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Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin (DSP) Truncating Variant.
Hoorntje ET, Burns C, Marsili L, Corden B, Parikh VN, Te Meerman GJ, Gray B, Adiyaman A, Bagnall RD, Barge-Schaapveld DQCM, van den Berg MP, Bootsma M, Bosman LP, Correnti G, Duflou J, Eppinga RN, Fatkin D, Fietz M, Haan E, Jongbloed JDH, Hauer AD, Lam L, van Lint FHM, Lota A, Marcelis C, McCarthy HJ, van Mil AM, Oldenburg RA, Pachter N, Planken RN, Reuter C, Semsarian C, van der Smagt JJ, Thompson T, Vohra J, Volders PGA, van Waning JI, Whiffin N, van den Wijngaard A, Amin AS, Wilde AAM, van Woerden G, Yeates L, Zentner D, Ashley EA, Wheeler MT, Ware JS, van Tintelen JP, Ingles J. Hoorntje ET, et al. Among authors: van den wijngaard a. Circ Genom Precis Med. 2023 Feb;16(1):e003672. doi: 10.1161/CIRCGEN.121.003672. Epub 2022 Dec 29. Circ Genom Precis Med. 2023. PMID: 36580316 Free PMC article. Review.
Exercise related ventricular arrhythmias are related to cardiac fibrosis in hypertrophic cardiomyopathy mutation carriers.
van Rijsingen IA, Bekkers SC, Schalla S, Hermans-van Ast JF, Snoep G, Alzand BS, Arens YH, van den Wijngaard A, Crijns HJ, Pinto YM. van Rijsingen IA, et al. Among authors: van den wijngaard a. Neth Heart J. 2011 Apr;19(4):168-174. doi: 10.1007/s12471-011-0090-8. Epub 2011 Feb 17. Neth Heart J. 2011. PMID: 21475680 Free PMC article.
Scoliosis surgery in a patient with "de novo" myosin storage myopathy.
Stalpers X, Verrips A, Braakhekke J, Lammens M, van den Wijngaard A, Mostert A. Stalpers X, et al. Among authors: van den wijngaard a. Neuromuscul Disord. 2011 Nov;21(11):812-5. doi: 10.1016/j.nmd.2011.05.005. Epub 2011 Jun 30. Neuromuscul Disord. 2011. PMID: 21723124
Biologically relevant effects of mRNA amplification on gene expression profiles.
van Haaften RI, Schroen B, Janssen BJ, van Erk A, Debets JJ, Smeets HJ, Smits JF, van den Wijngaard A, Pinto YM, Evelo CT. van Haaften RI, et al. Among authors: van erk a, van den wijngaard a. BMC Bioinformatics. 2006 Apr 11;7:200. doi: 10.1186/1471-2105-7-200. BMC Bioinformatics. 2006. PMID: 16608515 Free PMC article.
Two related Dutch families with a clinically variable presentation of cardioskeletal myopathy caused by a novel S13F mutation in the desmin gene.
Bergman JE, Veenstra-Knol HE, van Essen AJ, van Ravenswaaij CM, den Dunnen WF, van den Wijngaard A, van Tintelen JP. Bergman JE, et al. Among authors: van essen aj, den dunnen wf, van ravenswaaij cm, van den wijngaard a, van tintelen jp. Eur J Med Genet. 2007 Sep-Oct;50(5):355-66. doi: 10.1016/j.ejmg.2007.06.003. Epub 2007 Jul 15. Eur J Med Genet. 2007. PMID: 17720647
Severe cardiac phenotype with right ventricular predominance in a large cohort of patients with a single missense mutation in the DES gene.
van Tintelen JP, Van Gelder IC, Asimaki A, Suurmeijer AJ, Wiesfeld AC, Jongbloed JD, van den Wijngaard A, Kuks JB, van Spaendonck-Zwarts KY, Notermans N, Boven L, van den Heuvel F, Veenstra-Knol HE, Saffitz JE, Hofstra RM, van den Berg MP. van Tintelen JP, et al. Among authors: van spaendonck zwarts ky, van den heuvel f, van den berg mp, van gelder ic, van den wijngaard a. Heart Rhythm. 2009 Nov;6(11):1574-83. doi: 10.1016/j.hrthm.2009.07.041. Epub 2009 Jul 28. Heart Rhythm. 2009. PMID: 19879535
88 results