Zobrazeno 1 - 10
of 97
pro vyhledávání: '"S. A. Clur"'
Publikováno v:
Bet, B B, de Vries, J M, Limpens, J, van Wely, M, van Leeuwen, E, Clur, S A & Pajkrt, E 2022, ' Implications of fetal premature atrial contractions : systematic review ', Ultrasound in Obstetrics and Gynecology, vol. 60, no. 6, pp. 721-730 . https://doi.org/10.1002/uog.26017
Fetal heart-rate irregularities occur in 1-2% of pregnancies and are usually caused by premature atrial contractions (PAC). Although PAC are considered benign, they may be associated with cardiac defects and tachyarrhythmia. We aimed to determine the
Autor:
C. M. de Vet, N. H. M. van Oostrum, S. B. Clur, D. A. A. van der Woude, S. G. Oei, J. O. E. H. van Laar
Publikováno v:
Ultrasound in Obstetrics and Gynecology, 61(2), 275-277. Wiley
Re: Fetal myocardial deformation measured with two-dimensional speckle-tracking echocardiography: longitudinal prospective cohort study of 124 healthy fetuses
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d628a54f5c763cab7c6c04e30ace7dbc
https://research.tue.nl/nl/publications/a2ad9e71-d7fd-44e0-995a-14cd9563f7b6
https://research.tue.nl/nl/publications/a2ad9e71-d7fd-44e0-995a-14cd9563f7b6
Autor:
Anouk S Moerdijk, Nathalie HP Claessens, Inge M van Ooijen, Pim van Ooij, Thomas Alderliesten, Heynric B Grotenhuis, MN Bekker, MJNL Benders, AE Bohte, JMPJ Breur, D Charisopoulou, S-A Clur, JMJ Cornette, Z Fejzic, MTM Franssen, S Frerich, LM Geerdink, ATJI Go, S Gommers, WA Helbing, A Hirsch, RJ Holtackers, WM Klein, GJ Krings, HJ Lamb, M Nijman, E Pajkrt, RN Planken, EM Schrauben, TJ Steenhuis, H ter Heide, WYR Vanagt, IM van Beynum, MD van Gaalen, GG van Iperen, J van Schuppen, TP Willems, I Witters
Publikováno v:
The Lancet Child & Adolescent Health, 7, 1, pp. 59-68
FUTURE 2.0 consortium 2023, ' Fetal MRI of the heart and brain in congenital heart disease ', The Lancet Child and Adolescent Health, vol. 7, no. 1, pp. 59-68 . https://doi.org/10.1016/S2352-4642(22)00249-8
The Lancet Child & Adolescent Health, 7, 59-68
FUTURE 2.0 consortium 2023, ' Fetal MRI of the heart and brain in congenital heart disease ', The Lancet Child and Adolescent Health, vol. 7, no. 1, pp. 59-68 . https://doi.org/10.1016/S2352-4642(22)00249-8
The Lancet Child & Adolescent Health, 7, 59-68
Item does not contain fulltext Antenatal assessment of congenital heart disease and associated anomalies by ultrasound has improved perinatal care. Fetal cardiovascular MRI and fetal brain MRI are rapidly evolving for fetal diagnostic testing of cong
Autor:
Noortje H M van Oostrum, Judith O E H van Laar, Kris Derks, Daisy A. A. van der Woude, S. Guid Oei, S. A. Clur
Publikováno v:
European Journal of Obstetrics & Gynecology and Reproductive Biology, 254, 87-94. Elsevier
Background Fetal growth restriction (FGR), defined as an estimated fetal weight (EFW)95th percentile (n = 1) compared to AGA fetuses. Strain rate was measured in two studies. One reported an increased strain rate, another showed comparable strain rat
Autor:
Arja S. Vink, Lukas A. J. Rammeloo, S. A. Clur, Nico A. Blom, Janneke A.E. Kammeraad, Arthur A.M. Wilde, Hans J.M.P.J. Breur, Puck Peltenburg
Publikováno v:
Circulation, 89-91. Lippincott Williams and Wilkins
STARTPAGE=89;ENDPAGE=91;ISSN=0009-7322;TITLE=Circulation
Circulation, 142(1), 89-91. Lippincott Williams & Wilkins
Peltenburg, P J, Blom, N A, Vink, A S, Kammeraad, J A E, Breur, H J M P J, Rammeloo, L A J, Wilde, A A M & Clur, S A B 2020, ' In Children and Adolescents from Brugada Syndrome-Families, only SCN5A Mutation Carriers Develop a Type-1 ECG Pattern Induced by Fever ', Circulation, pp. 89-91 . https://doi.org/10.1161/CIRCULATIONAHA.120.045720
