Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Jacoba Louw"'
Autor:
Ruth Heying, Bartosz Ditkowski, Bjorn Cools, Stefan Frerich, Derize Boshoff, Jelena Hubrechts, Marc Gewillig, Bart Meyns, Jacoba Louw, Benedicte Eyskens, Thierry Sluysmans, Daniël De Wolf, Werner Budts, Filip Rega, D. Bos
Publikováno v:
INTERNATIONAL JOURNAL OF CARDIOLOGY
International Journal of Cardiology, 323, 40-46. Elsevier Ireland Ltd
International journal of cardiology, Vol. 323, no.323, p. 40-46 (2021)
International Journal of Cardiology, 323, 40-46. Elsevier Ireland Ltd
International journal of cardiology, Vol. 323, no.323, p. 40-46 (2021)
AIMS: Percutaneous pulmonary valve implantation (PPVI) has proven good hemodynamic results. As infective endocarditis (IE) remains a potential complication with limited available clinical data, we reviewed our patient records to improve future strate
Autor:
Bjorn Cools, Geert Maleux, Jelena Hubrechts, Marc Gewillig, Ruth Heying, Jacoba Louw, Emma Storme, Sofie Malekzadeh‐Milanii, Stephen C. Brown, Derize Boshoff, Stefan Frerich
Publikováno v:
Catheterization and Cardiovascular interventions, 94(7), 996-1002. Wiley
Background To determine the feasibility and clinical result of selective embolization of hepatoduodenal or paratracheal lymphatics in Fontan patients with protein-losing enteropathy (PLE) or plastic bronchitis (PB). Methods Dilated lymph vessels in p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::170c942ee45247200a23e423a9305ba4
https://cris.maastrichtuniversity.nl/en/publications/f7a1a744-e605-4f3a-957a-4fc2554c2deb
https://cris.maastrichtuniversity.nl/en/publications/f7a1a744-e605-4f3a-957a-4fc2554c2deb
Autor:
Stefan Frerich, Derize Boshoff, Marc Gewillig, Jelte Kelchtermans, Tiago Rafael Veloso, Bart Meyns, Benedicte Eyskens, Bjorn Cools, Jacoba Louw, Mieke Roggen, Jorien Claes, Filip Rega, Lorenz Grossar, Ruth Heying, Bartosz Ditkowski
Publikováno v:
The Pediatric infectious disease journal. 38(5)
BACKGROUND: Infective endocarditis (IE) remains a diagnostic and therapeutic challenge associated with high morbidity and mortality. We evaluated the microbial profile and clinical manifestation of IE in children. METHODS: A retrospective study exami
The diagnostic value of next generation sequencing in familial nonsyndromic congenital heart defects
Autor:
Jeroen Breckpot, Yaojuan Jia, Jacoba Louw, Luc Dehaspe, Yves Sznajer, Catherine Barrea, Koenraad Devriendt, Anniek Corveleyn, Diether Lambrechts, Marc Gewillig, Erika Souche, Joris Vermeesch, Bert Callewaert
Publikováno v:
American Journal of Medical Genetics Part A. 167:1822-1829
To determine the diagnostic value of massive parallel sequencing of a panel of known cardiac genes in familial nonsyndromic congenital heart defects (CHD), targeted sequencing of the coding regions of 57 genes previously implicated in CHD was perform
Publikováno v:
American Journal of Medical Genetics Part A. 167:1142-1146
MEIS2 has been associated with cleft palate and cardiac septal defects as well as varying degrees of intellectual disability. We present a female patient with a more severe phenotype compared to previous reported patients. She has multiple congenital
Autor:
