil-2 Domain Impair the Intermediate Filament Assembly.
Reckmann J, Milting H, Voß S, Radukic MT, Klag F, Flottmann F, Lütkemeyer A, Groß J, Gärtner A, Landwehr S, Anselmetti D, Hoyer A, Müller KM, Gummert J, Walhorn V, Brodehl A. Reckmann J, et al. Among authors: voss s. Circ Genom Precis Med. 2026 Aug;19(4):e005653. doi: 10.1161/CIRCGEN.125.005653. Epub 2026 Jul 1. Circ Genom Precis Med. 2026. PMID: 42381621
Cephalic Vein Cutdown Is Superior to Subclavian Puncture as Venous Access for Patients with Cardiac Implantable Devices after Long-Term Follow-Up.
Knorr D, Bandorski D, Bogossian H, Iliodromitis K, Schiedat F, Karosiene Z, Mijic D, Lemke B, Seyfarth M, Voß S, Knippschild S, Aweimer A, Zarse M, Kloppe A, Botsios S. Knorr D, et al. Among authors: voss s. J Clin Med. 2024 Feb 12;13(4):1044. doi: 10.3390/jcm13041044. J Clin Med. 2024. PMID: 38398357 Free PMC article.
17 results