Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Marry E.B. Rijlaarsdam"'
Autor:
Enrico Lopriore, Dick Oepkes, Johanna M. Middeldorp, A. K. K. Teunissen, Monique C. Haak, Marry E.B. Rijlaarsdam, E.W. van Zwet, Frans J.C.M. Klumper, L. S. T. M. Boons, A. D. J. ten Harkel, Sanne J. Eschbach
Publikováno v:
Ultrasound in Obstetrics and Gynecology, 49(6), 737-743
Objectives Severe right ventricular outflow tract obstruction (RVOTO) is a potential complication in recipient twins of twin-to-twin transfusion syndrome (TTTS) that requires postnatal follow-up or treatment. We aimed to evaluate pregnancy characteri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6dc96134cb3347bcfb457bc463e676e
https://doi.org/10.1002/uog.16008
https://doi.org/10.1002/uog.16008
Autor:
I.M. van Beynum, Ingrid M.E. Frohn-Mulder, Monique C. Haak, Martijn G. Slieker, Lukas A. J. Rammeloo, A. Reimer, Marry E.B. Rijlaarsdam, Caterina M. Bilardo, S. A. Clur, Gwendolyn T. R. Manten, N.W.E. Van Den Berg, Jérôme Cornette, Diederik R.H. de Bruijn, Matthias W. Freund, A.B.M.H. Rackowitz, K.E.H. van Loo-Maurus
Publikováno v:
Van den Berg, N W E, Slieker, M G, van Beynum, I M, Bilardoo, C M, de Bruijn, D, Clur, S A, Cornette, J M J, Frohn-Mulder, I M E, Haak, M C, van Loo-Maurus, K E H, Manten, G T R, Rackowitz, A B M H, Rammeloo, L A J, Reimer, A, Rijlaarsdam, M E B & Freund, M W 2016, ' Fluorinated steroids do not improve outcome of isolated atrioventricular block ', International Journal of Cardiology, vol. 225, pp. 167-171 . https://doi.org/10.1016/j.ijcard.2016.09.119
International Journal of Cardiology, 225, 167-171. Elsevier Ireland Ltd
International Journal of Cardiology, 225, pp. 167-171
International Journal of Cardiology, 225, 167-171
International Journal of Cardiology, 225, 167-171. ELSEVIER IRELAND LTD
International journal of cardiology, 225, 167-171. Elsevier Ireland Ltd
International Journal of Cardiology, 225, 167. Elsevier Ireland Ltd
International Journal of Cardiology, 225, 167-171. Elsevier Ireland Ltd
International Journal of Cardiology, 225, pp. 167-171
International Journal of Cardiology, 225, 167-171
International Journal of Cardiology, 225, 167-171. ELSEVIER IRELAND LTD
International journal of cardiology, 225, 167-171. Elsevier Ireland Ltd
International Journal of Cardiology, 225, 167. Elsevier Ireland Ltd
Introduction: Congenital atrioventricular block (CAVB) is a rare disorder with a significant morbidity and mortality. Consensus regarding the prescription and efficacy of prenatal corticosteroids is lacking. This nationwide study was initiated to eva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3e4ee17035e24622aba4fc6f1ae0a44
https://doi.org/10.1016/j.ijcard.2016.09.119
https://doi.org/10.1016/j.ijcard.2016.09.119
Autor:
Marry E.B. Rijlaarsdam, Jaroslav Hruda, Eva Pajkrt, Nico A. Blom, Freya Türkeri, Sally-Ann B. Clur, Caroline J. Bax, Monique C. Haak, Christianne J.M. de Groot, Christine L. van Velzen
Publikováno v:
van Velzen, C L, Turkeri, F, Pajkrt, E, Clur, S-A, Rijlaarsdam, M E B, Bax, C J, Hruda, J, de Groot, C J M, Blom, N A & Haak, M C 2016, ' Pregnancy complications in singleton pregnancies with isolated fetal heart defects ', Acta Obstetricia et Gynecologica Scandinavica, vol. 95, no. 11, pp. 1273-1280 . https://doi.org/10.1111/aogs.12955
Acta obstetricia et gynecologica Scandinavica, 95(11), 1273-1280. Wiley-Blackwell
Acta Obstetricia et Gynecologica Scandinavica, 95(11), 1273-1280
