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Signal Detection in EUROmediCAT: Identification and Evaluation of Medication-Congenital Anomaly Associations and Use of VigiBase as a Complementary Source of Reference.
Cavadino, Alana; Sandberg, Lovisa; Öhman, Inger; Bergvall, Tomas; Star, Kristina; Dolk, Helen; Loane, Maria; Addor, Marie-Claude; Barisic, Ingeborg; Cavero-Carbonell, Clara; Garne, Ester; Gatt, Miriam; Khoshnood, Babak; Klungsøyr, Kari; Latos-Bielenska, Anna; Lelong, Nathalie; Lutke, Reneé; Materna-Kiryluk, Anna; Nelen, Vera; Nevill, Amanda; O'Mahony, Mary; Mokoroa, Olatz; Pierini, Anna; Randrianaivo, Hanitra; Rissmann, Anke; Tucker, David; Wiesel, Awi; Yevtushok, Lyubov; Morris, Joan K.
Afiliação
  • Cavadino A; School of Population Health, the University of Auckland, Auckland, New Zealand.
  • Sandberg L; Uppsala Monitoring Centre, Uppsala, Sweden.
  • Öhman I; Uppsala Monitoring Centre, Uppsala, Sweden.
  • Bergvall T; Uppsala Monitoring Centre, Uppsala, Sweden.
  • Star K; Uppsala Monitoring Centre, Uppsala, Sweden.
  • Dolk H; Department of Public Health and Caring Sciences, Uppsala University, Uppsala, Sweden.
  • Loane M; Institute of Nursing and Health Research, Ulster University, Newtownabbey, Northern Ireland, UK.
  • Addor MC; Institute of Nursing and Health Research, Ulster University, Newtownabbey, Northern Ireland, UK.
  • Barisic I; Department of Woman-Mother-Child, University Hospital Center CHUV, CH 1011, Lausanne, Switzerland.
  • Cavero-Carbonell C; Children's Hospital Zagreb, Centre of Excellence for Reproductive and Regenerative Medicine, Medical School University of Zagreb, Zagreb, Croatia.
  • Garne E; Rare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region, Valencia, Spain.
  • Gatt M; Paediatric Department, Hospital Lillebaelt, Kolding, Denmark.
  • Khoshnood B; Malta Congenital Anomalies Registry, Directorate for Health Information and Research, Tal-Pietà, Malta.
  • Klungsøyr K; Paris Registry of Congenital Malformations, Obstetrical, Perinatal and Paediatric Epidemiology Research Team, Centre for Biostatistics and Epidemiology, INSERM, UMR 1153, Paris, France.
  • Latos-Bielenska A; Department of Global Public Health and Primary Care, University of Bergen, Bergen, Norway.
  • Lelong N; Department of Medical Genetics, Poznan University of Medical Sciences, Poznan, Poland.
  • Lutke R; Paris Registry of Congenital Malformations, Obstetrical, Perinatal and Paediatric Epidemiology Research Team, Centre for Biostatistics and Epidemiology, INSERM, UMR 1153, Paris, France.
  • Materna-Kiryluk A; Department of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands.
  • Nelen V; Department of Medical Genetics, Poznan University of Medical Sciences, Poznan, Poland.
  • Nevill A; Department of Environment, PIH, Antwerp, Belgium.
  • O'Mahony M; IMER Registry (Emila Romagna Registry of Birth Defects), Center for Clinical and Epidemiological Research, University of Ferrara, Azienda Ospedaliero, Italy.
  • Mokoroa O; Department of Public Health, Health Service Executive-South, Cork, Ireland.
  • Pierini A; Basque Government, Department of Health, Public Health Division of Gipuzkoa, Donostia-San Sebastian, Spain.
  • Randrianaivo H; Tuscany Registry of Congenital Defects (RTDC), Institute of Clinical Physiology, National Research Council/Fondazione Toscana Gabriele Monasterio, Pisa, Italy.
  • Rissmann A; Unit of congenital malformations, REMACOR- Medical School University of La Réunion St Pierre, Sainte-Clotilde, France.
  • Tucker D; Malformation Monitoring Centre Saxony-Anhalt, Medical Faculty Otto-von-Guericke-University, Magdeburg, Germany.
  • Wiesel A; Congenital Anomaly Register and Information Service for Wales, Public Health Wales Knowledge Directorate, Level 3, West Wing Block, Singleton Hospital, Sketty Lane, Swansea, UK.
  • Yevtushok L; Department of Pediatrics, Birth Registry Mainz Model, University Medical Center of Mainz, Mainz, Germany.
  • Morris JK; OMNI-Net Ukraine Birth Defects Program and Rivne Regional Medical Diagnostic Center, Rivne, Ukraine.
Drug Saf ; 44(7): 765-785, 2021 07.
Article em En | MEDLINE | ID: mdl-33966183
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Teratogênicos / Cardiopatias Congênitas Tipo de estudo: Diagnostic_studies / Qualitative_research / Risk_factors_studies Limite: Female / Humans / Pregnancy Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Teratogênicos / Cardiopatias Congênitas Tipo de estudo: Diagnostic_studies / Qualitative_research / Risk_factors_studies Limite: Female / Humans / Pregnancy Idioma: En Ano de publicação: 2021 Tipo de documento: Article