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Prevalence of vascular disruption anomalies and association with young maternal age: A EUROCAT study to compare the United Kingdom with other European countries.
Morris, Joan K; Wellesley, Diana; Limb, Elizabeth; Bergman, Jorieke E H; Kinsner-Ovaskainen, Agnieszka; Addor, Marie Claude; Broughan, Jennifer M; Cavero-Carbonell, Clara; Dias, Carlos M; Echevarría-González-de-Garibay, Luis-Javier; Gatt, Miriam; Haeusler, Martin; Barisic, Ingeborg; Klungsoyr, Kari; Lelong, Nathalie; Materna-Kiryluk, Anna; Neville, Amanda; Nelen, Vera; O'Mahony, Mary T; Perthus, Isabelle; Pierini, Anna; Rankin, Judith; Rissmann, Anke; Rouget, Florence; Sayers, Geraldine; Stevens, Sarah; Tucker, David; Garne, Ester.
Afiliação
  • Morris JK; St George's, University of London, London, United Kingdom.
  • Wellesley D; Clinical Genetics, University of Southampton and Wessex Clinical Genetics Service, Princess Anne Hospital, Southampton, United Kingdom.
  • Limb E; St George's, University of London, London, United Kingdom.
  • Bergman JEH; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.
  • Kinsner-Ovaskainen A; European Commission, Joint Research Centre (JRC), Ispra, Italy.
  • Addor MC; Department of Woman-Mother-Child, University Medical Center CHUV, Lausanne, Switzerland.
  • Broughan JM; National Disease Registration Service, NHS Digital, Leeds, United Kingdom.
  • Cavero-Carbonell C; Rare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region, Valencia, Spain.
  • Dias CM; Department of Epidemiology, Instituto Nacional de Saúde Doutor Ricardo Jorge; Av padre Cruz, Lisbon, Portugal.
  • Echevarría-González-de-Garibay LJ; Ministry of Health of the Basque Government, Directorate for Healthcare Planning, Organisation and Evaluation, Vitoria-Gasteiz, Spain.
  • Gatt M; Directorate for Health Information and Research, Malta Congenital Anomalies Registry, G'Mangia, Malta.
  • Haeusler M; Medical University of Graz, Austria.
  • Barisic I; Children's Hospital Zagreb, Centre of Excellence for Reproductive and Regenerative Medicine, Medical School University of Zagreb, Zagreb, Croatia.
  • Klungsoyr K; Department of Global Public Health and Primary Care, University of Bergen, Bergen, Norway.
  • Lelong N; Division of Mental and Physical Health, Norwegian Institute of Public Health, Bergen, Norway.
  • Materna-Kiryluk A; Université de Paris, INSERM U1153, CRESS, Obstetrical Perinatal and Pediatric Epidemiology Research Team (EPOPé), Paris, France.
  • Neville A; Polish Registry of Congenital Malformations, Department of Medical Genetics, Poznan University of Medical Sciences, Poznan, Poland.
  • Nelen V; Center for Clinical and Epidemiological Research, University of Ferrara, Ferrara, Italy.
  • O'Mahony MT; Provincial Institute for Hygiene, Antwerp, Belgium.
  • Perthus I; Department of Public Health, Health Service Executive-South, Cork, Ireland.
  • Pierini A; Auvergne Registry of Congenital Anomalies (CEMC-Auvergne), Department of Clinical Genetics, Centre de Référence des Maladies Rares, University Hospital of Clermont-Ferrand, CNRS-UMR 6602, Institut Pascal, Axe TGI, équipe PEPRADE, Clermont-Ferrand, France.
  • Rankin J; Unit of Epidemiology of Rare Diseases and Congenital Anomalies, Institute of Clinical Physiology, National Research Council, Pisa, Italy.
  • Rissmann A; Fondazione Toscana Gabriele Monasterio, Pisa, Italy.
  • Rouget F; Population Health Sciences Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom.
  • Sayers G; Malformation Monitoring Centre Saxony-Anhalt, Medical Faculty Otto-von-Guericke-University Magdeburg, Magdeburg, Germany.
  • Stevens S; Brittany Registry of Congenital Anomalies, CHU Rennes, Univ Rennes, Inserm, EHESP, Irset (Institut de recherche en santé, environnement et travail) - UMR_S 1085, Rennes, France.
  • Tucker D; Health Intelligence, Research and Development Health Service Executive, Dublin, Ireland.
  • Garne E; National Disease Registration Service, NHS Digital, Leeds, United Kingdom.
Birth Defects Res ; 114(20): 1417-1426, 2022 12 01.
Article em En | MEDLINE | ID: mdl-36369770
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anormalidades Cardiovasculares / Gastrosquise / Malformações Vasculares Tipo de estudo: Etiology_studies / Prevalence_studies / Risk_factors_studies Limite: Female / Humans / Pregnancy País/Região como assunto: Europa Idioma: En Revista: Birth Defects Res Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anormalidades Cardiovasculares / Gastrosquise / Malformações Vasculares Tipo de estudo: Etiology_studies / Prevalence_studies / Risk_factors_studies Limite: Female / Humans / Pregnancy País/Região como assunto: Europa Idioma: En Revista: Birth Defects Res Ano de publicação: 2022 Tipo de documento: Article