Circulation, 142(1), 89-91. Lippincott Williams and Wilkins
STARTPAGE=89;ENDPAGE=91;ISSN=0009-7322;TITLE=Circulation
Circulation, 142(1), 89-91. Lippincott Williams & Wilkins
Peltenburg, P J, Blom, N A, Vink, A S, Kammeraad, J A E, Breur, H J M P J, Rammeloo, L A J, Wilde, A A M & Clur, S A B 2020, ' In Children and Adolescents from Brugada Syndrome-Families, only SCN5A Mutation Carriers Develop a Type-1 ECG Pattern Induced by Fever ', Circulation, pp. 89-91 . https://doi.org/10.1161/CIRCULATIONAHA.120.045720
Circulation, 142(1), 89-91. Lippincott Williams and Wilkins
Autor:
Gijs W. E. Santen, Damara Ortiz, Elisabeth M. Lodder, Francesca Clementina Radio, Michael V. Airola, Monique C. Haak, Dominic S Zimmerman, Quinn Gunst, Peter de Knijff, Katherine H. Kim, Viktor Stránecký, Stanislav Kmoch, Hiba Mustafa, Dmitriy Niyazov, H. Alex Brown, Najim Lahrouchi, Jamille Y. Robinson, Rick H. de Leeuw, Anne Sophie Denommé-Pichon, Sara Cherny, George A. Tanteles, Mariam Hababa, Joey V. Barnett, Doris Škorić-Milosavljević, Annemiek C. Dutman, Timothy J. Moss, Daniel M. de Laughter, Connie R. Bezzina, Zeev Perles, Fleur V.Y. Tjong, Matthew Ambrose, Forrest Z. Bowling, Arend D. J. ten Harkel, Katelijne Bouman, Barry Wolf, Monia Magliozzi, Asaf Ta-Shma, Lenka Piherová, Aho Ilgun, Sabrina C. Burn, Orly Elpeleg, Michael A. Frohman, Alex V. Postma, Maurice J.B. van den Hoff, Christian M. Salazar, Johanna C. Herkert, Christine Francannet, Jennifer Jacober, Andreas Rousounides, Leander Beekman, Barbara J.M. Mulder, Viktor Tomek, Bruel Ange-Line, Aphrodite Aristidou-Kallika, S. A. Clur, Gwendolyn T. R. Manten
Publikováno v:
CLIN Journal, 131(5):142148. AMER SOC CLINICAL INVESTIGATION INC
Journal of clinical investigation, 131(5):e142148. The American Society for Clinical Investigation
J Clin Invest
Journal of Clinical Investigation, 131(5). AMER SOC CLINICAL INVESTIGATION INC
Journal of clinical investigation, 131(5):e142148. The American Society for Clinical Investigation
J Clin Invest
Journal of Clinical Investigation, 131(5). AMER SOC CLINICAL INVESTIGATION INC
Congenital heart disease is the most common type of birth defect, accounting for one-third of all congenital anomalies. Using whole-exome sequencing of 2718 patients with congenital heart disease and a search in GeneMatcher, we identified 30 patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ef92ee7a5ecfb1bc070dbd1d6f217fa
https://hdl.handle.net/1887/3213006
https://hdl.handle.net/1887/3213006
Autor:
Matthew E. Hurles, Danielle Posthuma, Anna Wilsdon, Alex V. Postma, Inge B. Mathijssen, Dianna M. Milewicz, Alessandra Maugeri, Quinten Waisfisz, Aho Ilgun, Jeanne E. Savage, Marc Philip Hitz, Iris E. Jansen, Enrique Audain Martinez, Frances A. Bu'Lock, Felix Berger, Vincent M. Christoffels, Ahmed S. Amin, Rob Zwart, Maša Umićević Mirkov, Gregor Dombrowsky, Hanne Meijers-Heijboer, Eva S. van Walree, Allard C. van der Wal, S. A. Clur, Sven Dittrich, Dongchuan Guo
Publikováno v:
van Walree, E S, Dombrowsky, G, Jansen, I E, Umićević Mirkov, M, Zwart, R, Ilgun, A, Guo, D, Clur, S-A B, Amin, A S, Savage, J E, van der Wal, A C, Waisfisz, Q, Maugeri, A, Wilsdon, A, Bu'Lock, F A, Hurles, M E, Dittrich, S, Berger, F, Audain Martinez, E, Christoffels, V M, Hitz, M-P, Milewicz, D M, Posthuma, D, Meijers-Heijboer, H, Postma, A V & Mathijssen, I B 2022, ' Germline variants in HEY2 functional domains lead to congenital heart defects and thoracic aortic aneurysms ', Genetics in Medicine, vol. 24, no. 4, pp. 965-965 . https://doi.org/10.1016/j.gim.2022.01.018
