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Acta Paediatrica (Oslo, Norway : 1992)|February 7, 2024
Higher risk of cerebral palsy, seizures/epilepsy, visual- and hearing impairments, cancer, injury and child abuse in children with congenital anomalies: Data from the EUROlinkCAT studyStine Kjaer Urhoj, Joan Morris, Maria Loane, et al.
European Journal of Human Genetics : EJHG|January 12, 2012
Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in EuropeDiana Wellesley, Helen Dolk, Patricia A Boyd, et al.
Pediatric Neurology|February 3, 2026
Antiseizure Prescription for Children With Severe Congenital Heart Defects and Children With Gastrointestinal AnomaliesMads Damkjaer, Joan K Morris, Elisa Ballardini, et al.
Birth Defects Research|July 26, 2023
The burden of disease for children born alive with Turner syndrome-A European cohort studyAnn-Louise Rud Andersen, Stine Kjaer Urhoj, Joachim Tan, et al.
European Journal of Human Genetics : EJHG|September 4, 2014
Meckel-Gruber Syndrome: a population-based study on prevalence, prenatal diagnosis, clinical features, and survival in EuropeIngeborg Barisic, Ljubica Boban, Maria Loane, et al.
Acta Paediatrica (Oslo, Norway : 1992)|February 24, 2023
European study showed that children with congenital anomalies often underwent multiple surgical procedures at different ages across EuropeEster Garne, Maria Loane, Joachim Tan, et al.
European Journal of Human Genetics : EJHG|January 9, 2014
Prevalence, prenatal diagnosis and clinical features of oculo-auriculo-vertebral spectrum: a registry-based study in EuropeIngeborg Barisic, Ljubica Odak, Maria Loane, et al.
Epidemiology (Cambridge, Mass.)|September 2, 2015
The Association of H1N1 Pandemic Influenza with Congenital Anomaly Prevalence in Europe: An Ecological Time Series StudyJohannes Michiel Luteijn, Marie-Claude Addor, Larraitz Arriola, et al.
Public Health Genomics|April 10, 2014
European recommendations for primary prevention of congenital anomalies: a joined effort of EUROCAT and EUROPLAN projects to facilitate inclusion of this topic in the National Rare Disease PlansDomenica Taruscio, Larraitz Arriola, Francesca Baldi, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|June 16, 2016
Use of hierarchical models to analyze European trends in congenital anomaly prevalenceAlana Cavadino, David Prieto-Merino, Marie-Claude Addor, et al.
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