Search Results - Karin Y. van Spaendonck‐Zwarts

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  1. 1
    Pregnancy, cardiomyopathies, and genetics

    Pregnancy, cardiomyopathies, and genetics by J. Peter van Tintelen, Petronella G. Pieper, Karin Y. van Spaendonck‐Zwarts, Maarten P. van den Berg

    Published 2014
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  2. 2
    Genetic advances in sarcomeric cardiomyopathies: state of the art

    Genetic advances in sarcomeric cardiomyopathies: state of the art by Carolyn Y. Ho, Philippe Charron, Pascale Richard, Francesca Girolami, Karin Y. van Spaendonck‐Zwarts, Yigal M. Pinto

    Published 2015
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  3. 3
    PMP22 related neuropathies: Charcot-Marie-Tooth disease type 1A and Hereditary Neuropathy with liability to Pressure Palsies

    PMP22 related neuropathies: Charcot-Marie-Tooth disease type 1A and Hereditary Neuropathy with liability to Pressure Palsies by Barbara W. van Paassen, Anneke J. van der Kooi, Karin Y. van Spaendonck‐Zwarts, Camiel Verhamme, Frank Baas, Marianne de Visser

    Published 2014
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  4. 4
    Systematic review of pregnancy in women with inherited cardiomyopathies

    Systematic review of pregnancy in women with inherited cardiomyopathies by Sébastien P.J. Krul, Jasper J. van der Smagt, Maarten P. van den Berg, Krystyna M. Sollie, Petronella G. Pieper, Karin Y. van Spaendonck‐Zwarts

    Published 2011
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  5. 5
    Potential genetic predisposition for anthracycline-associated cardiomyopathy in families with dilated cardiomyopathy

    Potential genetic predisposition for anthracycline-associated cardiomyopathy in families with dilated cardiomyopathy by Marijke Wasielewski, Karin Y. van Spaendonck‐Zwarts, Nico-Derk L. Westerink, Jan D.H. Jongbloed, A. Postma, Jourik A. Gietema, J. Peter van Tintelen, Maarten P. van den Berg

    Published 2014
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  6. 6
    Peripartum Cardiomyopathy as a Part of Familial Dilated Cardiomyopathy

    Peripartum Cardiomyopathy as a Part of Familial Dilated Cardiomyopathy by Karin Y. van Spaendonck‐Zwarts, J. Peter van Tintelen, Dirk J. van Veldhuisen, Rik van der Werf, Jan D.H. Jongbloed, Walter J. Paulus, Dennis Dooijes, Maarten P. van den Berg

    Published 2010
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  7. 7
    Targeted Next-Generation Sequencing can Replace Sanger Sequencing in Clinical Diagnostics

    Targeted Next-Generation Sequencing can Replace Sanger Sequencing in Clinical Diagnostics by Birgit Sikkema‐Raddatz, Lennart Johansson, Eddy N. de Boer, Rowida Almomani, Ludolf G. Boven, Maarten P. van den Berg, Karin Y. van Spaendonck‐Zwarts, J. Peter van Tintelen, Rolf H. Sijmons, Jan D.H. Jongbloed, Richard J. Sinke

    Published 2013
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  8. 8
    RBM20 Mutations Induce an Arrhythmogenic Dilated Cardiomyopathy Related to Disturbed Calcium Handling

    RBM20 Mutations Induce an Arrhythmogenic Dilated Cardiomyopathy Related to Disturbed Calcium Handling by Maarten M. G. van den Hoogenhof, Abdelaziz Beqqali, Ahmad S. Amin, Ingeborg van der Made, Simona Aufiero, Mohsin A.F. Khan, Cees A. Schumacher, Joeri A. Jansweijer, Karin Y. van Spaendonck‐Zwarts, Carol Ann Remme, Johannes Backs, Arie O. Verkerk, Antonius Baartscheer, Yigal M. Pinto, Esther E. Creemers

    Published 2018
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  9. 9
    The yield of risk stratification for sudden cardiac death in hypertrophic cardiomyopathy myosin-binding protein C gene mutation carriers: focus on predictive screening

    The yield of risk stratification for sudden cardiac death in hypertrophic cardiomyopathy myosin-binding protein C gene mutation carriers: focus on predictive screening by Imke Christiaans, Erwin Birnie, Irene M. van Langen, Karin Y. van Spaendonck‐Zwarts, J. Peter van Tintelen, Maarten P. van den Berg, Douwe E. Atsma, Apollonia T.J.M. Helderman-van den Enden, Yigal M. Pinto, J.F. Hermans-van Ast, Gouke J. Bonsel, Arthur A.M. Wilde

