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Epidemiology of Dandy-Walker Malformation in Europe: A EUROCAT Population-Based Registry Study.
Santoro, Michele; Coi, Alessio; Barisic, Ingeborg; Garne, Ester; Addor, Marie-Claude; Bergman, Jorieke E H; Bianchi, Fabrizio; Boban, Ljubica; Braz, Paula; Cavero-Carbonell, Clara; Gatt, Miriam; Haeusler, Martin; Kinsner-Ovaskainen, Agnieszka; Klungsøyr, Kari; Kurinczuk, Jennifer J; Lelong, Nathalie; Luyt, Karen; Materna-Kiryluk, Anna; Mokoroa, Olatz; Mullaney, Carmel; Nelen, Vera; Neville, Amanda Julie; O'Mahony, Mary T; Perthus, Isabelle; Randrianaivo, Hanitra; Rankin, Judith; Rissmann, Anke; Rouget, Florence; Schaub, Bruno; Tucker, David; Wellesley, Diana; Yevtushok, Lyubov; Pierini, Anna.
Afiliação
  • Santoro M; Institute of Clinical Physiology, National Research Council, Pisa, Italy, michele.santoro@ifc.cnr.it.
  • Coi A; Institute of Clinical Physiology, National Research Council, Pisa, Italy.
  • Barisic I; Children's Hospital Zagreb, Centre of Excellence for Reproductive and Regenerative Medicine, Medical School University of Zagreb, Zagreb, Croatia.
  • Garne E; Department of Paediatric, Hospital Lillebaelt, Kolding, Denmark.
  • Addor MC; Department of Woman-Mother-Child, University Medical Center CHUV, Lausanne, Switzerland.
  • Bergman JEH; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
  • Bianchi F; Institute of Clinical Physiology, National Research Council, Pisa, Italy.
  • Boban L; Fondazione Toscana Gabriele Monasterio, Pisa, Italy.
  • Braz P; Children's Hospital Zagreb, Centre of Excellence for Reproductive and Regenerative Medicine, Medical School University of Zagreb, Zagreb, Croatia.
  • Cavero-Carbonell C; Department of Epidemiology, National Institute of Health Doutor Ricardo Jorge, Lisbon, Portugal.
  • Gatt M; Rare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region, Valencia, Spain.
  • Haeusler M; Malta Congenital Anomalies Registry, Directorate for Health Information and Research, Pieta, Malta.
  • Kinsner-Ovaskainen A; Medical University of Graz, Graz, Austria.
  • Klungsøyr K; European Commission, Joint Research Centre, Ispra, Italy.
  • Kurinczuk JJ; 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.
  • Luyt K; National Perinatal Epidemiology Unit, Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom.
  • Materna-Kiryluk A; Paris Registry of Congenital Malformations, Inserm UMR 1153, Obstetrical, Perinatal and Pediatric Epidemiology Research Team (Epopé), Center for Epidemiology and Statistics Sorbonne Paris Cité, DHU Risks in Pregnancy, Paris Descartes University, Paris, France.
  • Mokoroa O; South West Congenital Anomaly Register, Bristol Medical School, University of Bristol, Bristol, United Kingdom.
  • Mullaney C; Department of Medical Genetics, Poznan University of Medical Sciences, Poznan, Poland.
  • Nelen V; Public Health Division of Gipuzkoa, Biodonostia Research Institute, Donostia-San Sebastian, Spain.
  • Neville AJ; Department of Public Health, HSE South East, Kilkenny, Ireland.
  • O'Mahony MT; Provincial Institute of Hygiene, Antwerp, Belgium.
  • Perthus I; IMER Registry (Emilia Romagna Registry of Birth Defects), Center for Clinical and Epidemiological Research, University of Ferrara Azienda Ospedaliero- Universitaria di Ferrara, Ferrara, Italy.
  • Randrianaivo H; Department of Public Health, HSE South, Cork and Kerry, Ireland.
  • Rankin J; Department of Clinical Genetics, Auvergne Registry of Congenital Anomalies (CEMC-Auvergne), Centre de Référence des Maladies Rares, University Hospital of Clermont-Ferrand, Clermont-Ferrand, France.
  • Rissmann A; Register of Congenital Malformations Isle of Reunion Ilsland, CHU St Pierre, La Reunion, France.
  • Rouget F; Institute of Health and Society, Newcastle University/National Congenital Anomaly and Rare Disease Registration Service (NCARDRS), Public Health England, London, United Kingdom.
  • Schaub B; Malformation Monitoring Centre Saxony-Anhalt, Medical Faculty Otto-von-Guericke University Magdeburg, Magdeburg, Germany.
  • Tucker D; Brittany Registry of Congenital Malformations, CHU Rennes, Univ Rennes, Inserm, EHESP, Irset (Institut de recherche en santé, environnement et travail), UMR_S 1085, 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 Bay, France.
  • Yevtushok L; Congenital Anomaly Register and Information Service for Wales (CARIS), Public Health Wales, Swansea, United Kingdom.
  • Pierini A; Wessex Clinical Genetics Service, University Hospitals Southampton, Southampton, United Kingdom.
Neuroepidemiology ; 53(3-4): 169-179, 2019.
Article em En | MEDLINE | ID: mdl-31302658
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Dandy-Walker Tipo de estudo: Diagnostic_studies / Risk_factors_studies / Screening_studies Limite: Adult / Female / Humans / Male / Pregnancy País/Região como assunto: Europa Idioma: En Revista: Neuroepidemiology Ano de publicação: 2019 Tipo de documento: Article País de publicação: Suíça
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Dandy-Walker Tipo de estudo: Diagnostic_studies / Risk_factors_studies / Screening_studies Limite: Adult / Female / Humans / Male / Pregnancy País/Região como assunto: Europa Idioma: En Revista: Neuroepidemiology Ano de publicação: 2019 Tipo de documento: Article País de publicação: Suíça