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2013 1
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Page 1
Cardiac ryanodine receptor calcium release deficiency syndrome.
Sun B, Yao J, Ni M, Wei J, Zhong X, Guo W, Zhang L, Wang R, Belke D, Chen YX, Lieve KVV, Broendberg AK, Roston TM, Blankoff I, Kammeraad JA, von Alvensleben JC, Lazarte J, Vallmitjana A, Bohne LJ, Rose RA, Benitez R, Hove-Madsen L, Napolitano C, Hegele RA, Fill M, Sanatani S, Wilde AAM, Roberts JD, Priori SG, Jensen HK, Chen SRW. Sun B, et al. Among authors: roston tm. Sci Transl Med. 2021 Feb 3;13(579):eaba7287. doi: 10.1126/scitranslmed.aba7287. Sci Transl Med. 2021. PMID: 33536282 Free article.
RYR2-ryanodinopathies: from calcium overload to calcium deficiency.
Steinberg C, Roston TM, van der Werf C, Sanatani S, Chen SRW, Wilde AAM, Krahn AD. Steinberg C, et al. Among authors: roston tm. Europace. 2023 Jun 2;25(6):euad156. doi: 10.1093/europace/euad156. Europace. 2023. PMID: 37387319 Free PMC article.
Genetic testing in monogenic early-onset atrial fibrillation.
Chalazan B, Freeth E, Mohajeri A, Ramanathan K, Bennett M, Walia J, Halperin L, Roston T, Lazarte J, Hegele RA, Lehman A, Laksman Z. Chalazan B, et al. Among authors: roston t. Eur J Hum Genet. 2023 Jul;31(7):769-775. doi: 10.1038/s41431-023-01383-z. Epub 2023 May 22. Eur J Hum Genet. 2023. PMID: 37217627
Increased Ca2+ Transient Underlies RyR2-Related Left Ventricular Noncompaction.
Ni M, Li Y, Wei J, Song Z, Wang H, Yao J, Chen YX, Belke D, Estillore JP, Wang R, Vallmitjana A, Benitez R, Hove-Madsen L, Feng W, Chen J, Roston TM, Sanatani S, Lehman A, Chen SRW. Ni M, et al. Among authors: roston tm. Circ Res. 2023 Jul 7;133(2):177-192. doi: 10.1161/CIRCRESAHA.123.322504. Epub 2023 Jun 16. Circ Res. 2023. PMID: 37325910
69 results