Search Results - Ingrid M.E. Frohn-Mulder

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  1. 1
    The efficacy of flecainide versus digoxin in the management of fetal supraventricular tachycardia

    The efficacy of flecainide versus digoxin in the management of fetal supraventricular tachycardia by Ingrid M.E. Frohn-Mulder, Patricia A. Stewart, Maarten Witsenburg, Nicolette S. den Hollander, J. W. Wladimiroff, John Hess

    Published 1995
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  2. 2
    Juxtaductal pulmonary artery coarctation

    Juxtaductal pulmonary artery coarctation by Nynke J. Elzenga, Robert Jan van Suylen, Ingrid M.E. Frohn-Mulder, C. E. Essed, Egbert Bos, J.M. Quaegebeur

    Published 1990
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  3. 3
    Management of fixed subaortic stenosis: A retrospective study of 57 cases

    Management of fixed subaortic stenosis: A retrospective study of 57 cases by Arie G. de Vries, John Hess, Maarten Witsenburg, Ingrid M.E. Frohn-Mulder, Ad J.J.C. Bogers, Egbert Bos

    Published 1992
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  4. 4
    Mucopolysaccharidosis: Cardiologic features and effects of enzyme‐replacement therapy in 24 children with MPS I, II and VI

    Mucopolysaccharidosis: Cardiologic features and effects of enzyme‐replacement therapy in 24 children with MPS I, II and VI by Marion M. Brands, Ingrid M.E. Frohn-Mulder, M.L.C. Hagemans, Wim C.J. Hop, Esmée Oussoren, Willem A. Helbing, Ans T. van der Ploeg

    Published 2012
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  5. 5
    Outcomes of Contemporary Family Screening in Hypertrophic Cardiomyopathy

    Outcomes of Contemporary Family Screening in Hypertrophic Cardiomyopathy by Hannah G. van Velzen, Arend F. L. Schinkel, Sara J. Baart, Rogier A. Oldenburg, Ingrid M.E. Frohn-Mulder, Marjon A. van Slegtenhorst, Michelle Michels

    Published 2018
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  6. 6
    Compound heterozygous or homozygous truncating MYBPC3 mutations cause lethal cardiomyopathy with features of noncompaction and septal defects

    Compound heterozygous or homozygous truncating MYBPC3 mutations cause lethal cardiomyopathy with features of noncompaction and septal defects by Marja W. Wessels, Johanna C. Herkert, Ingrid M.E. Frohn-Mulder, Michiel Dalinghaus, Arthur van den Wijngaard, Ronald R. de Krijger, Michelle Michels, I.F.M. de Coo, Yvonne M. Hoedemaekers, Dennis Dooijes

    Published 2014
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  7. 7
    Familial Evaluation in Catecholaminergic Polymorphic Ventricular Tachycardia

    Familial Evaluation in Catecholaminergic Polymorphic Ventricular Tachycardia by Christian van der Werf, Ineke Nederend, Nynke Hofman, Nan van Geloven, Corné Ebink, Ingrid M.E. Frohn-Mulder, A. Marco Alings, Hans A. Bosker, Frank Bracke, Freek van den Heuvel, Reinier A. Waalewijn, Hennie Bikker, J. Peter van Tintelen, Zahurul A. Bhuiyan, Maarten P. van den Berg, Arthur A.M. Wilde

    Published 2012
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  8. 8
    Aggressive Cardiovascular Phenotype of Aneurysms-Osteoarthritis Syndrome Caused by Pathogenic SMAD3 Variants

    Aggressive Cardiovascular Phenotype of Aneurysms-Osteoarthritis Syndrome Caused by Pathogenic SMAD3 Variants by Denise van der Linde, Ingrid M.B.H. van de Laar, Aida M. Bertoli‐Avella, Rogier A. Oldenburg, Jos A. Bekkers, Francesco Mattace‐Raso, Anton H. van den Meiracker, Adriaan Moelker, Fop van Kooten, Ingrid M.E. Frohn-Mulder, Janneke Timmermans, Els Moltzer, Jan M. Cobben, Lut Van Laer, Bart Loeys, Julie De Backer, Paul Coucke, Anne De Paepe, Yvonne Hilhorst‐Hofstee, Marja W. Wessels, Jolien W. Roos‐Hesselink

    Published 2012
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  9. 9
    Cardiovascular malformations caused by NOTCH1 mutations do not keep left: data on 428 probands with left-sided CHD and their families

    Cardiovascular malformations caused by NOTCH1 mutations do not keep left: data on 428 probands with left-sided CHD and their families by Wilhelmina S. Kerstjens‐Frederikse, Ingrid M.B.H. van de Laar, Yvonne J. Vos, Judith M.A. Verhagen, Rolf M.F. Berger, Klaske D. Lichtenbelt, Jolien S. Klein Wassink‐Ruiter, Paul A. van der Zwaag, Gideon J. du Marchie Sarvaas, Klasien A. Bergman, Catia M. Bilardo, Jolien W. Roos‐Hesselink, J. H. P. Janssen, Ingrid M.E. Frohn-Mulder, Karin Y. van Spaendonck‐Zwarts, Joost P. van Melle, Robert M.W. Hofstra, Marja W. Wessels

    Published 2016
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  10. 10
    <i>NPHP4</i> Variants Are Associated With Pleiotropic Heart Malformations

    <i>NPHP4</i> Variants Are Associated With Pleiotropic Heart Malformations by Vanessa French, Ingrid M.B.H. van de Laar, Marja W. Wessels, Christan F. Rohé, Jolien W. Roos‐Hesselink, Guangliang Wang, Ingrid M.E. Frohn-Mulder, Lies‐Anne Severijnen, Bianca M. de Graaf, Rachel Schot, Guido J. Breedveld, Edwin Mientjes, Marianne van Tienhoven, Elodie Jadot, Zhengxin Jiang, Annemieke J.M.H. Verkerk, Sigrid M.A. Swagemakers, Hanka Venselaar, Zohreh Rahimi, Hossein Najmabadi, Hanne Meijers-Heijboer, Esther de Graaff, Wim A. Helbing, Rob Willemsen, Koenraad Devriendt, John W. Belmont, Ben A. Oostra, Jeffrey D. Amack, Aida M. Bertoli‐Avella

    Published 2012
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  11. 11
    Biallelic Truncating Mutations in ALPK3 Cause Severe Pediatric Cardiomyopathy

    Biallelic Truncating Mutations in ALPK3 Cause Severe Pediatric Cardiomyopathy by Rowida Almomani, Judith M.A. Verhagen, Johanna C. Herkert, Erwin Brosens, Karin Y. van Spaendonck‐Zwarts, Angeliki Asimaki, Paul A. van der Zwaag, Ingrid M.E. Frohn-Mulder, Aida M. Bertoli‐Avella, Ludolf G. Boven, Marjon A. van Slegtenhorst, Jasper J. van der Smagt, Wilfred F. J. van IJcken, Bert Timmer, Margriet van Stuijvenberg, Robert M. Verdijk, Jeffrey E. Saffitz, Frederik A. du Plessis, Michelle Michels, Robert M.W. Hofstra, Richard J. Sinke, J. Peter van Tintelen, Marja W. Wessels, Jan D.H. Jongbloed, Ingrid M.B.H. van de Laar

    Published 2016
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