Publications by authors named "Ingrid M E Frohn-Mulder"

14Publications

Delayed Diagnosis of Danon Disease in Patients Presenting With Isolated Cardiomyopathy.

Circ Genom Precis Med 2019 03;12(3):e002395

Department of Clinical Genetics (S.D., M.A. v. S, M.L., M.W.W., G.J.S.), Sophia Children's Hospital, Erasmus Medical Centre, Erasmus University, Rotterdam, the Netherlands.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1161/CIRCGEN.118.002395DOI Listing
March 2019

Homozygous Truncating Variant in PKP2 Causes Hypoplastic Left Heart Syndrome.

Circ Genom Precis Med 2018 12;11(12):e002397

Department of Clinical Genetics, Erasmus MC, University Medical Center Rotterdam, Rotterdam, the Netherlands (J.M.A.V., M.v.d.B., S.K., I.M.B.H.v.d.L., M.A.v.S., M.W.W.).

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1161/CIRCGEN.118.002397DOI Listing
December 2018

Linking the heart and the brain: Neurodevelopmental disorders in patients with catecholaminergic polymorphic ventricular tachycardia.

Heart Rhythm 2019 02 28;16(2):220-228. Epub 2018 Aug 28.

AMC Heart Center, Department of Clinical and Experimental Cardiology, Academic Medical Center, Amsterdam, The Netherlands; Princess Al-Jawhara Al-Brahim Centre of Excellence in Research of Hereditary Disorders, Jeddah, Kingdom of Saudi Arabia. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.hrthm.2018.08.025DOI Listing
February 2019

Outcomes of Contemporary Family Screening in Hypertrophic Cardiomyopathy.

Circ Genom Precis Med 2018 04;11(4):e001896

Department of Cardiology, Thoraxcenter (H.G.v.V., A.F.L.S., S.J.B., M.M.), Department of Clinical Genetics (R.A.O., M.A.v.S.), and Department of Pediatrics (I.M.E.F.-M.), Erasmus Medical Center, Rotterdam, The Netherlands.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1161/CIRCGEN.117.001896DOI Listing
April 2018

Endocarditis of a congenital coronary fistula in a child.

Cardiol Young 2018 Feb 11;28(2):334-337. Epub 2017 Sep 11.

Sophia Kinderziekenhuis,Department of Pediatric Cardiology,Erasmus Medical Centre Rotterdam,Rotterdam,The Netherlands.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1017/S1047951117001846DOI Listing
February 2018

Clinical Characteristics and Long-Term Outcome of Hypertrophic Cardiomyopathy in Individuals With a MYBPC3 (Myosin-Binding Protein C) Founder Mutation.

Circ Cardiovasc Genet 2017 Aug;10(4)

From the Department of Cardiology, Thoraxcenter (H.G.v.V., A.F.L.S., M.M.), Department of Clinical Genetics (R.A.O., M.A.v.S.), and Department of Pediatrics (I.M.E.F.-M.), Erasmus Medical Center, Rotterdam, The Netherlands; Department of Physiology, Institute for Cardiovascular Research, VU University Medical Center, Amsterdam, The Netherlands (J.v.d.V.); and Netherlands Heart Institute, Utrecht (J.v.d.V.).

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1161/CIRCGENETICS.116.001660DOI Listing
August 2017