van Walree, E S, Dombrowsky, G, Jansen, I E, Mirkov, M U, Zwart, R, Ilgun, A, Guo, D, Clur, S-A B, Amin, A S, Savage, J E, van der Wal, A C, Waisfisz, Q, Maugeri, A, Wilsdon, A, Bu’Lock, F A, Hurles, M E, Dittrich, S, Berger, F, Audain Martinez, E, Christoffels, V M, Hitz, M-P, Milewicz, D M, Posthuma, D, Meijers-Heijboer, H, Postma, A V & Mathijssen, I B 2021, ' Germline variants in HEY2 functional domains lead to congenital heart defects and thoracic aortic aneurysms ', Genetics in Medicine, vol. 23, no. 1, pp. 103-110 . https://doi.org/10.1038/s41436-020-00939-4
Genetics in Medicine, 24(4), 965-965. Lippincott Williams and Wilkins
Genetics in medicine, 23(1), 103-110. Lippincott Williams and Wilkins
Genetics in medicine : official journal of the American College of Medical Genetics
Genetics in Medicine, 23(1), 103-110. Lippincott Williams and Wilkins
van Walree, E S, Dombrowsky, G, Jansen, I E, Mirkov, M U, Zwart, R, Ilgun, A, Guo, D, Clur, S A B, Amin, A S, Savage, J E, van der Wal, A C, Waisfisz, Q, Maugeri, A, Wilsdon, A, Bu’Lock, F A, Hurles, M E, Dittrich, S, Berger, F, Audain Martinez, E, Christoffels, V M, Hitz, M P, Milewicz, D M, Posthuma, D, Meijers-Heijboer, H, Postma, A V & Mathijssen, I B 2021, ' Germline variants in HEY2 functional domains lead to congenital heart defects and thoracic aortic aneurysms ', Genetics in Medicine, vol. 23, no. 1, pp. 103-110 . https://doi.org/10.1038/s41436-020-00939-4
van Walree, E S, Dombrowsky, G, Jansen, I E, Mirkov, M U, Zwart, R, Ilgun, A, Guo, D, Clur, S-A B, Amin, A S, Savage, J E, van der Wal, A C, Waisfisz, Q, Maugeri, A, Wilsdon, A, Bu’Lock, F A, Hurles, M E, Dittrich, S, Berger, F, Audain Martinez, E, Christoffels, V M, Hitz, M-P, Milewicz, D M, Posthuma, D, Meijers-Heijboer, H, Postma, A V & Mathijssen, I B 2021, ' Germline variants in HEY2 functional domains lead to congenital heart defects and thoracic aortic aneurysms ', Genetics in Medicine, vol. 23, no. 1, pp. 103-110 . https://doi.org/10.1038/s41436-020-00939-4
Genetics in Medicine, 24(4), 965-965. Lippincott Williams and Wilkins
Genetics in medicine, 23(1), 103-110. Lippincott Williams and Wilkins
Genetics in medicine : official journal of the American College of Medical Genetics
Genetics in Medicine, 23(1), 103-110. Lippincott Williams and Wilkins
van Walree, E S, Dombrowsky, G, Jansen, I E, Mirkov, M U, Zwart, R, Ilgun, A, Guo, D, Clur, S A B, Amin, A S, Savage, J E, van der Wal, A C, Waisfisz, Q, Maugeri, A, Wilsdon, A, Bu’Lock, F A, Hurles, M E, Dittrich, S, Berger, F, Audain Martinez, E, Christoffels, V M, Hitz, M P, Milewicz, D M, Posthuma, D, Meijers-Heijboer, H, Postma, A V & Mathijssen, I B 2021, ' Germline variants in HEY2 functional domains lead to congenital heart defects and thoracic aortic aneurysms ', Genetics in Medicine, vol. 23, no. 1, pp. 103-110 . https://doi.org/10.1038/s41436-020-00939-4
Purpose: In this study we aimed to establish the genetic cause of a myriad of cardiovascular defects prevalent in individuals from a genetically isolated population, who were found to share a common ancestor in 1728. Methods: Trio genome sequencing w
Autor:
Akash R. Patel, Michelle E. Lee, Reina B Tan, Georgia Sarquella-Brugada, Mani Ram Krishna, Seshadri Balaji, Andrew P. Landstrom, Kalyanam Shivkumar, Kara S. Motonaga, Jeremy P. Moore, Prince J. Kannankeril, Maully J. Shah, Peter J. Schwartz, Federica Dagradi, Ming-Lon Young, Peter S. Fischbach, Kevin Shannon, Allison C. Hill, Saad Siddiqui, Shubhayan Sanatani, Elizabeth A. Stephenson, Michael J. Ackerman, Christina Y. Miyake, Susan P. Etheridge, Elham Sadeghi, Ronald T. Wakai, Hitoshi Horigome, Richard J. Czosek, Shashank Behere, S. A. Clur, Janette F. Strasburger, Matthew R. Williams, J. Martijn Bos, Roberto G. Gallotti
Publikováno v:
JACC Clin Electrophysiol
