Fetal electrocardiography and artificial intelligence for prenatal detection of congenital heart disease

por de Vries, Ivar R., van Laar, Judith O. E. H., van der Hout‐van der Jagt, Marieke B., Clur, Sally‐Ann B., Vullings, Rik
Publicado 2023

A Potential Diagnostic Approach for Foetal Long-QT Syndrome, Developed and Validated in Children

por Vink, Arja Suzanne, Kuipers, Irene M., De Bruin-Bon, Rianne H. A. C. M., Wilde, Arthur A. M., Blom, Nico A., Clur, Sally-Ann B.
Publicado 2018

Childhood onset nexilin dilated cardiomyopathy: A heterozygous and a homozygous case

por Bruyndonckx, Luc, Vogelzang, Judith L., Bugiani, Marianna, Straver, Bart, Kuipers, Irene M., Onland, Wes, Nannenberg, Eline A., Clur, Sally‐Ann, & van der Crabben, Saskia N.
Publicado 2021

The Role of the Epinephrine Test in the Diagnosis and Management of Children Suspected of Having Congenital Long QT Syndrome

por Clur, Sally-Ann B., Chockalingam, Priya, Filippini, Luc H., Widyanti, Ari P., Van Cruijsen, Marc, Blom, Nico A., Alders, Mariel, Hofman, Nynke, Wilde, Arthur A. M.
Publicado 2009

The electrical heart axis of the fetus between 18 and 24 weeks of gestation: A cohort study

por Lempersz, Carlijn, Noben, Lore, Clur, Sally-Ann B., van den Heuvel, Edwin, Zhan, Zhouzhao, Haak, Monique, Oei, S. Guid, Vullings, Rik, van Laar, Judith O. E. H.
Publicado 2021

The standardized 12-lead fetal electrocardiogram of the healthy fetus in mid-pregnancy: A cross-sectional study

por Lempersz, Carlijn, van Laar, Judith O., Clur, Sally-Ann B., Verdurmen, Kim M., Warmerdam, Guy J., van der Post, Joris, Blom, Nico A., Delhaas, Tammo, Oei, S. Guid, Vullings, Rik
Publicado 2020

The prognosis of common arterial trunk from a fetal perspective: A prenatal cohort study and systematic literature review

por van Nisselrooij, Amber E. L., Herling, Lotta, Clur, Sally‐Ann, Linskens, Ingeborg H., Pajkrt, Eva, Rammeloo, Lukas A., ten Harkel, Arend D. J., Hazekamp, Mark G., Blom, Nico A., Haak, Monique C.
Publicado 2021

Diagnostic accuracy of the response to the brief tachycardia provoked by standing in children suspected for long QT syndrome

por Vink, Arja S., Hermans, Ben J.M., Pimenta, Joana, Peltenburg, Puck J., Filippini, Luc H.P.M., Hofman, Nynke, Clur, Sally-Ann B., Blom, Nico A., Wilde, Arthur A.M., Delhaas, Tammo, Postema, Pieter G.
Publicado 2021

Diagnostic Accuracy of the Standing Test in Adults Suspected for Congenital Long‐QT Syndrome

por Vink, Arja S., Hermans, Ben J. M., Hooglugt, Jean‐Luc Q., Peltenburg, Puck J., Meijborg, Veronique M. F., Hofman, Nynke, Clur, Sally‐Ann B., Blom, Nico A., Delhaas, Tammo, Wilde, Arthur A. M., Postema, Pieter G.
Publicado 2023

Early Detection of Isolated Severe Congenital Heart Defects Is Associated with a Lower Threshold to Terminate the Pregnancy

por Lugthart, Malou A., Verbaarschot, Elvire, van Nisselrooij, Amber E. L., van de Kamp, Karline, Kleinrouweler, Emily, Haak, Monique C., Rozendaal, Lieke, Linskens, Ingeborg, Hruda, Jarda, Snijders, Rosalinde J. M., van Leeuwen, Elisabeth, Clur, Sally-Ann, Pajkrt, Eva
Publicado 2023

Repeatability of ventricular arrhythmia characteristics on the exercise-stress test in RYR2-mediated catecholaminergic polymorphic ventricular tachycardia

por Peltenburg, Puck J, Pultoo, Sanjeev N J, Tobert, Kathryn E, Bos, J Martijn, Lieve, Krystien V V, Tanck, Michael, Clur, Sally-Ann B, Blom, Nico A, Ackerman, Michael J, Wilde, Arthur A M, van der Werf, Christian
Publicado 2022

