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Epidemiology of congenital cerebral anomalies in Europe: a multicentre, population-based EUROCAT study.
Morris, Joan K; Wellesley, Diana G; Barisic, Ingeborg; Addor, Marie-Claude; Bergman, Jorieke E H; Braz, Paula; Cavero-Carbonell, Clara; Draper, Elizabeth S; Gatt, Miriam; Haeusler, Martin; Klungsoyr, Kari; Kurinczuk, Jennifer J; Lelong, Natalie; Luyt, Karen; Lynch, Catherine; O'Mahony, Mary T; Mokoroa, Olatz; Nelen, Vera; Neville, Amanda J; Pierini, Anna; Randrianaivo, Hanitra; Rankin, Judith; Rissmann, Anke; Rouget, Florence; Schaub, Bruno; Tucker, David F; Verellen-Dumoulin, Christine; Wiesel, Awi; Zymak-Zakutnia, Natalia; Lanzoni, Monica; Garne, Ester.
Afiliação
  • Morris JK; Population Health Research Institute, St George's, University of London, London, UK.
  • Wellesley DG; Department Clinical Genetics, University Hospital Southampton NHS Foundation Trust, Southampton, UK.
  • Barisic I; Children's Hospital Zagreb, Centre of Excellence for Reproductive and Regenerative Medicine, Medical School University of Zagreb, Zagreb, Croatia.
  • Addor MC; Department of Mother-Woman-Child, University Hospital Center, Lausanne, Switzerland.
  • Bergman JEH; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
  • Braz P; Department of Epidemiology, National Institute of Health Doutor Ricardo Jorge, Lisbon, Portugal.
  • Cavero-Carbonell C; Rare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region, Valencia, Spain.
  • Draper ES; Department of Health Sciences, University of Leicester, Leicester, UK.
  • Gatt M; Department of Health Information and Research, National Obstetric Information Systems, Valletta, Malta.
  • Haeusler M; Department of Obstetrics, Medical University of Graz, Graz, Austria.
  • Klungsoyr K; Division of Mental and Physical Health, Norwegian Institute of Public Health, Bergen and Department of Global Public Health and Primary Care, University of Bergen, Bergen, Norway.
  • Kurinczuk JJ; National Perinatal Epidemiology Unit, University of Oxford, Oxford, UK.
  • Lelong N; Paris Registry of Congenital Malformations, Obstetrical, Perinatal and Pediatric Epidemiology Research Team, Center for Biostatistics and Epidemiology, INSERM, Paris, France.
  • Luyt K; Translational Health Sciences, University of Bristol Medical School, Bristol, Bristol, UK.
  • Lynch C; Department of Public Health, Health Service Executive-South, Kilkenny, Ireland.
  • O'Mahony MT; Department of Public Health, Health Service Executive-South, Cork, Ireland.
  • Mokoroa O; Public Health Department of Gipuzkoa, Biodonostia Instituto de Investigacion Sanitaria, Donostia-San Sebastian, Spain.
  • Nelen V; Provinciaal Instituut voor Hygiene, Antwerpen, Belgium.
  • Neville AJ; IMER Registry, University of Ferrara and St Anna University Hospital, Ferrara, Italy.
  • Pierini A; Tuscany Registry of Congenital Defects, National Research Council Institute of Clinical Physiology/Fondazione Toscana Gabriele Monasterio, Pisa, Italy.
  • Randrianaivo H; Registre des Malformations Congenitales de la Reunion, Saint Pierre, Réunion, France.
  • Rankin J; Institute of Health & Society, Newcastle University, Newcastle, UK.
  • Rissmann A; Malformation Monitoring Centre Saxony-Anhalt, Medical Faculty Otto-von-Guericke University, Magdeburg, Germany.
  • Rouget F; Brittany Registry of Congenital Anomalies, Univ Rennes, CHU Rennes,Inserm, EHESP, Rennes, France.
  • Schaub B; Maison de la Femme de la Mère et de l'Enfant, University Hospital of Martinique, Fort-de-France, Martinique.
  • Tucker DF; Congenital Anomaly Register and Information Service for Wales, Public Health Wales, Swansea, UK.
  • Verellen-Dumoulin C; Center for Human Genetics, Institut de Pathologie et de Génétique, Charleroi, Belgium.
  • Wiesel A; Mainz Model Birth Registry, Center of Child and Adolescence Medicine, University Medical Center, Mainz, Germany.
  • Zymak-Zakutnia N; OMNI-Net Ukraine, Khmelnytsky City Children's Hospital, Khmelnytsky, Ukraine.
  • Lanzoni M; European Commission, Joint Research Centre (JRC), Ispra, Italy.
  • Garne E; Paediatric Department, Hospital Lillebaelt, Kolding, Denmark.
Arch Dis Child ; 104(12): 1181-1187, 2019 12.
Article em En | MEDLINE | ID: mdl-31243007
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anormalidades Congênitas / Sistema de Registros / Vigilância da População Tipo de estudo: Clinical_trials / Prevalence_studies / Risk_factors_studies / Screening_studies Limite: Child / Child, preschool / Female / Humans / Infant / Newborn / Pregnancy País/Região como assunto: Europa Idioma: En Revista: Arch Dis Child Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Reino Unido País de publicação: Reino Unido
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anormalidades Congênitas / Sistema de Registros / Vigilância da População Tipo de estudo: Clinical_trials / Prevalence_studies / Risk_factors_studies / Screening_studies Limite: Child / Child, preschool / Female / Humans / Infant / Newborn / Pregnancy País/Região como assunto: Europa Idioma: En Revista: Arch Dis Child Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Reino Unido País de publicação: Reino Unido