JACC: Clinical Electrophysiology
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
JACC. Clinical electrophysiology, vol 6, iss 12
JACC: Clinical Electrophysiology, 6(12), 1561-1570. Elsevier USA
JACC: Clinical Electrophysiology
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
JACC. Clinical electrophysiology, vol 6, iss 12
JACC: Clinical Electrophysiology, 6(12), 1561-1570. Elsevier USA
ObjectivesThis study sought to determine the relationship between long QT syndrome (LQTS) subtype (LTQ1, LTQ2, LTQ3) and postnatal cardiac events (CEs).BackgroundLQTS presenting with 2:1 atrioventricular block or torsades de pointes in the fetus and/
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3698b5dd8c510e72ab991fc703cea423
https://europepmc.org/articles/PMC7679474/
https://europepmc.org/articles/PMC7679474/
Autor:
Aalbertine K. Teunissen, S. A. Clur, Lukas A. Rammeloo, J.M.M. van Lith, Eva Pajkrt, Monique C. Haak, Ingeborg H. Linskens, A. E.L. van Nisselrooij, Lieke Rozendaal, Nico A. Blom
Publikováno v:
van Nisselrooij, A E L, Teunissen, A K K, Clur, S A, Rozendaal, L, Pajkrt, E, Linskens, I H, Rammeloo, L, van Lith, J M M, Blom, N A & Haak, M C 2020, ' Why are congenital heart defects being missed? ', Ultrasound in Obstetrics and Gynecology, vol. 55, no. 6, pp. 747-757 . https://doi.org/10.1002/uog.20358
Ultrasound in Obstetrics and Gynecology, 55(6), 747-757. John Wiley and Sons Ltd
Ultrasound in obstetrics & gynecology, 55(6), 747-757. John Wiley and Sons Ltd
Ultrasound in Obstetrics & Gynecology, 55(6), 747-757. WILEY
Ultrasound in Obstetrics and Gynecology, 55(6), 747-757. John Wiley and Sons Ltd
Ultrasound in obstetrics & gynecology, 55(6), 747-757. John Wiley and Sons Ltd
Ultrasound in Obstetrics & Gynecology, 55(6), 747-757. WILEY
OBJECTIVE Congenital heart defects (CHD) are still missed frequently in prenatal screening programs, which can result in severe morbidity or even death. The aim of this study was to evaluate the quality of fetal heart images, obtained during the seco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64040c71528c6ad1864ee06bce6516a9
https://hdl.handle.net/1887/3182155
https://hdl.handle.net/1887/3182155
Autor:
A. E.L. van Nisselrooij, J.M.M. van Lith, Eva Pajkrt, Lukas A. Rammeloo, Lieke Rozendaal, Nico A. Blom, Fenna A. R. Jansen, S. A. Clur, N. van Geloven, Monique C. Haak, Ingeborg H. Linskens
Publikováno v:
van Nisselrooij, A E L, Jansen, F A R, van Geloven, N, Linskens, I H, Pajkrt, E, Clur, S A, Rammeloo, L A, Rozendaal, L, van Lith, J M M, Blom, N A & Haak, M C 2020, ' Impact of extracardiac pathology on head growth in fetuses with congenital heart defect ', Ultrasound in Obstetrics and Gynecology, vol. 55, no. 2, pp. 217-225 . https://doi.org/10.1002/uog.20260
Ultrasound in Obstetrics & Gynecology
Ultrasound in Obstetrics and Gynecology, 55(2), 217-225. John Wiley and Sons Ltd
Ultrasound in Obstetrics & Gynecology, 55(2), 217-225. WILEY
Ultrasound in obstetrics & gynecology, 55(2), 217-225. John Wiley and Sons Ltd
Ultrasound in Obstetrics & Gynecology
Ultrasound in Obstetrics and Gynecology, 55(2), 217-225. John Wiley and Sons Ltd
Ultrasound in Obstetrics & Gynecology, 55(2), 217-225. WILEY
Ultrasound in obstetrics & gynecology, 55(2), 217-225. John Wiley and Sons Ltd
Objective Neurodevelopmental delay is frequently encountered in children with a congenital heart defect (CHD). Fetuses with major CHD have a smaller head circumference (HC), irrespective of altered cerebral flow or brain oxygenation. This cohort stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ccd3323516082875ae8caab6b89cdda5
https://hdl.handle.net/1887/3181614
https://hdl.handle.net/1887/3181614