    Published 2009
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  10. 10
    Recessive MYL2 mutations cause infantile type I muscle fibre disease and cardiomyopathy

    Recessive MYL2 mutations cause infantile type I muscle fibre disease and cardiomyopathy by Marian A. J. Weterman, P. G. Barth, Karin Y. van Spaendonck‐Zwarts, Eleonora Aronica, Bwee Tien Poll‐The, Oebele F. Brouwer, J. Peter van Tintelen, Zohal Qahar, Edward J. Bradley, Marit de Wissel, Leonardo Salviati, C. Angelini, Lambertus P. van den Heuvel, Yolande Thomasse, Ad Backx, Gudrun Nürnberg, Peter Nürnberg, Frank Baas

    Published 2013
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  11. 11
    Titin gene mutations are common in families with both peripartum cardiomyopathy and dilated cardiomyopathy

    Titin gene mutations are common in families with both peripartum cardiomyopathy and dilated cardiomyopathy by Karin Y. van Spaendonck‐Zwarts, Anna Pósafalvi, Maarten P. van den Berg, Denise Hilfiker‐Kleiner, Ilse A. E. Bollen, Karen Sliwa, Mariëlle Alders, Rowida Almomani, Irene M. van Langen, Peter van der Meer, Richard J. Sinke, Jolanda van der Velden, Dirk J. van Veldhuisen, J. Peter van Tintelen, Jan D.H. Jongbloed

    Published 2014
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  12. 12
    Pregnancy course and outcomes in women with arrhythmogenic right ventricular cardiomyopathy

    Pregnancy course and outcomes in women with arrhythmogenic right ventricular cardiomyopathy by Anke R. Hodes, Crystal Tichnell, Anneline S.J.M. te Riele, Brittney Murray, Judith A. Groeneweg, Abhishek C. Sawant, Stuart D. Russell, Karin Y. van Spaendonck‐Zwarts, Maarten P. van den Berg, Arthur A.M. Wilde, Harikrishna Tandri, Daniel P. Judge, Richard N.W. Hauer, Hugh Calkins, J. Peter van Tintelen, Cynthia A. James

    Published 2015
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  13. 13
    Additional genetic variants in cardiomyopathy patients with the pathogenic PLN p.(Arg14del) founder variant

    Additional genetic variants in cardiomyopathy patients with the pathogenic PLN p.(Arg14del) founder variant by Esmée van Drie, Jan D.H. Jongbloed, Edgar T. Hoorntje, Paul A. van der Zwaag, Moniek G.P.J. Cox, Ronald H. Lekanne Deprez, Arjan C. Houweling, Virginnio Proost, A. A. M. Wilde, Dennis Dooijes, Annette F. Baas, Anneline S.J.M. te Riele, Karin Y. van Spaendonck‐Zwarts, Elisabeth M. Lodder, J. Peter van Tintelen

    Published 2025
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  14. 14
    Severe cardiac phenotype with right ventricular predominance in a large cohort of patients with a single missense mutation in the DES gene

    Severe cardiac phenotype with right ventricular predominance in a large cohort of patients with a single missense mutation in the DES gene by J. Peter van Tintelen, Isabelle C Van Gelder, Angeliki Asimaki, Albert J.H. Suurmeijer, Ans C.P. Wiesfeld, Jan D.H. Jongbloed, Arthur van den Wijngaard, Jan B. M. Kuks, Karin Y. van Spaendonck‐Zwarts, Nicolette C. Notermans, Ludolf G. Boven, Freek van den Heuvel, Hermine E. Veenstra‐Knol, Jeffrey E. Saffitz, Robert M.W. Hofstra, Maarten P. van den Berg

    Published 2009
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  15. 15
    Renal cancer and pneumothorax risk in Birt–Hogg–Dubé syndrome; an analysis of 115 FLCN mutation carriers from 35 BHD families

