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Browsing by Author Rijlaarsdam, M.E.

Full Text	Issue Date	Title	Author(s)
	2011	The clinical spectrum of complete FBN1 allele deletions.	Hilhorst-Hofstee, Y.; Hamel, B.C.J.; Verheij, J.B.G.M.; Rijlaarsdam, M.E.; Mancini, G.M., et al
	2010	A multicenter, long-term study on arrhythmias in children with Ebstein anomaly.	Delhaas, T.; Sarvaas, G.J.; Rijlaarsdam, M.E.; Strengers, J.L.; Eveleigh, R.M., et al
	2010	The Clinical Spectrum of Missense Mutations of the First Aspartic Acid of cbEGF-like Domains in Fibrillin-1, Including a Recessive Family.	Hilhorst-Hofstee, Y.; Rijlaarsdam, M.E.; Scholte, A.J.H.A.; Swart-van den Berg, M.; Versteegh, M.I., et al
	2007	Ebstein's anomaly: factors associated with death in childhood and adolescence: a multi-centre, long-term study.	Kapusta, L.; Eveleigh, R.M.; Poulino, S.E.; Rijlaarsdam, M.E.; Marchie-Sarvaas, G.J. du, et al
	2005	An unexpected cause of a recurrent cerebral hemorrhage.	Thijs, R.D.; Hazekamp, M.G.; Rijlaarsdam, M.E.; Willems, S.M.; Schutte, P.J., et al