Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Bart, Straver"'
Autor:
Adinda G. H. Pijpers, Cunera M. C. de Beaufort, Sanne C. Maat, Chantal J. M. Broers, Bart Straver, Ernest van Heurn, Ramon R. Gorter, Joep P. M. Derikx
Publikováno v:
Children, Vol 10, Iss 4, p 688 (2023)
Background: Congenital abdominal wall defects might be associated with other anomalies, such as atresia in gastroschisis and cardiac anomalies in omphalocele patients. However, in the current literature, an overview of these additional anomalies and
Externí odkaz:
https://doaj.org/article/a8e218e15a9d406bbf27f3c139161d8f
Autor:
Adinda G. H. Pijpers, Laurens D. Eeftinck Schattenkerk, Bart Straver, Petra J. G. Zwijnenburg, Chantal J. M. Broers, Ernest L. W. Van Heurn, Ramon R. Gorter, Joep P. M. Derikx
Publikováno v:
Children, Vol 9, Iss 12, p 1814 (2022)
Background: Duodenal obstruction (DO) is a congenital anomaly that is highly associated with other anomalies, such as cardiac anomalies and trisomy 21. However, an overview of additional anomalies and patient-specific risk factors for cardiac anomali
Externí odkaz:
https://doaj.org/article/17aaddbf6ca842a7ad2a0d81492c5a16
Autor:
Jolien W Roos-Hesselink, Ad J J C Bogers, Johanna J M Takkenberg, Jonathan R G Etnel, Willem A Helbing, Regina The, Barbara J M Mulder, Philippine Kiès, Mark G Hazekamp, Nico A Blom, Lidia R Bons, Arie P J van Dijk, Martijn G Slieker, Frederiek De Heer, Daniëlle Robbers-Visser, Ingrid M Van Beynum, Bart Straver, Monique RM Jongbloed, Jolanda Kluin, Robin A Bertels, Elisabeth M W J Utens, Eugene Van Galen
Publikováno v:
Open Heart, Vol 8, Iss 1 (2021)
Background In response to an increased need for patient information in congenital heart disease, we previously developed an online, evidence-based information portal for patients with congenital aortic and pulmonary valve disease. To assess its effec
Externí odkaz:
https://doaj.org/article/972caf847cd846aa80b3f622f588df10
Autor:
Adinda G. H. Pijpers, Laurens D. Eeftinck Schattenkerk, Ralph de Vries, Chantal J. M. Broers, Bart Straver, Ernest L. W. van Heurn, Gijsbert D. Musters, Ramon R. Gorter, Joep P. M. Derikx
Publikováno v:
Pijpers, A G H, Eeftinck Schattenkerk, L D, de Vries, R, Broers, C J M, Straver, B, van Heurn, E L W, Musters, G D, Gorter, R R & Derikx, J P M 2023, ' Cardiac anomalies in children with congenital duodenal obstruction : a systematic review with meta-analysis ', Pediatric Surgery International, vol. 39, no. 1, 160, pp. 160 . https://doi.org/10.1007/s00383-023-05449-3
Background Cardiac anomalies occur frequently in patients with congenital duodenal obstruction (DO). However, the exact occurrence and the type of associated anomalies remain unknown. Therefore, the aim of this systematic review is to aggregate the a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c56f1363353899ada44059590c455fc2
https://research.vumc.nl/en/publications/8f127ed5-6b81-4e31-9fbf-1a3076e2cb2c
https://research.vumc.nl/en/publications/8f127ed5-6b81-4e31-9fbf-1a3076e2cb2c
Autor:
Jef Van den Eynde, Roel L F van der Palen, Ingmar Knobbe, Bart Straver, Lauran Stöger, Gabriella Ricciardi, Thelma C Konings, Monique R M Jongbloed, Mark G Hazekamp
Publikováno v:
van den Eynde, J, van der Palen, R L F, Knobbe, I, Straver, B, Stöger, L, Ricciardi, G, Konings, T C, Jongbloed, M R M & Hazekamp, M G 2023, ' Outcomes of the modified Yacoub aortocoronary flap technique for 'non-separable' single sinus coronary arteries with intramural course in the neonatal arterial switch operation ', European Journal of Cardio-thoracic Surgery, vol. 63, no. 5 . https://doi.org/10.1093/ejcts/ezad029
European Journal of Cardio-thoracic Surgery, 63(5). Elsevier
European Journal of Cardio-thoracic Surgery, 63(5). Elsevier
OBJECTIVES Coronary transfer remains the most crucial part of the arterial switch operation (ASO); yet, certain coronary anatomies prohibit the use of button or trap-door transfer techniques. In the rare setting of ‘non-separable’ single sinus co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d42f4af6b7f24fbf0f68a3a538a46b67
https://doi.org/10.1093/ejcts/ezad029
https://doi.org/10.1093/ejcts/ezad029
Autor:
Lars S. Witte, Abdelhak el Bouziani, Bart Straver, Karel T. Koch, Marcel A.M. Beijk, Leonie Caesar, Jan G.P. Tijssen, Berto J. Bouma, Robbert J. de Winter
Publikováno v:
Witte, L S, el Bouziani, A, Straver, B, Koch, K T, Beijk, M A M, Caesar, L, Tijssen, J G P, Bouma, B J & de Winter, R J 2022, ' Atrial Right-to-Left Shunting Does Not Predict PFO Orifice Area in Patients Undergoing Percutaneous PFO Closure ', JACC Cardiovascular Interventions, vol. 15, no. 21, pp. 2231-2233 . https://doi.org/10.1016/j.jcin.2022.05.014
JACC Cardiovascular Interventions, 15(21), 2231-2233. Elsevier Inc.
