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WITHDRAWN: Novel Xp21.1 deletion associated with unusual features in a large McLeod syndrome kindred.
Sveinsson O, Udd B, Svenningsson P, Gassner C, Engström C, Laffita-Mesa JM, Solders G, Hertegård S, Savitcheva I, Jung HH, Tolnay M, Frey BM, Paucar M. Sveinsson O, et al. Among authors: gassner c. Parkinsonism Relat Disord. 2018 Oct 8:S1353-8020(18)30399-7. doi: 10.1016/j.parkreldis.2018.09.014. Online ahead of print. Parkinsonism Relat Disord. 2018. PMID: 30305234 No abstract available.
Involuntary movements, vocalizations and cognitive decline.
Sveinsson O, Udd B, Svenningsson P, Gassner C, Engström C, Laffita-Mesa J, Solders G, Hertegård S, Savitcheva I, Jung HH, Tolnay M, Frey BM, Paucar M. Sveinsson O, et al. Among authors: gassner c. Parkinsonism Relat Disord. 2020 Oct;79:135-137. doi: 10.1016/j.parkreldis.2019.05.029. Epub 2019 May 29. Parkinsonism Relat Disord. 2020. PMID: 31153763 No abstract available.
High-throughput Kell, Kidd, and Duffy matrix-assisted laser desorption/ionization, time-of-flight mass spectrometry-based blood group genotyping of 4000 donors shows close to full concordance with serotyping and detects new alleles.
Meyer S, Vollmert C, Trost N, Brönnimann C, Gottschalk J, Buser A, Frey BM, Gassner C. Meyer S, et al. Among authors: gassner c. Transfusion. 2014 Dec;54(12):3198-207. doi: 10.1111/trf.12715. Epub 2014 May 21. Transfusion. 2014. PMID: 24845979 Clinical Trial.
134 results