Manual vs. automatic assessment of the QT-interval and corrected QT

por Neumann, Benjamin, Vink, A Suzanne, Hermans, Ben J M, Lieve, Krystien V V, Cömert, Didem, Beckmann, Britt-Maria, Clur, Sally-Ann B, Blom, Nico A, Delhaas, Tammo, Wilde, Arthur A M, Kääb, Stefan, Postema, Pieter G, Sinner, Moritz F
Publicado 2023

Transposition of the great arteries: Fetal pulmonary valve growth and postoperative neo‐aortic root dilatation

por van der Palen, Roel L.F., van der Zee, Carlijn, Vink, Arja S., Knobbe, Ingmar, Jurgens, Sean J., van Leeuwen, Elizabeth, Bax, Caroline J., du Marchie Sarvaas, Gideon J., Blom, Nico A., Haak, Monique C., Bilardo, Caterina M., Clur, Sally‐Ann B.
Publicado 2019

The prevalence of genetic diagnoses in fetuses with severe congenital heart defects

por van Nisselrooij, Amber E. L., Lugthart, Malou A., Clur, Sally-Ann, Linskens, Ingeborg H., Pajkrt, Eva, Rammeloo, Lukas A., Rozendaal, Lieke, Blom, Nico A., van Lith, Jan M. M., Knegt, Alida C., Hoffer, Mariëtte J. V., Aten, Emmelien, Santen, Gijs W. E., Haak, Monique C.
Publicado 2020

GATA6 mutations: Characterization of two novel patients and a comprehensive overview of the GATA6 genotypic and phenotypic spectrum

por Škorić‐Milosavljević, Doris, Tjong, Fleur V. Y., Barc, Julien, Backx, Ad P. C. M., Clur, Sally‐Ann B., van Spaendonck‐Zwarts, Karin, Oostra, Roelof‐Jan, Lahrouchi, Najim, Beekman, Leander, Bökenkamp, Regina, Barge‐Schaapveld, Daniela Q. C. M., Mulder, Barbara J., Lodder, Elisabeth M., Bezzina, Connie R., Postma, Alex V.
Publicado 2019

Effects of cohort, genotype, variant, and maternal β-blocker treatment on foetal heart rate predictors of inherited long QT syndrome

por Kaizer, Alexander M, Winbo, Annika, Clur, Sally-Ann B, Etheridge, Susan P, Ackerman, Michael J, Horigome, Hitoshi, Herberg, Ulrike, Dagradi, Federica, Spazzolini, Carla, Killen, Stacy A S, Wacker-Gussmann, Annette, Wilde, Arthur A M, Sinkovskaya, Elena, Abuhamad, Alfred, Torchio, Margherita, Ng, Chai-Ann, Rydberg, Annika, Schwartz, Peter J, Cuneo, Bettina F
Publicado 2023

Germline variants in HEY2 functional domains lead to congenital heart defects and thoracic aortic aneurysms

por van Walree, Eva S., Dombrowsky, Gregor, Jansen, Iris E., Mirkov, Maša Umićević, Zwart, Rob, Ilgun, Aho, Guo, Dongchuan, Clur, Sally-Ann B., Amin, Ahmed S., Savage, Jeanne E., van der Wal, Allard C., Waisfisz, Quinten, Maugeri, Alessandra, Wilsdon, Anna, Bu’Lock, Frances A., Hurles, Matthew E., Dittrich, Sven, Berger, Felix, Martinez, Enrique Audain, Christoffels, Vincent M., Hitz, Marc-Philip, Milewicz, Dianna M., Posthuma, Daniëlle, Meijers-Heijboer, Hanne, Postma, Alex V., Mathijssen, Inge B.
Publicado 2021

Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot

por Škorić-Milosavljević, Doris, Lahrouchi, Najim, Bosada, Fernanda M., Dombrowsky, Gregor, Williams, Simon G., Lesurf, Robert, Tjong, Fleur V. Y., Walsh, Roddy, El Bouchikhi, Ihssane, Breckpot, Jeroen, Audain, Enrique, Ilgun, Aho, Beekman, Leander, Ratbi, Ilham, Strong, Alanna, Muenke, Maximilian, Heide, Solveig, Muir, Alison M., Hababa, Mariam, Cross, Laura, Zhou, Dihong, Pastinen, Tomi, Zackai, Elaine, Atmani, Samir, Ouldim, Karim, Adadi, Najlae, Steindl, Katharina, Rauch, Anita, Brook, David, Wilsdon, Anna, Kuipers, Irene, Blom, Nico A., Mulder, Barbara J., Mefford, Heather C., Keren, Boris, Joset, Pascal, Kruszka, Paul, Thiffault, Isabelle, Sheppard, Sarah E., Roberts, Amy, Lodder, Elisabeth M., Keavney, Bernard D., Clur, Sally-Ann B., Mital, Seema, Hitz, Marc-Philip, Christoffels, Vincent M., Postma, Alex V., Bezzina, Connie R.
Publicado 2021

Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot

por Škorić-Milosavljević, Doris, Lahrouchi, Najim, Bosada, Fernanda M., Dombrowsky, Gregor, Williams, Simon G., Lesurf, Robert, Tjong, Fleur V. Y., Walsh, Roddy, El Bouchikhi, Ihssane, Breckpot, Jeroen, Audain, Enrique, Ilgun, Aho, Beekman, Leander, Ratbi, Ilham, Strong, Alanna, Muenke, Maximilian, Heide, Solveig, Muir, Alison M., Hababa, Mariam, Cross, Laura, Zhou, Dihong, Pastinen, Tomi, Zackai, Elaine, Atmani, Samir, Ouldim, Karim, Adadi, Najlae, Steindl, Katharina, Rauch, Anita, Brook, David, Wilsdon, Anna, Kuipers, Irene, Blom, Nico A., Mulder, Barbara J., Mefford, Heather C., Keren, Boris, Joset, Pascal, Kruszka, Paul, Thiffault, Isabelle, Sheppard, Sarah E., Roberts, Amy, Lodder, Elisabeth M., Keavney, Bernard D., Clur, Sally-Ann B., Mital, Seema, Hitz, Marc-Philip, Christoffels, Vincent M., Postma, Alex V., Bezzina, Connie R.
Publicado 2021

Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries

por Škorić-Milosavljević, Doris, Tadros, Rafik, Bosada, Fernanda M., Tessadori, Federico, van Weerd, Jan Hendrik, Woudstra, Odilia I., Tjong, Fleur V.Y., Lahrouchi, Najim, Bajolle, Fanny, Cordell, Heather J., Agopian, A.J., Blue, Gillian M., Barge-Schaapveld, Daniela Q.C.M., Gewillig, Marc, Preuss, Christoph, Lodder, Elisabeth M., Barnett, Phil, Ilgun, Aho, Beekman, Leander, van Duijvenboden, Karel, Bokenkamp, Regina, Müller-Nurasyid, Martina, Vliegen, Hubert W., Konings, Thelma C., van Melle, Joost P., van Dijk, Arie P.J., van Kimmenade, Roland R.J., Roos-Hesselink, Jolien W., Sieswerda, Gertjan T., Meijboom, Folkert, Abdul-Khaliq, Hashim, Berger, Felix, Dittrich, Sven, Hitz, Marc-Phillip, Moosmann, Julia, Riede, Frank-Thomas, Schubert, Stephan, Galan, Pilar, Lathrop, Mark, Munter, Hans M., Al-Chalabi, Ammar, Shaw, Christopher E., Shaw, Pamela J., Morrison, Karen E., Veldink, Jan H., van den Berg, Leonard H., Evans, Sylvia, Nobrega, Marcelo A., Aneas, Ivy, Radivojkov-Blagojević, Milena, Meitinger, Thomas, Oechslin, Erwin, Mondal, Tapas, Bergin, Lynn, Smythe, John F., Altamirano-Diaz, Luis, Lougheed, Jane, Bouma, Berto J., Chaix, Marie-A., Kline, Jennie, Bassett, Anne S., Andelfinger, Gregor, van der Palen, Roel L.F., Bouvagnet, Patrice, Clur, Sally-Ann B., Breckpot, Jeroen, Kerstjens-Frederikse, Wilhelmina S., Winlaw, David S., Bauer, Ulrike M.M., Mital, Seema, Goldmuntz, Elizabeth, Keavney, Bernard, Bonnet, Damien, Mulder, Barbara J., Tanck, Michael W.T., Bakkers, Jeroen, Christoffels, Vincent M., Boogerd, Cornelis J., Postma, Alex V., Bezzina, Connie R.
Publicado 2021