Zobrazeno 1 - 6
of 6
pro vyhledávání: '"F H M Van Lint"'
Autor:
M Y C Van Der Heide, T E Verstraelen, F H M Van Lint, L P Bosman, R De Brouwer, V M Proost, T Germans, C Dickhoff, B A Schoonderwoerd, A C Houweling, J R Gimeno-Blanes, R A De Boer, M G P J Cox, P Van Tintelen, A A M Wilde
Publikováno v:
Europace. 25
Funding Acknowledgements Type of funding sources: Public Institution(s). Main funding source(s): PSIDER (ZOn-MW) PREDICT2 (Hartstichting) Background: The PLN p.Arg14del risk model is a mutation-specific risk model developed to predict individual mali
Autor:
M Van Der Heide, T E Verstraelen, F H M Van Lint, L P Bosman, R De Brouwer, V M Proost, G S Abeln, B A Schoonderwoerd, A C Houweling, J R Gimeno-Blanes, F W Asselbergs, R A De Boer, M P Van Den Berg, J P Van Tintelen, A A M Wilde
Publikováno v:
European Heart Journal. 43
Background/Introduction Recently, a variant-specific prediction model for PLN p.Arg14del variant carriers was developed to predict individual malignant ventricular arrhythmia (VA) risk to inform decision-making for primary prevention implantable card
Autor:
Marielle Alders, F. H. M. van Lint, Olaf R.F. Mook, Imke Christiaans, Hennie Bikker, R. H. Lekanne Deprez
Publikováno v:
Netherlands Heart Journal
Netherlands Heart Journal, 27(6), 304-309. Bohn Stafleu van Loghum
Netherlands heart journal, 27(6), 304-309. Bohn Stafleu van Loghum
Netherlands Heart Hournal, 27(6), 304-309. Bohn, Stafleu, Van Loghum
van Lint, F H M, Mook, O R F, Alders, M, Bikker, H, Lekanne dit Deprez, R H & Christiaans, I 2019, ' Large next-generation sequencing gene panels in genetic heart disease: yield of pathogenic variants and variants of unknown significance ', Netherlands Heart Journal, vol. 27, no. 6, pp. 304-309 . https://doi.org/10.1007/s12471-019-1250-5
Netherlands Heart Journal, 27(6), 304-309. Bohn Stafleu van Loghum
Netherlands heart journal, 27(6), 304-309. Bohn Stafleu van Loghum
Netherlands Heart Hournal, 27(6), 304-309. Bohn, Stafleu, Van Loghum
van Lint, F H M, Mook, O R F, Alders, M, Bikker, H, Lekanne dit Deprez, R H & Christiaans, I 2019, ' Large next-generation sequencing gene panels in genetic heart disease: yield of pathogenic variants and variants of unknown significance ', Netherlands Heart Journal, vol. 27, no. 6, pp. 304-309 . https://doi.org/10.1007/s12471-019-1250-5
Background Genetic heterogeneity is common in inherited cardiac diseases. Next-generation sequencing gene panels are therefore suitable for genetic diagnosis. We describe the results of implementation of cardiomyopathy and arrhythmia gene panels in c
Autor:
K. Taha, L. M. Van den Heuvel, R. W. Roudijk, Imke Christiaans, M. Bourfiss, Carol Ann Remme, T. A. B. van Veen, J. P. van Tintelen, M. J. Boonstra, F. H. M. van Lint, Peter Loh, Folkert W. Asselbergs, S. M. van der Voorn, M.P. van den Berg, A. S. J. M. te Riele, Laurens P Bosman
Publikováno v:
Netherlands Heart Journal
In relatives of index patients with dilated cardiomyopathy and arrhythmogenic cardiomyopathy, early detection of disease onset is essential to prevent sudden cardiac death and facilitate early treatment of heart failure. However, the optimal screenin
Autor:
B. G. S. Abeln, J. P. van Tintelen, Folkert W. Asselbergs, Laurens P Bosman, Tom E Verstraelen, P. A. van der Zwaag, Arthur A.M. Wilde, M.P. van den Berg, F. H. M. van Lint
Publikováno v:
European Heart Journal. 40
Background/Introduction The founder mutation p.Arg14del in the gene encoding phospholamban (PLN) is a known cause of arrhythmogenic cardiomyopathy (ACM) with distinct clinical features, such as microvoltages on the ECG and right or left ventricular d
Autor:
Merryn V. E. Macville, F. H. M. van Lint, P. C. Krapels, Antonio W. D. Gavilanes, J. W. Weber, John J.M. Engelen, Alexander P.A. Stegmann, Suzanna G.M. Frints, Ctrm Schrander-Stumpel, Christine Willekes, Yvonne J. Vos, Jaap A. Bakker, Judith M.A. Verhagen, C. E. M. De Die-Smulders
Publikováno v:
European Journal of Medical Genetics, 54(6), E542-E547. Elsevier
European journal of medical genetics, 54(6), E542-E547. ELSEVIER SCIENCE BV
European Journal of Medical Genetics, 54(6), e542-e547. Elsevier Masson
European journal of medical genetics, 54(6), E542-E547. ELSEVIER SCIENCE BV
European Journal of Medical Genetics, 54(6), e542-e547. Elsevier Masson
Congenital hydrocephalus is a common and often disabling disorder. The etiology is very heterogeneous. Little is known about the genetic causes of congenital hydrocephalus.A retrospective survey was performed including patients with primary congenita