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scopus: 16318963800

Michels, M.

(Michelle Michels)


patient hypertrophic cardiomyopathy mutation hypertrophic cardiomyopathy mybpc hcm patients study protein 11. 14. 15. 20. 16. 19. 12. 17. 10. 13. 18. 23. 24. 28. 26. 25. 27. 21. 22. 30. 29. 33. 31. 32. 34. 35. carrier 36. 38. 39. 37. septal heart chapter family diastolic subject analysis disease myectomy velocity cate fj cmybp-c donor figure untwisting mybpc 3mut founder alcohol septal ablation systolic population group cardiol effect .2864_2865delct hypertrophy death dysfunction circulation table mybpc 3 gene .2373dupg echocardiography thickness phosphorylation peak systolic twist pressure function follow-up coll cardiol force




10 Most Recent Publications

Diastolic abnormalities in normal phenotype hypertrophic cardiomyopathy gene carriers: A study using speckle tracking echocardiography (Article)
Kauer, F. Dalen, B.M. van Michels, M. Soliman, O.I.I. Vletter, W.B. Slegtenhorst, M. van Cate, F.J. ten Geleijnse, M.L.
2013-05-01
Mortality risk of untreated myosin-binding protein crelated hypertrophic cardiomyopathy: Insight into the natural history (Article)
Nannenberg, E.A. Michels, M. Langen, I.M. van Wilde, A.A.M. Sijbrands, E.J.G. Christiaans, I. Majoor-Krakauer, D.F. Hoedemaekers, Y.M. Tintelen, J.P. van Lombardi, M.P. Cate, F.J. ten Schinkel, A.F. Tijssen, J.G.P.
2011-11-29
Recurrent and founder mutations in the Netherlands: Cardiac troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy (Article)
Wijngaard, A. van den Volders, P.G.A. Michels, M. Arens, Y.H.J.M. Smeets, B.J.M. Tintelen, J.P. van Jongbloed, J.D.H. Berg, M.P. van den Lekanne Deprez, R.H. Mannens, M.M.A.M. Hofmann, N. Slegtenhorst, M. Dooijes, D.
2011-10-05
Manifest disease, risk factors for sudden cardiac death, and cardiac events in a large nationwide cohort of predictively tested hypertrophic cardiomyopathy mutation carriers: Determining the best cardiological screening strategy (Article)
Christiaans, I. Birnie, E. Arens, Y.H.J.M. DenWijngaard, A. van Atsma, D.E. Helderman-van den Enden, A.T.J.M. Houweling, A.C. Boer, K. de Smagt, J.J. van der Hauer, R.N.W. Marcelis, C. Timmermans, J. Bonsel, G.J. Langen, I.M. van Wilde, A.A.M. Mannens, M.M.A.M. Michels, M. Majoor-Krakauer, D.F. Dooijes, D. Tintelen, J.P. van Berg, M.P. van den Volders, P.G.A.
2011-05-01
Hypertrophic Cardiomyopathy: Pathophysiology, Genetics and Invasive Treatment (Doctoral Thesis)
Michels, M.
2011-01-14
The importance of genetic counseling, DNA diagnostics, and cardiologic family screening in left ventricular noncompaction cardiomyopathy (Article)
Hoedemaekers, Y.M. Caliskan, K. Michels, M. Frohn-Mulder, I.M.E. Smagt, J.J. van der Phefferkorn, J.E. Wessels, M.W. Cate, F.J. ten Sijbrands, E.J.G. Majoor-Krakauer, D.F.
2010-06-01
Long-term outcome of alcohol septal ablation in patients with obstructive hypertrophic cardiomyopathy: A word of caution (Article)
Cate, F.J. ten Soliman, O.I.I. Michels, M. Theuns, D.A.M.J. Jong, P.L. de Geleijnse, M.L. Serruys, P.W.J.C.
2010-05-01
Delayed Left Ventricular Untwisting in Hypertrophic Cardiomyopathy (Article)
Dalen, B.M. van Kauer, F. Michels, M. Soliman, O.I.I. Vletter, W.B. Zwaan, H.B. van der Cate, F.J. ten Geleijnse, M.L.
2009-12-01
Disease penetrance and risk stratification for sudden cardiac death in asymptomatic hypertrophic cardiomyopathy mutation carriers (Article)
Michels, M. Soliman, O.I.I. Phefferkorn, J.E. Hoedemaekers, Y.M. Kofflard, M.J.M. Dooijes, D. Majoor-Krakauer, D.F. Cate, F.J. ten
2009-11-01
Influence of the pattern of hypertrophy on left ventricular twist in hypertrophic cardiomyopathy (Article)
Dalen, B.M. van Kauer, F. Soliman, O.I.I. Vletter, W.B. Michels, M. Cate, F.J. ten Geleijnse, M.L.
2009-04-01