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Phenotypic Spectrum of HCN4 Mutations: A Clinical Case.
Servatius H, Porro A, Pless SA, Schaller A, Asatryan B, Tanner H, de Marchi SF, Roten L, Seiler J, Haeberlin A, Baldinger SH, Noti F, Lam A, Fuhrer J, Moroni A, Medeiros-Domingo A. Servatius H, et al. Among authors: pless sa. Circ Genom Precis Med. 2018 Feb;11(2):e002033. doi: 10.1161/CIRCGEN.117.002033. Circ Genom Precis Med. 2018. PMID: 29440115 Free article. No abstract available.
Unexplained cardiac arrest: a tale of conflicting interpretations of KCNQ1 genetic test results.
Chua HC, Servatius H, Asatryan B, Schaller A, Rieubland C, Noti F, Seiler J, Roten L, Baldinger SH, Tanner H, Fuhrer J, Haeberlin A, Lam A, Pless SA, Medeiros-Domingo A. Chua HC, et al. Among authors: pless sa. Clin Res Cardiol. 2018 Aug;107(8):670-678. doi: 10.1007/s00392-018-1233-3. Epub 2018 Mar 26. Clin Res Cardiol. 2018. PMID: 29582136 Free article.
Probing Backbone Hydrogen Bonds in Proteins by Amide-to-Ester Mutations.
Sereikaitė V, Jensen TMT, Bartling CRO, Jemth P, Pless SA, Strømgaard K. Sereikaitė V, et al. Among authors: pless sa. Chembiochem. 2018 Oct 18;19(20):2136-2145. doi: 10.1002/cbic.201800350. Epub 2018 Oct 1. Chembiochem. 2018. PMID: 30073762 Review.
64 results