    Renal cancer and pneumothorax risk in Birt–Hogg–Dubé syndrome; an analysis of 115 FLCN mutation carriers from 35 BHD families by Arjan C. Houweling, Lieke Gijezen, Marianne A. Jonker, Martijn B. A. van Doorn, Reinhard Oldenburg, Karin Y. van Spaendonck‐Zwarts, Edward M. Leter, T. A. van Os, Nicole C.T. van Grieken, Elisabeth H. Jaspars, M. M. de Jong, Ernie M.H.F. Bongers, Paul C. Johannesma, Pieter E. Postmus, R. Jeroen A. van Moorselaar, J-Htm van Waesberghe, Theo M. Starink, Maurice A. M. Van Steensel, Gilles Thomas, Fred H. Menko

    Published 2011
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  16. 16
    Truncating titin mutations are associated with a mild and treatable form of dilated cardiomyopathy

    Truncating titin mutations are associated with a mild and treatable form of dilated cardiomyopathy by Joeri A. Jansweijer, Karin Nieuwhof, Francesco Paolo Russo, Edgar T. Hoorntje, Jan D.H. Jongbloed, Ronald H. Lekanne Deprez, Alex V. Postma, Marieke Bronk, Ingrid A.W. van Rijsingen, Simone de Haij, Elena Biagini, Paul L. van Haelst, Jan van Wijngaarden, Maarten P. van den Berg, Arthur A.M. Wilde, Marcel M.A.M. Mannens, Rudolf A. de Boer, Karin Y. van Spaendonck‐Zwarts, J. Peter van Tintelen, Yigal M. Pinto

    Published 2016
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  17. 17
    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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  18. 18
    Genetics, Clinical Features, and Long-Term Outcome of Noncompaction Cardiomyopathy

    Genetics, Clinical Features, and Long-Term Outcome of Noncompaction Cardiomyopathy by Jaap I. van Waning, Kadir Çalişkan, Yvonne M. Hoedemaekers, Karin Y. van Spaendonck‐Zwarts, Annette F. Baas, S. Matthijs Boekholdt, Joost P. van Melle, Arco J. Teske, Folkert W. Asselbergs, Ad Backx, Gideon J. du Marchie Sarvaas, Michiel Dalinghaus, Johannes M. P. J. Breur, Marijke Linschoten, Laura A. Verlooij, Isabella Kardys, Dennis Dooijes, Ronald H. Lekanne Deprez, Arne IJpma, Maarten P. van den Berg, Robert M.W. Hofstra, Marjon A. van Slegtenhorst, Jan D.H. Jongbloed, Daniëlle Majoor‐Krakauer

    Published 2018
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  19. 19
    KIF1A variants are a frequent cause of autosomal dominant hereditary spastic paraplegia

    KIF1A variants are a frequent cause of autosomal dominant hereditary spastic paraplegia by Maartje Pennings, Meyke Schouten, Judith van Gaalen, Rowdy Meijer, Susanne T. de Bot, Marjolein Kriek, Christiaan G. J. Saris, Leonard H. van den Berg, Michael A. van Es, Dick M. H. Zuidgeest, Mariet W. Elting, Jiddeke M. van de Kamp, Karin Y. van Spaendonck‐Zwarts, Christine de Die‐Smulders, Eva H. Brilstra, Corien Verschuuren, Bert B.A. de Vries, Jacques Bruijn, Kalliopi Sofou, Floor A.M. Duijkers, Bregje Jaeger, Jolanda Schieving, Bart P.C. van de Warrenburg, Erik-Jan Kamsteeg

    Published 2019
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  20. 20
    Phospholamban R14del mutation in patients diagnosed with dilated cardiomyopathy or arrhythmogenic right ventricular cardiomyopathy: evidence supporting the concept of arrhythmogenic cardiomyopathy

    Phospholamban R14del mutation in patients diagnosed with dilated cardiomyopathy or arrhythmogenic right ventricular cardiomyopathy: evidence supporting the concept of arrhythmogeni... by Paul A. van der Zwaag, Ingrid A.W. van Rijsingen, Angeliki Asimaki, Jan D.H. Jongbloed, Dirk J. van Veldhuisen, Ans C.P. Wiesfeld, Moniek G.P.J. Cox, Laura T. van Lochem, Rudolf A. de Boer, Robert M.W. Hofstra, Imke Christiaans, Karin Y. van Spaendonck‐Zwarts, Ronald H. Lekanne Deprez, Daniel P. Judge, Hugh Calkins, Albert J.H. Suurmeijer, Richard N.W. Hauer, Jeffrey E. Saffitz, Arthur A.M. Wilde, Maarten P. van den Berg, J. Peter van Tintelen

    Published 2012
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