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Spectrum of congenital anomalies among VACTERL cases: a EUROCAT population-based study.
van de Putte, Romy; van Rooij, Iris A L M; Marcelis, Carlo L M; Guo, Michel; Brunner, Han G; Addor, Marie-Claude; Cavero-Carbonell, Clara; Dias, Carlos M; Draper, Elizabeth S; Etxebarriarteun, Larraitz; Gatt, Miriam; Haeusler, Martin; Khoshnood, Babak; Klungsoyr, Kari; Kurinczuk, Jenny J; Lanzoni, Monica; Latos-Bielenska, Anna; Luyt, Karen; O'Mahony, Mary T; Miller, Nicola; Mullaney, Carmel; Nelen, Vera; Neville, Amanda J; Perthus, Isabelle; Pierini, Anna; Randrianaivo, Hanitra; Rankin, Judith; Rissmann, Anke; Rouget, Florence; Schaub, Bruno; Tucker, David; Wellesley, Diana; Wiesel, Awi; Zymak-Zakutnia, Natalya; Loane, Maria; Barisic, Ingeborg; de Walle, Hermien E K; Roeleveld, Nel; Bergman, Jorieke E H.
Afiliación
  • van de Putte R; Department for Health Evidence, Radboud Institute for Health Sciences, Radboud University Medical Center (Radboudumc), Nijmegen, The Netherlands. Romy.vandePutte@radboudumc.nl.
  • van Rooij IALM; Department for Health Evidence, Radboud Institute for Health Sciences, Radboud University Medical Center (Radboudumc), Nijmegen, The Netherlands.
  • Marcelis CLM; Paediatric Surgery, Radboudumc Amalia Children's Hospital, Nijmegen, The Netherlands.
  • Guo M; Department of Human Genetics, Radboudumc, Nijmegen, The Netherlands.
  • Brunner HG; Department for Health Evidence, Radboud Institute for Health Sciences, Radboud University Medical Center (Radboudumc), Nijmegen, The Netherlands.
  • Addor MC; Department of Human Genetics, Radboudumc, Nijmegen, The Netherlands.
  • Cavero-Carbonell C; Department of Clinical Genetics, Maastricht University Medical Centre, Maastricht, The Netherlands.
  • Dias CM; Department of Woman-Mother-Child, University Medical Center CHUV, Lausanne, Switzerland.
  • Draper ES; Rare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region, Valencia, Spain.
  • Etxebarriarteun L; Epidemiology Department, National Institute of Health Doctor Ricardo Jorge, Lisbon, Portugal.
  • Gatt M; Department of Health Sciences, University of Leicester, Leicester, UK.
  • Haeusler M; Department of Health, Public Health Service, Basque Government Basque Country, Vitoria-Gasteiz, Spain.
  • Khoshnood B; Malta Congenital Anomalies Register, Directorate for Health Information and Research, Pietà, Malta.
  • Klungsoyr K; Department of Obstetrics and Gynecology, Medical University of Graz, Graz, Austria.
  • Kurinczuk JJ; INSERM UMR 1153, Obstetrical, Perinatal and Pediatric Epidemiology Research Team (EPOPé), Center of Research in Epidemiology and Statistics Sorbonne Paris Cité (CRESS), DHU Risks in Pregnancy, Paris Descartes University, Paris, France.
  • Lanzoni M; Department of Global Public Health and Primary Care, Division for Mental and Physical Health, Norwegian Institute of Public Health, University of Bergen, Bergen, Norway.
  • Latos-Bielenska A; National Perinatal Epidemiology Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK.
  • Luyt K; European Commission, Joint Research Centre (JRC), Ispra, Italy.
  • O'Mahony MT; Department of Medical Genetics, Poznan University of Medical Sciences, Poznan, Poland.
  • Miller N; South West Congenital Anomaly Register (SWCAR), Bristol Medical School, University of Bristol, Bristol, UK.
  • Mullaney C; Department of Public Health, Health Service Executive - South, Cork, Ireland.
  • Nelen V; National Congenital Anomaly and Rare Disease Registration Service, Public Health England, Newcastle upon Tyne, UK.
  • Neville AJ; Department of Public Health, HSE South East, Lacken, Kilkenny, Ireland.
  • Perthus I; Provinciaal Instituut voor Hygiene (PIH), Antwerp, Belgium.
  • Pierini A; Registro IMER - IMER Registry (Emila Romagna Registry of Birth Defects), Center for Clinical and Epidemiological Research, University of Ferrara, Azienda Ospedaliero-Universitaria di Ferrara, Ferrara, Italy.
  • Randrianaivo H; Auvergne registry of congenital anomalies (CEMC-Auvergne), Department of clinical genetics, Centre de Référence des Maladies Rares, University Hospital of Clermont-Ferrand, Clermont-Ferrand, France.
  • Rankin J; Tuscany Registry of Congenital Defects (TRDC), Institute of Clinical Physiology - National Research Council/Fondazione Toscana Gabriele Monasterio, Pisa, Italy.
  • Rissmann A; Register of Congenital Malformations of Reunion Island, CHU Réunion, St Pierre, France.
  • Rouget F; Institute of Health and Society, Newcastle University, Newcastle, UK.
  • Schaub B; Malformation Monitoring Centre Saxony-Anhalt, Medical Faculty Otto-von-Guericke University, Magdeburg, Germany.
  • Tucker D; Brittany Registry of Congenital Anomalies, CHU Rennes, Inserm, EHESP, Irset (Institut de recherche en santé, environnement et travail), University Rennes, Rennes, France.
  • Wellesley D; French West Indies Registry, Registre des Malformations des Antilles (REMALAN), Maison de la Femme de la Mère et de l'Enfant, University Hospital of Martinique, Fort-de-France, France.
  • Wiesel A; CARIS, Public Health Wales, Singleton Hospital, Swansea, Wales, UK.
  • Zymak-Zakutnia N; Wessex Clinical Genetics Department, Princess Anne Hospital, Southampton, UK.
  • Loane M; Department of Pediatrics, Birth Registry Mainz Model, University Medical Center of Mainz, Mainz, Germany.
  • Barisic I; OMNI-Net Ukraine Birth Defects Program and Khmelnytsky City Children's Hospital, Khmelnytsky, Ukraine.
  • de Walle HEK; Centre for Maternal, Fetal and lnfant Research, lnstitute of Nursing and Health Research, Ulster University, Belfast, Northern lreland, UK.
  • Roeleveld N; Centre of Excellence for Reproductive and Regenerative Medicine, Children's Hospital Zagreb, Medical School University of Zagreb, Zagreb, Croatia.
  • Bergman JEH; University of Groningen, University Medical Center Groningen, Department of Genetics, EUROCAT Northern Netherlands, Groningen, The Netherlands.
Pediatr Res ; 87(3): 541-549, 2020 02.
Article en En | MEDLINE | ID: mdl-31499513
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Canal Anal / Columna Vertebral / Tráquea / Deformidades Congénitas de las Extremidades / Esófago / Cardiopatías Congénitas / Riñón Tipo de estudio: Clinical_trials / Guideline / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Humans País/Región como asunto: Europa Idioma: En Revista: Pediatr Res Año: 2020 Tipo del documento: Article País de afiliación: Países Bajos
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Canal Anal / Columna Vertebral / Tráquea / Deformidades Congénitas de las Extremidades / Esófago / Cardiopatías Congénitas / Riñón Tipo de estudio: Clinical_trials / Guideline / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Humans País/Región como asunto: Europa Idioma: En Revista: Pediatr Res Año: 2020 Tipo del documento: Article País de afiliación: Países Bajos