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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2014 2
2015 2
2016 3
2018 3
2019 3
2020 3
2022 1
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13 results
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Must every child with long QT syndrome take a beta blocker?
Waddell-Smith KE, Earle N, Skinner JR. Waddell-Smith KE, et al. Arch Dis Child. 2015 Mar;100(3):279-82. doi: 10.1136/archdischild-2014-306864. Epub 2014 Sep 30. Arch Dis Child. 2015. PMID: 25270334 Review.
Predictors of β-blocker adherence in cardiac inherited disease.
O'Donovan CE, Waddell-Smith KE, Skinner JR, Broadbent E. O'Donovan CE, et al. Among authors: waddell smith ke. Open Heart. 2018 Dec 16;5(2):e000877. doi: 10.1136/openhrt-2018-000877. eCollection 2018. Open Heart. 2018. PMID: 30613409 Free PMC article.
Development of a cardiac inherited disease service and clinical registry: A 15-year perspective.
Earle NJ, Crawford J, Hayes I, Rees MI, French J, Stiles MK, Waddell-Smith KE, Donoghue T, Monkley R, Neas K, Aitken A, Tse R, Love DR, Skinner JR; Cardiac Inherited Diseases Group. Earle NJ, et al. Among authors: waddell smith ke. Am Heart J. 2019 Mar;209:126-130. doi: 10.1016/j.ahj.2018.11.013. Epub 2018 Dec 19. Am Heart J. 2019. PMID: 30686478 No abstract available.
Long QT Syndrome Type 1 in an Australian Indigenous Patient.
Ganesan AN, Vanoye CG, Alam F, Waddell-Smith KE, McGavigan AD, Correnti G, Haan E, Brown A, Vandenberg J, George AL Jr. Ganesan AN, et al. Among authors: waddell smith ke. Circ Genom Precis Med. 2020 Apr;13(2):e002813. doi: 10.1161/CIRCGEN.119.002813. Epub 2020 Jan 31. Circ Genom Precis Med. 2020. PMID: 32004091 Free PMC article. No abstract available.
β-Blocker Adherence in Familial Long QT Syndrome.
Waddell-Smith KE, Li J, Smith W, Crawford J, Skinner JR; Cardiac Inherited Disease Group New Zealand. Waddell-Smith KE, et al. Circ Arrhythm Electrophysiol. 2016 Aug;9(8):e003591. doi: 10.1161/CIRCEP.115.003591. Circ Arrhythm Electrophysiol. 2016. PMID: 27516460
Penetrance and expressivity of the R858H CACNA1C variant in a five-generation pedigree segregating an arrhythmogenic channelopathy.
Gardner RJM, Crozier IG, Binfield AL, Love DR, Lehnert K, Gibson K, Lintott CJ, Snell RG, Jacobsen JC, Jones PP, Waddell-Smith KE, Kennedy MA, Skinner JR. Gardner RJM, et al. Among authors: waddell smith ke. Mol Genet Genomic Med. 2019 Jan;7(1):e00476. doi: 10.1002/mgg3.476. Epub 2018 Oct 21. Mol Genet Genomic Med. 2019. PMID: 30345660 Free PMC article.
13 results