Surveillance of multiple congenital anomalies; searching for new associations.

Autor: Morris JK; Population Health Research Institute, St George's, University of London, London, UK. jmorris@sgul.ac.uk., Bergman JEH; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands., Barisic I; Children's Hospital Zagreb, Centre of Excellence for Reproductive and Regenerative Medicine, Medical School University of Zagreb, Zagreb, Croatia., Wellesley D; Clinical Genetics, University of Southampton and Wessex Clinical Genetics Service, Princess Anne Hospital, Southampton, UK., Tucker D; Congenital Anomaly Register & Information Service for Wales (CARIS) Public Health Knowledge and Research, Public Health Wales, Swansea, Wales, UK., Limb E; Population Health Research Institute, St George's, University of London, London, UK., Addor MC; Department of Woman-Mother-Child, University Medical Center CHUV, Lausanne, Switzerland., Cavero-Carbonell C; Rare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region, Valencia, Spain., Matias Dias C; Epidemiology Department, National Institute of Health Doutor Ricardo Jorge, Lisboa, Portugal., Draper ES; Department of Population Health Sciences, Georg Davies Centre, University of Leicester, Leicester, UK., Echevarría-González-de-Garibay LJ; Department of Health of the Basque Government, Vitoria-Gasteiz, Spain., Gatt M; Malta Congenital Anomalies Registry, Directorate for Health Information and Research, Guardamangia, Malta., Klungsøyr K; Department of Global Public Health and Primary Care, University of Bergen, Bergen, Norway.; Division of Mental and Physical Health, Norwegian Institute of Public Health, Bergen, Norway., Lelong N; Université Paris Cité, CRESS, Équipe de recherche en épidémiologie obstétricale périnatale et pédiatrique (EPOPé), INSERM, INRA, Paris, France., Luyt K; South West Congenital Anomaly Register, Bristol Medical School, University of Bristol, Bristol, UK., Materna-Kiryluk A; Polish Registry of Congenital Malformations, Chair and Department of Medical Genetics, University of Medical Sciences, 61-701, Poznan, Poland., Nelen V; Provincial Institute for Hygiene, Antwerp, Belgium., Neville A; Center for Clinical and Epidemiological Research, University of Ferrara, Ferrara, Italy., Perthus I; 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., Pierini A; Unit of Epidemiology of Rare diseases and Congenital anomalies, Institute of Clinical Physiology, National Research Council, Pisa, Italy., Randrianaivo-Ranjatoelina H; Service de Génétique Médicale et d'oncogénétique, Registre des Malformations Congénitales, Saint Pierre, La Réunion, France., Rankin J; Population Health Sciences Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK., Rissmann A; Malformation Monitoring Centre Saxony-Anhalt, Medical Faculty Otto-von-Guericke University-Magdeburg, Magdeburg, Germany., Rouget F; Brittany Registry of Congenital Anomalies, CHU Rennes, Univ Rennes, Inserm, EHESP, Irset (Institut de recherche en santé, environnement et travail) - UMR_S 1085, F-35000, Rennes, France., Sayers G; Health Intelligence, Research and Development Health Service Executive, Dublin, Ireland., Wertelecki W; OMNI-Net Ukraine Programs, Rivne, Ukraine., Kinsner-Ovaskainen A; European Commission, Joint Research Centre, Ispra, Italy., Garne E; Department of Paediatrics and Adolescent Medicine, Lillebaelt Hospital, University Hospital of Southern Denmark, Kolding, Denmark.

Publikováno v: European journal of human genetics : EJHG [Eur J Hum Genet] 2024 Apr; Vol. 32 (4), pp. 407-412. Date of Electronic Publication: 2023 Dec 05.

Prevalence of valproate syndrome in Europe from 2005 to 2014: A registry based multi-centre study.

Autor: Morris JK; Wolfson Institute of Preventive Medicine Queen Mary University of London, UK. Electronic address: j.k.morris@qmul.ac.uk., Garne E; Paediatric Department, Hospital Lillebaelt, Kolding, Denmark., Loane M; Ulster University, UK., Addor MC; Service de Médecine Génétique, CHUV, Lausanne, Switzerland., Barisic I; Chlidren's Hospital Zagreb, Croatia., Bianchi F; Institute of Clinical Physiology-National Research Council (IFC-CNR), Pisa, Italy., Gatt M; Malta Congenital Anomalies Registry, Directorate for Health Information and Research, Malta., Lanzoni M; European Commission, DG Joint Research Centre, Ispra, Italy., Lynch C; HSE SE, Kilkenny, Ireland., Mokoroa O; Public Health Division of Gipuzkoa, Biodonostia Research Institute, Donostia-San Sebastian, Spain., Nelen V; PIH, Province of Antwerp, Department of Environment, Antwerp, Belgium., Neville A; Center for Clinical and Epidemiological Research, University of Ferrara, Italy., O'Mahony MT; HSE South (Cork & Kerry), Ireland., Randrianaivo-Ranjatoelina H; Chu Sud Reunion, St Pierre, Reunion., Rissmann A; Malformation Monitoring Centre Saxony-Anhalt, Medical Faculty Otto-von-Guericke University, Magdeburg, Germany., Tucker D; Public Health Wales NHS Trust, UK., de Walle HEK; University of Groningen, the Netherlands., Zymak-Zakutnia N; OMNI-Net Ukraine Birth Defects Program and Khmelnytsky City Children's Hospital, Ukraine., Rankin J; Institute of Health & Society, Newcastle University, UK.

Publikováno v: European journal of medical genetics [Eur J Med Genet] 2018 Sep; Vol. 61 (9), pp. 479-482. Date of Electronic Publication: 2018 May 18.

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Joint Effect of Maternal Tobacco Smoking and Pregestational Diabetes on Preterm Births and Congenital Anomalies: A Population-Based Study in Northern Italy.

Autor: Borsari, Lucia¹, Malagoli, Carlotta¹, Werler, Martha M.^2,3, Rothman, Kenneth J.^2,3,4, Malavolti, Marcella¹, Rodolfi, Rossella⁵, De Girolamo, Gianfranco⁶, Nicolini, Fausto⁵, Vinceti, Marco^1,2,3

Publikováno v: Journal of Diabetes Research. 6/28/2018, p1-7. 7p.

Assessing the role of multiple pregnancies in the association between tetralogy of Fallot and assisted reproductive techniques: a path-analysis approach.

Autor: Karim Tararbit¹ karim.tararbit@inserm.fr, Lelong, Nathalie¹ nathalie.lelong@inserm.fr, Houyel, Lucile² l.houyel@ccml.fr, Bonnet, Damien³ damien.bonnet@nck.aphp.fr, Goffinet, François^1,4 francois.goffinet@cch.aphp.fr, Babak Khoshnood¹ babak.khoshnood@inserm.fr

Publikováno v: Orphanet Journal of Rare Diseases. 2014, Vol. 9 Issue 1, p1-22. 22p.