Benedicte Eyskens, Karel Allegaert, Ruth Heying, Marc Gewillig, Liesbeth Thewissen, Bjorn Cools, Jacoba Louw, Stephen C. Brown, Elena Levtchenko, Anne Smits
Publikováno v:
Cardiovascular Journal Of Africa. 24:72-75
Objective : Circulatory failure due to acute arterial hypertension in the neonatal period is rare. This study was undertaken to assess the clinical and echocardiographic manifestations of circulatory failure resulting from acute neonatal hypertensive
Autor:
Marc Gewillig, Jacoba Louw
Publikováno v:
Current Pediatrics Reports. 1:69-74
The Fontan circulation is used as palliative surgery in the functionally univentricular heart. Due to the advances made in prenatal diagnosis, cardiac surgery, technology, and monitoring in complex congenital heart disease, survival rates have improv
Autor:
Elena Prigmore, Christopher Thornborough, Judith A. Goodship, Koenraad Devriendt, Matthew E. Hurles, Siddharth Banka, Hashim Abdul-Khaliq, Carmel Moore, Denise Williams, Seham Osman Omer, Soo-Mi Park, Diana Rajan, Okan Toka, Ganesh J. Swaminathan, Jeffrey C. Barrett, Martin O. Pollard, Frances A. Bu'Lock, Allan Daly, Anne-Karin Kahlert, Tessa Homfray, Shoumo Bhattacharya, Catherine Cosgrove, Irina-Gabriela Colgiu, Tarjinder Singh, Ingo Daehnert, Karen P. McCarthy, Michael Parker, Brigitte Stiller, Jeroen Breckpot, U.M.M. Bauer, Anna Wilsdon, Kay Metcalfe, Dorin Manase, Ami Ketley, David R. FitzPatrick, Bernard Thienpont, Katherine Lachlan, Jeremy F. McRae, Kirstin Hoff, Helen V. Firth, Marc Gewillig, Sabine Klaassen, Seema Mital, Alan Fryer, Jennifer G. Sambrook, Kerry Setchfield, Willem H. Ouwehand, Hans-Heiner Kramer, Michael Wright, Saeed Al Turki, Jacoba Louw, Bernard Keavney, AK Lampe, Hugh Watkins, Natalie Canham, Jamie Bentham, Riyadh M. Abu-Sulaiman, Ashok Kumar Manickara, Thomas Pickardt, Alejandro Sifrim, David J. Roberts, J. David Brook, Ruth Newbury-Ecob, John Danesh, Caroline F. Wright, Leema Robert, Marc-Phillip Hitz, Felix Berger, Piers E.F. Daubeney, Emma Hobson, Tomas W Fitzgerald, Helen Cox
Publikováno v:
Nature genetics
Sifrim, A, Hitz, M-P, Wilsdon, A, Breckpot, J, Turki, S H A, Thienpont, B, McRae, J, Fitzgerald, T W, Singh, T, Swaminathan, G J, Prigmore, E, Rajan, D, Abdul-Khaliq, H, Banka, S, Bauer, U M M, Bentham, J, Berger, F, Bhattacharya, S, Bu'Lock, F, Canham, N, Colgiu, I-G, Cosgrove, C, Cox, H, Daehnert, I, Daly, A, Danesh, J, Fryer, A, Gewillig, M, Hobson, E, Hoff, K, Homfray, T, Kahlert, A-K, Ketley, A, Kramer, H-H, Lachlan, K, Lampe, A K, Louw, J J, Manickara, A K, Manase, D, McCarthy, K P, Metcalfe, K, Moore, C, Newbury-Ecob, R, Omer, S O, Ouwehand, W H, Park, S-M, Parker, M J, Pickardt, T & Pollard, M O & FitzPatrick, D R 2016, ' Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing ', Nature Genetics, vol. 48, no. 9, pp. 1060-5 . https://doi.org/10.1038/ng.3627
Sifrim, A, Hitz, M-P, Wilsdon, A, Breckpot, J, Turki, S H A, Thienpont, B, McRae, J, Fitzgerald, T W, Singh, T, Swaminathan, G J, Prigmore, E, Rajan, D, Abdul-Khaliq, H, Banka, S, Bauer, U M M, Bentham, J, Berger, F, Bhattacharya, S, Bu'Lock, F, Canham, N, Colgiu, I-G, Cosgrove, C, Cox, H, Daehnert, I, Daly, A, Danesh, J, Fryer, A, Gewillig, M, Hobson, E, Hoff, K, Homfray, T, Kahlert, A-K, Ketley, A, Kramer, H-H, Lachlan, K, Lampe, A K, Louw, J J, Manickara, A K, Manase, D, McCarthy, K P, Metcalfe, K, Moore, C, Newbury-Ecob, R, Omer, S O, Ouwehand, W H, Park, S-M, Parker, M J, Pickardt, T, Pollard, M O, Keavney, B & INTERVAL Study 2016, ' Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing ', Nature Genetics, vol. 48, no. 9, pp. 1060-5 . https://doi.org/10.1038/ng.3627
