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mutation cardiomyopathy family patient hypertrophic cardiomyopathy hypertrophic heart noncompaction study disease mybpc defect relative protein analysis screening adult proband cardiol cause figure sarcomere mybpc 3 gene cardiologic death heart failure carrier hypertrophy cardiomyopathie diagnosis hcm patients eur heart j myocardium coll cardiol children failure p.arg history genet founder gchapter noncompaction cardiomyopathy echocardiography non-compaction dna analysis myh 7 mutation circulation table feature myosin mybpc 3 cardiology variant myh 7 gene criteria chain chapter phenotype j med genet swets subs service family history syndrome missense sarcomeric cardiologic family screening g ϩ/lvh subjects population hoedemaeker septal function result prognosis testing factor muscle disorder family studies myh 7 mutations .2373dupg sarcomere genes
7 Most Recent Publications
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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
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Mutations in SMAD3 cause a syndromic form of aortic aneurysms and dissections with early-onset osteoarthritis
(Article)
Laar, I.M.B.H. van de Oldenburg, R. Vriend, G. Pattynama, P.M.T. Collee, J.M. Majoor-Krakauer, D.F. Poldermans, D. Frohn-Mulder, I.M.E. Micha, D. Timmermans, J. Hilhorst-Hofstee, Y. Bierma-Zeinstra, S.M.A. Pals, G. Willems, P.J. Kros, J.M. Oei, E.H.G. Oostra, B.A. Wessels, M.W. Bertoli Avella, A.M. Roos-Hesselink, J.W. Graaf, B.M. de Verhagen, J.M.A. Hoedemaekers, Y.M. Willemsen, R. Severijnen, L.A. Venselaar, H. |
2011-02-01
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Genetic Aspects and Family Studies of Noncompaction and Hypertrophic Cardiomyopathy
(Doctoral Thesis)
Hoedemaekers, Y.M. |
2010-06-25
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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
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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
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Diastolic Abnormalities as the First Feature of Hypertrophic Cardiomyopathy in Dutch Myosin-Binding Protein C Founder Mutations
(Article)
Michels, M. Soliman, O.I.I. Kofflard, M.J.M. Hoedemaekers, Y.M. Dooijes, D. Majoor-Krakauer, D.F. Cate, F.J. ten |
2009-01-01
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Cardiac β-myosin heavy chain defects in two families with non-compaction cardiomyopathy: Linking non-compaction to hypertrophic, restrictive, and dilated cardiomyopathies
(Article)
Hoedemaekers, Y.M. Caliskan, K. Majoor-Krakauer, D.F. Laar, I.M.B.H. van de Michels, M. Witsenburg, M. Cate, F.J. ten Simoons, M.L. Dooijes, D. |
2007-11-01
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