Acta Obstetricia et Gynecologica Scandinavica, 95(11), 1273-1280. Wiley-Blackwell
Acta obstetricia et gynecologica Scandinavica, 95(11), 1273-1280. Wiley-Blackwell
Acta Obstetricia et Gynecologica Scandinavica, 95(11), 1273-1280
Acta Obstetricia et Gynecologica Scandinavica, 95(11), 1273-1280. Wiley-Blackwell
Introduction As the prenatal detection rates of congenital heart defects (CHDs) increase, obstetricians are more frequently faced with pregnancies complicated by a fetal CHD. Congenital anomalies in general are associated with preterm birth and fetal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f6fd2f7cac58ce8ea17ae1053b98a76
https://doi.org/10.1111/aogs.12955
https://doi.org/10.1111/aogs.12955
Autor:
A. Kragt, Marry E.B. Rijlaarsdam, E.W. van Zwet, Eva Pajkrt, Nico A. Blom, C. L. Bax, Sally-Ann B. Clur, Fenna A. R. Jansen, C. L. van Velzen, Monique C. Haak, J.M.M. van Lith, H. R. Zuurveen
Publikováno v:
Ultrasound in Obstetrics & Gynecology. 48:357-364
Objectives Congenital heart defects (CHDs) are reported to be associated with a smaller fetal head circumference (HC) and neurodevelopmental delay. Recent studies suggest that altered intrauterine brain hemodynamics may explain these findings. Our ob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::315b393cc523ad5ae13cf806ec08e556
https://doi.org/10.1002/uog.15980
https://doi.org/10.1002/uog.15980
Autor:
S. A. Clur, Marry E.B. Rijlaarsdam, Monique C. Haak, Eva Pajkrt, Nico A. Blom, C. J. M. de Groot, Caroline J. Bax, Jaroslav Hruda, C. L. van Velzen
Publikováno v:
Ultrasound in Obstetrics and Gynecology
Objective To examine the accuracy of fetal echocardiography in diagnosing congenital heart disease (CHD) at the fetal medicine units of three tertiary care centers. Methods This was a multicenter cohort study of tertiary echocardiography referrals be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2e1165d41c3c5d25a3fa9f3023fe5c2
https://doi.org/10.1002/uog.15742
https://doi.org/10.1002/uog.15742
Autor:
Fenna A. R. Jansen, Eva Pajkrt, Stephani Klingeman Plati, Shama L. Bhola, Marion A. de Boer, Monique C. Haak, Christine L. van Velzen, Marry E.B. Rijlaarsdam, Nico A. Blom, Mariëtte J.V. Hoffer, Sally-Ann B. Clur, Alida C. Knegt
Publikováno v:
Prenatal Diagnosis. 36:177-185
Objectives To demonstrate the spectrum of copy number variants (CNVs) in fetuses with isolated left-sided congenital heart defects (CHDs), and analyse genetic content. Methods Between 2003 and 2012, 200 fetuses were identified with left-sided CHD. Ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1db4587d62e533ff371f04cd6b9f470f
https://doi.org/10.1002/pd.4767
https://doi.org/10.1002/pd.4767
Autor:
C. M. Bilardo, Jaroslav Hruda, C. L. van Velzen, Marry E.B. Rijlaarsdam, S. A. Clur, Nico A. Blom, Monique C. Haak, Eva Pajkrt, G. Reijnders, F. Galindo-Garre, C. J. M. de Groot, Caroline J. Bax
Publikováno v:
Ultrasound in Obstetrics and Gynecology, 45(3), 320-325
Ultrasound in Obstetrics & Gynecology, 45(3), 320-325. Wiley
Ultrasound in obstetrics & gynecology, 45(3), 320-325. John Wiley and Sons Ltd
van Velzen, C L, Haak, M C, Reijnders, G, Rijlaarsdam, M E B, Bax, C J, Pajkrt, E, Hruda, J, Galindo Garre, F, Bilardo, C M, de Groot, C J M, Blom, N A & Clur, S A 2015, ' Prenatal detection of transposition of the great arteries reduces mortality and morbidity ', Ultrasound in Obstetrics and Gynecology, vol. 45, no. 3, pp. 320-325 . https://doi.org/10.1002/uog.14689
