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Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands.
Christiaans I, Nannenberg EA, Dooijes D, Jongbloed RJ, Michels M, Postema PG, Majoor-Krakauer D, van den Wijngaard A, Mannens MM, van Tintelen JP, van Langen IM, Wilde AA. Christiaans I, et al. Among authors: michels m. Neth Heart J. 2010 May;18(5):248-54. doi: 10.1007/BF03091771. Neth Heart J. 2010. PMID: 20505798 Free PMC article.
Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy.
van den Wijngaard A, Volders P, Van Tintelen JP, Jongbloed JD, van den Berg MP, Lekanne Deprez RH, Mannens MM, Hofmann N, Slegtenhorst M, Dooijes D, Michels M, Arens Y, Jongbloed R, Smeets BJ. van den Wijngaard A, et al. Among authors: michels m. Neth Heart J. 2011 Aug;19(7-8):344-51. doi: 10.1007/s12471-011-0135-z. Neth Heart J. 2011. PMID: 21533915 Free PMC article.
Extra energy for hearts with a genetic defect: ENERGY trial.
van Driel BO, van Rossum AC, Michels M, Huurman R, van der Velden J. van Driel BO, et al. Among authors: michels m. Neth Heart J. 2019 Apr;27(4):200-205. doi: 10.1007/s12471-019-1239-0. Neth Heart J. 2019. PMID: 30767167 Free PMC article.
433 results