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Luc De Catte

Showing results (31-40 of 95) with videos related to

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Prenatal Diagnosis|April 18, 2012
Effects of chemotherapy during pregnancy on the maternal and fetal heartMina Mhallem Gziri, Frédéric Amant, Frédéric Debiève, et al.
Prenatal Diagnosis|April 9, 2008
First trimester prenatal diagnosis of 13q-syndrome presenting with increased nuchal translucency, Dandy-Walker malformation and small parietal encephalocoeleAn Hindryckx, Luc De Catte, Hilde Van Esch, et al.
Prenatal Diagnosis|March 5, 2013
A morphometric study of the human fetal heart on post-mortem 3-tesla magnetic resonance imagingInga Sandaite, Luc De Catte, Philippe Moerman, et al.
Seminars in Immunopathology|August 14, 2020
Foetal therapies and their influence on preterm birthIgnacio Valenzuela, Johannes van der Merwe, Luc De Catte, et al.
Fetal Diagnosis and Therapy|October 16, 2007
Chorionic membrane separation following fetoscopy. A role for collagen plugging of the fetoscopic access site? Commentary on Chang et al: Transient chorioamniotic membrane separation after fetoscope guide laser therapy for twin-twin transfusion syndrome: a case report (Fetal Diagn Ther 2007;22:180-182)Roland Devlieger, Tim Van Mieghem, Liesbeth Lewi, et al.
Prenatal Diagnosis|March 8, 2019
Placental vascular recruitment after single intrauterine demise: A newly diagnosed phenomenon unique to monochorionic pregnanciesSanne Deneckere, Isabel Couck, Roland Devlieger, et al.
European Journal of Medical Genetics|May 24, 2014
Exome sequencing identifies a recessive PIGN splice site mutation as a cause of syndromic congenital diaphragmatic herniaP D Brady, Philippe Moerman, Luc De Catte, et al.
Prenatal Diagnosis|June 21, 2018
Proposal for standardized prenatal ultrasound assessment of the fetus with congenital diaphragmatic hernia by the European reference network on rare inherited and congenital anomalies (ERNICA)Francesca Maria Russo, Anne-Gael Cordier, Luc De Catte, et al.
Fetal Diagnosis and Therapy|June 12, 2013
Postmortem high-resolution fetal magnetic resonance imaging in three cases of lower urinary tract obstructionMathieu Lefere, Inga Sandaite, An Hindryckx, et al.
Best Practice & Research. Clinical Obstetrics & Gynaecology|June 12, 2012
Minimally invasive fetal therapyTim van Mieghem, David Baud, Roland Devlieger, et al.
Pageof 10

Showing results (31-40 of 95) with videos related to

Sort By:
Pageof 10
Prenatal Diagnosis|April 18, 2012
Effects of chemotherapy during pregnancy on the maternal and fetal heartMina Mhallem Gziri, Frédéric Amant, Frédéric Debiève, et al.
Prenatal Diagnosis|April 9, 2008
First trimester prenatal diagnosis of 13q-syndrome presenting with increased nuchal translucency, Dandy-Walker malformation and small parietal encephalocoeleAn Hindryckx, Luc De Catte, Hilde Van Esch, et al.
Prenatal Diagnosis|March 5, 2013
A morphometric study of the human fetal heart on post-mortem 3-tesla magnetic resonance imagingInga Sandaite, Luc De Catte, Philippe Moerman, et al.
Seminars in Immunopathology|August 14, 2020
Foetal therapies and their influence on preterm birthIgnacio Valenzuela, Johannes van der Merwe, Luc De Catte, et al.
Fetal Diagnosis and Therapy|October 16, 2007
Chorionic membrane separation following fetoscopy. A role for collagen plugging of the fetoscopic access site? Commentary on Chang et al: Transient chorioamniotic membrane separation after fetoscope guide laser therapy for twin-twin transfusion syndrome: a case report (Fetal Diagn Ther 2007;22:180-182)Roland Devlieger, Tim Van Mieghem, Liesbeth Lewi, et al.
Prenatal Diagnosis|March 8, 2019
Placental vascular recruitment after single intrauterine demise: A newly diagnosed phenomenon unique to monochorionic pregnanciesSanne Deneckere, Isabel Couck, Roland Devlieger, et al.
European Journal of Medical Genetics|May 24, 2014
Exome sequencing identifies a recessive PIGN splice site mutation as a cause of syndromic congenital diaphragmatic herniaP D Brady, Philippe Moerman, Luc De Catte, et al.
Prenatal Diagnosis|June 21, 2018
Proposal for standardized prenatal ultrasound assessment of the fetus with congenital diaphragmatic hernia by the European reference network on rare inherited and congenital anomalies (ERNICA)Francesca Maria Russo, Anne-Gael Cordier, Luc De Catte, et al.
Fetal Diagnosis and Therapy|June 12, 2013
Postmortem high-resolution fetal magnetic resonance imaging in three cases of lower urinary tract obstructionMathieu Lefere, Inga Sandaite, An Hindryckx, et al.
Best Practice & Research. Clinical Obstetrics & Gynaecology|June 12, 2012
Minimally invasive fetal therapyTim van Mieghem, David Baud, Roland Devlieger, et al.
Pageof 10