Ultrasound in Obstetrics and Gynecology, 45(3), 320-325. John Wiley and Sons Ltd
Ultrasound in Obstetrics & Gynecology, 45(3), 320-325. Wiley
Ultrasound in obstetrics & gynecology, 45(3), 320-325. John Wiley and Sons Ltd
van Velzen, C L, Haak, M C, Reijnders, G, Rijlaarsdam, M E B, Bax, C J, Pajkrt, E, Hruda, J, Galindo Garre, F, Bilardo, C M, de Groot, C J M, Blom, N A & Clur, S A 2015, ' Prenatal detection of transposition of the great arteries reduces mortality and morbidity ', Ultrasound in Obstetrics and Gynecology, vol. 45, no. 3, pp. 320-325 . https://doi.org/10.1002/uog.14689
Ultrasound in Obstetrics and Gynecology, 45(3), 320-325. John Wiley and Sons Ltd
Objectives To evaluate the prenatal detection of transposition of the great arteries (TGA), after the introduction of a Dutch screening program in 2007, as well as the effect of prenatal detection on pre- and postsurgical mortality and morbidity.Meth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4e6511136d14d9d4901fcd9e420877e
https://doi.org/10.1002/uog.14689
https://doi.org/10.1002/uog.14689
Autor:
Marry E.B. Rijlaarsdam, Arno A.W. Roest, Jacob Geleijns, Mark G. Hazekamp, Lucia J.M. Kroft, Joost J. H. Roelofs
Publikováno v:
Case Reports in Pediatrics
Case Reports in Pediatrics, Vol 2013 (2013)
Case Reports in Pediatrics, Vol 2013 (2013)
We present 3 patients with 4 causes of mediastinal fluid collection after congenital cardiac surgery in this extended case report. Volumetric computed tomography played an essential role in diagnosing causes and extent, relevant to subsequent managem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5364783c6e2f77c69a39f93e19f0e78
https://doi.org/10.1155/2013/426923
https://doi.org/10.1155/2013/426923
Autor:
Dave R. Koolbergen, Eline F. Bruggemans, Mark G. Hazekamp, Marry E.B. Rijlaarsdam, Paul H. Schoof, Gerard J.F. Hoohenkerk
Publikováno v:
Annals of Thoracic Surgery, 90(5), 1554
Background. Outcome of surgical correction of atrioventricular septal defects (AVSD) still varies despite enhanced results. We reviewed our 30-year experience with AVSD repair and identified risk factors for mortality and reoperation. Methods. Betwee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac21bfb44709da9ea3e883baa4ff0b64
https://doi.org/10.1016/j.athoracsur.2010.06.008
https://doi.org/10.1016/j.athoracsur.2010.06.008
Autor:
Michel I.M. Versteegh, Marietta Swart-van den Berg, Ben C.J. Hamel, Marieke J.H. Baars, Arthur J.H.A. Scholte, Wilhelmina S. Kerstjens-Frederikse, Jacques C. Giltay, Martijn H. Breuning, Iris van der Schoot-van Velzen, Hans-Joachim Schäbitz, Yvonne Hilhorst-Hofstee, Gerard Pals, Marry E.B. Rijlaarsdam, Emilia K. Bijlsma
Publikováno v:
Human Mutation, 31, 12, pp. E915-27
Human mutation, 31(12), E1915-E1927. Wiley-Liss Inc.
Human Mutation, 31(12), E1915-E1927. Wiley
Human Mutation
Human Mutation, 31, E915-27
Human mutation, 31(12), E1915-E1927. Wiley-Liss Inc.
Human Mutation, 31(12), E1915-E1927. Wiley
Human Mutation
Human Mutation, 31, E915-27
Marfan syndrome (MFS) is a dominant disorder with a recognizable phenotype. In most patients with the classical phenotype mutations are found in the fibrillin-1 gene (FBN1) on chromosome 15q21. It is thought that most mutations act in a dominant nega
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9a8155c35b54fd38c666558d2acaba4
https://doi.org/10.1002/humu.21372
https://doi.org/10.1002/humu.21372