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Ester Garne

Showing results (61-70 of 172) with videos related to

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Cardiology in the Young|January 19, 2013
Cancer risk among patients with congenital heart defects: a nationwide follow-up studyMorten Olsen, Ester Garne, Claus Sværke, et al.
Frontiers in Pediatrics|December 16, 2021
The Voice of Parents of Children With a Congenital Anomaly - A EUROlinkCAT StudyKristina Garne Holm, Amanda Julie Neville, Anna Pierini, et al.
Cardiology in the Young|November 28, 2012
Atrioventricular septal defects among infants in Europe: a population-based study of prevalence, associated anomalies, and survivalNikolas Christensen, Helle Andersen, Ester Garne, et al.
Public Health Genomics|March 21, 2015
Primary prevention of congenital anomalies: recommendable, feasible and achievableDomenica Taruscio, Alberto Mantovani, Pietro Carbone, et al.
European Journal of Public Health|August 18, 2023
Educational achievement of children with selected major congenital anomalies and associated factors: a Finnish registry-based studyZahra Roustaei, Anna Heino, Sonja Kiuru-Kuhlefelt, et al.
Birth Defects Research|December 27, 2022
The quality and the accuracy of codes for terminations of pregnancy for fetal anomalies recorded in hospital databases in three countries in northern EuropeEster Garne, Stine Kjaer Urhoj, Marian Bakker, et al.
The New England Journal of Medicine|June 19, 2010
Valproic acid monotherapy in pregnancy and major congenital malformationsJanneke Jentink, Maria A Loane, Helen Dolk, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|November 4, 2014
Effect of consanguinity on birth defects in Saudi women: results from a nested case-control studyMuhammad Ali Majeed-Saidan, Amer N Ammari, Amal M AlHashem, et al.
European Journal of Pediatrics|June 10, 2025
Morbidity in children with major kidney anomalies: a European population-based studyEster Garne, Mads Damkjær, Anke Rissmann, et al.
European Journal of Medical Genetics|March 30, 2018
A sustainable solution for the activities of the European network for surveillance of congenital anomalies: EUROCAT as part of the EU Platform on Rare Diseases RegistrationAgnieszka Kinsner-Ovaskainen, Monica Lanzoni, Ester Garne, et al.
Pageof 18

Showing results (61-70 of 172) with videos related to

Sort By:
Pageof 18
Cardiology in the Young|January 19, 2013
Cancer risk among patients with congenital heart defects: a nationwide follow-up studyMorten Olsen, Ester Garne, Claus Sværke, et al.
Frontiers in Pediatrics|December 16, 2021
The Voice of Parents of Children With a Congenital Anomaly - A EUROlinkCAT StudyKristina Garne Holm, Amanda Julie Neville, Anna Pierini, et al.
Cardiology in the Young|November 28, 2012
Atrioventricular septal defects among infants in Europe: a population-based study of prevalence, associated anomalies, and survivalNikolas Christensen, Helle Andersen, Ester Garne, et al.
Public Health Genomics|March 21, 2015
Primary prevention of congenital anomalies: recommendable, feasible and achievableDomenica Taruscio, Alberto Mantovani, Pietro Carbone, et al.
European Journal of Public Health|August 18, 2023
Educational achievement of children with selected major congenital anomalies and associated factors: a Finnish registry-based studyZahra Roustaei, Anna Heino, Sonja Kiuru-Kuhlefelt, et al.
Birth Defects Research|December 27, 2022
The quality and the accuracy of codes for terminations of pregnancy for fetal anomalies recorded in hospital databases in three countries in northern EuropeEster Garne, Stine Kjaer Urhoj, Marian Bakker, et al.
The New England Journal of Medicine|June 19, 2010
Valproic acid monotherapy in pregnancy and major congenital malformationsJanneke Jentink, Maria A Loane, Helen Dolk, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|November 4, 2014
Effect of consanguinity on birth defects in Saudi women: results from a nested case-control studyMuhammad Ali Majeed-Saidan, Amer N Ammari, Amal M AlHashem, et al.
European Journal of Pediatrics|June 10, 2025
Morbidity in children with major kidney anomalies: a European population-based studyEster Garne, Mads Damkjær, Anke Rissmann, et al.
European Journal of Medical Genetics|March 30, 2018
A sustainable solution for the activities of the European network for surveillance of congenital anomalies: EUROCAT as part of the EU Platform on Rare Diseases RegistrationAgnieszka Kinsner-Ovaskainen, Monica Lanzoni, Ester Garne, et al.
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