Sifrim, A, Hitz, M-P, Wilsdon, A, Breckpot, J, Turki, S H A, Thienpont, B, McRae, J, Fitzgerald, T W, Singh, T, Swaminathan, G J, Prigmore, E, Rajan, D, Abdul-Khaliq, H, Banka, S, Bauer, U M M, Bentham, J, Berger, F, Bhattacharya, S, Bu'Lock, F, Canham, N, Colgiu, I-G, Cosgrove, C, Cox, H, Daehnert, I, Daly, A, Danesh, J, Fryer, A, Gewillig, M, Hobson, E, Hoff, K, Homfray, T, Kahlert, A-K, Ketley, A, Kramer, H-H, Lachlan, K, Lampe, A K, Louw, J J, Manickara, A K, Manase, D, McCarthy, K P, Metcalfe, K, Moore, C, Newbury-Ecob, R, Omer, S O, Ouwehand, W H, Park, S-M, Parker, M J, Pickardt, T & Pollard, M O & FitzPatrick, D R 2016, ' Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing ', Nature Genetics, vol. 48, no. 9, pp. 1060-5 . https://doi.org/10.1038/ng.3627
Sifrim, A, Hitz, M-P, Wilsdon, A, Breckpot, J, Turki, S H A, Thienpont, B, McRae, J, Fitzgerald, T W, Singh, T, Swaminathan, G J, Prigmore, E, Rajan, D, Abdul-Khaliq, H, Banka, S, Bauer, U M M, Bentham, J, Berger, F, Bhattacharya, S, Bu'Lock, F, Canham, N, Colgiu, I-G, Cosgrove, C, Cox, H, Daehnert, I, Daly, A, Danesh, J, Fryer, A, Gewillig, M, Hobson, E, Hoff, K, Homfray, T, Kahlert, A-K, Ketley, A, Kramer, H-H, Lachlan, K, Lampe, A K, Louw, J J, Manickara, A K, Manase, D, McCarthy, K P, Metcalfe, K, Moore, C, Newbury-Ecob, R, Omer, S O, Ouwehand, W H, Park, S-M, Parker, M J, Pickardt, T, Pollard, M O, Keavney, B & INTERVAL Study 2016, ' Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing ', Nature Genetics, vol. 48, no. 9, pp. 1060-5 . https://doi.org/10.1038/ng.3627
Congenital heart defects (CHDs) have a neonatal incidence of 0.8–1% (refs. 1,2). Despite abundant examples of monogenic CHD in humans and mice, CHD has a low absolute sibling recurrence risk (~2.7%)3, suggesting a considerable role for de novo muta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::782b7f587857178543be7ffb8892afae
Autor:
Yaojuan Jia, S Iqbal, Anniek Corveleyn, Jacoba Louw, Koenraad Devriendt, Hilde Peeters, Philippe Moerman, Marc Gewillig, Derize Boshoff
Publikováno v:
European journal of medical genetics. 57(9)
Background Two siblings from consanguineous parents of Turkish descent presented with isolated dilated cardiomyopathy, leading to early death in infancy. The diagnosis of mitogenic cardiomyopathy was made histologically. Methods and results Linkage a
Autor:
Ward Y. Vanagt, Stefan Frerich, Benedicte Eyskens, Werner Budts, Derize Boshoff, Bjorn Cools, Marc Gewillig, Els Troost, Ruth Heying, Jacoba Louw
Publikováno v:
International Journal of Cardiology, 175(1), 102-107. Elsevier Ireland Ltd
Background: Controversy remains regarding the use of covered stents in congenital heart disease (CHD). We evaluate the possibilities and safety of covered Cheatham-Platinum (CCP) stents in CHD. Methods: Single-center retrospective CHD-database study