JACC. Cardiovascular interventions, 15(21), 2231-2233. Elsevier Inc.
JACC Cardiovascular Interventions, 15(21), 2231-2233. Elsevier Inc.
JACC. Cardiovascular interventions, 15(21), 2231-2233. Elsevier Inc.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ccc059266b54af256392bcca587b1827
https://doi.org/10.1016/j.jcin.2022.05.014
https://doi.org/10.1016/j.jcin.2022.05.014
Autor:
Irene M. Kuipers, R. N. Planken, A. E. van der Hulst, Bart Straver, S. M. Boekholdt, R. J. Oostra, J van Schuppen
Publikováno v:
Surgical and radiologic anatomy, 44(1), 99-103. Springer Paris
Surgical and Radiologic Anatomy
Surgical and Radiologic Anatomy
Introduction We present a case of dual drainage of the right upper lobe of the lung into the left atrium and via partial anomalous venous pulmonary return (PAPVR) into a persistent left superior vena cava (SVC). Discussion It is only in the minority
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ee2360af23e075a0f0d5c4bedc646be
https://doi.org/10.1007/s00276-021-02849-9
https://doi.org/10.1007/s00276-021-02849-9
Autor:
Mohammad Abdelghani, Martina Nassif, Nico A. Blom, Martijn S. Van Mourik, Bart Straver, David R. Koolbergen, Jolanda Kluin, Jan G. Tijssen, Barbara J. M. Mulder, Berto J. Bouma, Robbert J. de Winter
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 7, Iss 13 (2018)
Background Infective endocarditis (IE) after transcatheter pulmonary valve implantation (TPVI) in dysfunctioning right ventricular outflow tract conduits has evoked growing concerns. We aimed to investigate the incidence and the natural history of IE
Externí odkaz:
https://doaj.org/article/c9b8056f41544a12b107b67c31da227a
Autor:
Cunera M.C. de Beaufort, Alex C.M. van den Akker, Caroline F. Kuijper, Chantal J.M. Broers, Justin R. de Jong, Sjoerd A. de Beer, Bart Straver, Petra J.G. Zwijnenburg, Ramon R. Gorter
Publikováno v:
Journal of pediatric surgery. W.B. Saunders Ltd
de Beaufort, C M C, van den Akker, A C M, Kuijper, C F, Broers, C J M, de Jong, J R, de Beer, S A, Straver, B, Zwijnenburg, P J G & Gorter, R R 2023, ' The importance of screening for additional anomalies in patients with anorectal malformations : A retrospective cohort study ', Journal of Pediatric Surgery . https://doi.org/10.1016/j.jpedsurg.2022.11.010
Journal of Pediatric Surgery. W.B. Saunders Ltd
de Beaufort, C M C, van den Akker, A C M, Kuijper, C F, Broers, C J M, de Jong, J R, de Beer, S A, Straver, B, Zwijnenburg, P J G & Gorter, R R 2023, ' The importance of screening for additional anomalies in patients with anorectal malformations : A retrospective cohort study ', Journal of Pediatric Surgery . https://doi.org/10.1016/j.jpedsurg.2022.11.010
Journal of Pediatric Surgery. W.B. Saunders Ltd
Background: In children with anorectal malformations (ARM), additional anomalies can occur within the VACTERL-association. Routine screening is of great importance for early identification and potential treatment. However, uniformity in screening pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84d269bc910ec8db81ba9e7f72b4290c
https://pure.amc.nl/en/publications/the-importance-of-screening-for-additional-anomalies-in-patients-with-anorectal-malformations(f07edeaa-2bdc-47e2-a576-3d5f2bb154d8).html
https://pure.amc.nl/en/publications/the-importance-of-screening-for-additional-anomalies-in-patients-with-anorectal-malformations(f07edeaa-2bdc-47e2-a576-3d5f2bb154d8).html
Autor:
Luc Bruyndonckx, Eline A. Nannenberg, Saskia N. van der Crabben, Bart Straver, Marianna Bugiani, Wes Onland, Sally-Ann B. Clur, Judith L. Vogelzang, Irene M. Kuipers
Publikováno v:
American Journal of Medical Genetics. Part a
Bruyndonckx, L, Vogelzang, J L, Bugiani, M, Straver, B, Kuipers, I M, Onland, W, Nannenberg, E A, Clur, S-A & van der Crabben, S N 2021, ' Childhood onset nexilin dilated cardiomyopathy : A heterozygous and a homozygous case ', American Journal of Medical Genetics Part A, vol. 185, no. 8, pp. 2464-2470 . https://doi.org/10.1002/ajmg.a.62231
American journal of medical genetics : part A
American journal of medical genetics. Part A, 185(8), 2464-2470. Wiley-Liss Inc.
Bruyndonckx, L, Vogelzang, J L, Bugiani, M, Straver, B, Kuipers, I M, Onland, W, Nannenberg, E A, Clur, S-A & van der Crabben, S N 2021, ' Childhood onset nexilin dilated cardiomyopathy : A heterozygous and a homozygous case ', American Journal of Medical Genetics Part A, vol. 185, no. 8, pp. 2464-2470 . https://doi.org/10.1002/ajmg.a.62231
American journal of medical genetics : part A
American journal of medical genetics. Part A, 185(8), 2464-2470. Wiley-Liss Inc.
Pathogenic heterozygous NEXN variants are associated with progressive dilated cardiomyopathy (DCM) usually presenting around 50 years of age. We describe an asymptomatic boy who had transient DCM at 3 months of age, that resolved by 4 months. Present
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7bb1dfdd766a928c27f04db6a9f9c7e
https://doi.org/10.1002/ajmg.a.62231
https://doi.org/10.1002/ajmg.a.62231