Zobrazeno 1 - 10
of 127
pro vyhledávání: '"Luc de Catte"'
Autor:
Gunnar Naulaers, Bart De Keersmaecker, Luc De Catte, Katrien Lagrou, Sanne Vanwinkel, Katrien Jansen
Publikováno v:
BMJ Paediatrics Open, Vol 8, Iss 1 (2024)
Objective To document the course of neonatal and short-term outcomes in pregnancies after first trimester CMV (cytomegalovirus) seroconversion and negative amniotic fluid (AF) CMV PCR.Methods We included 375 patients with a first-trimester CMV seroco
Externí odkaz:
https://doaj.org/article/cd9b8d5936ca4a14933f0f66a0072ba8
Publikováno v:
BMC Pediatrics, Vol 22, Iss 1, Pp 1-8 (2022)
Abstract Background Congenital cytomegalovirus infection (cCMV) is the most common known viral cause of neurodevelopmental delay in children. The risk of severe cerebral abnormalities and neurological sequelae is greatest when the infection occurs du
Externí odkaz:
https://doaj.org/article/c3a8b7a576cc44b1b5e7e8623010e8ca
Autor:
Peter Janssens, Jean-Paul Decuypere, Stéphanie De Rechter, Luc Breysem, Dorien Van Giel, Jaak Billen, An Hindryckx, Luc De Catte, Marcella Baldewijns, Kathleen B.M. Claes, Karl M. Wissing, Koen Devriendt, Bert Bammens, Isabelle Meyts, Vicente E. Torres, Rudi Vennekens, Djalila Mekahli
Publikováno v:
Kidney International Reports, Vol 6, Iss 6, Pp 1687-1698 (2021)
Introduction: Autosomal dominant polycystic kidney disease (ADPKD) causes kidney failure typically in adulthood, but the disease starts in utero. Copeptin, epidermal growth factor (EGF), and monocyte chemoattractant protein-1 (MCP-1) are associated w
Externí odkaz:
https://doaj.org/article/ef2893b628a349dbbf02ab11b7ecada7
Autor:
Maxime Van Houdt, MD, Johannes van der Merwe, MD, PhD, Marc Gewillig, MD, PhD, Luc De Catte, MD, PhD
Publikováno v:
Radiology Case Reports, Vol 16, Iss 5, Pp 1173-1178 (2021)
We present a case of isolated intrahepatic portosystemic shunts with an aorto- hepatic-umbilical connection; prenatally diagnosed with 3D Doppler flow in a 27-year-old patient at 27 weeks of gestation. Fetal karyotyping was normal, detailed evaluatio
Externí odkaz:
https://doaj.org/article/07a920eedf5a4b288a1d26fe88544579
Autor:
Jotte Rodrigues Bento, Candice Feben, Marlies Kempers, Maartje vanRij, Mallory Woiski, Koenraad Devriendt, Luc De Catte, Marcella Baldewijns, Maaike Alaerts, Josephina Meester, Aline Verstraeten, Willy Hendson, Bart Loeys
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 10, Pp n/a-n/a (2021)
Abstract Background KCNMA1 mutations have recently been associated with a wide range of dysmorphological, gastro‐intestinal, cardiovascular, and neurological manifestations. Methods Whole exome sequencing was performed in order to identify the unde
Externí odkaz:
https://doaj.org/article/0ca074ff445a4ee0bbde97fd27f87418
Publikováno v:
Journal of the Belgian Society of Radiology, Vol 104, Iss 1 (2020)
Teaching Point: Postmortem magnetic resonance imaging can replace conventional autopsy and help diagnosis in combination with other postmortem investigations (e.g. microscopic examination of the placenta, genetic testing, etc.) under the umbrella of
Externí odkaz:
https://doaj.org/article/dc81050ac09243d28c54fee868d74465
Autor:
Laure Dombrecht, Kim Beernaert, Ellen Roets, Kenneth Chambaere, Filip Cools, Linde Goossens, Gunnar Naulaers, Luc De Catte, Joachim Cohen, Luc Deliens, on behalf of the NICU consortium
Publikováno v:
BMC Pediatrics, Vol 18, Iss 1, Pp 1-9 (2018)
Abstract Background The death of a child before or shortly after birth is frequently preceded by an end-of-life decision (ELD). Population-based studies of incidence and characteristics of ELDs in neonates and infants are rare, and those in the foeta
Externí odkaz:
https://doaj.org/article/812a8821163c42c49485a54c699746f4
Autor:
Maciej Słodki, Katarzyna-Zych-Krekora, Roland Axt-Fliedner, Ana Bianchi, Edward Araujo Junior, Isaac Blickstein, Sefa Kelekci, Lami Yeo, Jay D. Pruetz, Giuseppe Rizzo, Neil Seligman, Mark Sklansky, Luc de Catte, Stuart Weiner, Frank Chervenak, Jader Cruz, Andrii Kurkevych, Michał Krekora, Maria Respondek-Liberska
Publikováno v:
Journal of Ultrasonography, Vol 16, Iss 64, Pp 94-96 (2016)
Congenital heart defects are among the most common congenital defects and contribute substantially to the mortality of newborns and young infants, in spite of well-developed medical and surgical treatments.
Externí odkaz:
https://doaj.org/article/ae5bae1edb03430eb48299cf2aba2831
Autor:
Ellen Roets, Kim Beernaert, Kenneth Chambaere, Luc Deliens, Kim van Berkel, Luc De Catte, Sophie Vanhaesebrouck, Kristien Roelens, Laure Dombrecht
Objective: Congenital malformations are frequently diagnosed prenatally even at a viable stage. No adequate registration of incidence and characteristics of late termination of pregnancy (TOP) or abortion for medical reasons exists in Flanders. Metho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45416f6e06fd7a22a9604ee9fe6fa5ff
https://hdl.handle.net/20.500.14017/c4605c83-f72a-485d-a643-f03e055a3b4e
https://hdl.handle.net/20.500.14017/c4605c83-f72a-485d-a643-f03e055a3b4e
Autor:
Kobe Haenen, Simen Vergote, Yada Kunpalin, Luc De Catte, Roland Devlieger, Liesbeth Lewi, Johannes Van der Merwe, Francesca Russo, Philippe De Vloo, Lore Lannoo, Jan Deprest
Objective: To determine the long-term maternal impact of open fetal spina bifida repair. Design: Prospective cohort study. Setting: University Hospitals Leuven, Belgium. Population: Hundred consecutive mothers who had open maternal-fetal spina bifida
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f590bb3f5453bf6ea4213f13795d8f1b
https://doi.org/10.22541/au.167845082.26979512/v1
https://doi.org/10.22541/au.167845082.26979512/v1