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Journal Abstract Search

332 related items for PubMed ID: 31243007

  • 1. Epidemiology of congenital cerebral anomalies in Europe: a multicentre, population-based EUROCAT study.
    Morris JK, Wellesley DG, Barisic I, Addor MC, Bergman JEH, Braz P, Cavero-Carbonell C, Draper ES, Gatt M, Haeusler M, Klungsoyr K, Kurinczuk JJ, Lelong N, Luyt K, Lynch C, O'Mahony MT, Mokoroa O, Nelen V, Neville AJ, Pierini A, Randrianaivo H, Rankin J, Rissmann A, Rouget F, Schaub B, Tucker DF, Verellen-Dumoulin C, Wiesel A, Zymak-Zakutnia N, Lanzoni M, Garne E.
    Arch Dis Child; 2019 Dec; 104(12):1181-1187. PubMed ID: 31243007
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  • 5. Trends in the prevalence, risk and pregnancy outcome of multiple births with congenital anomaly: a registry-based study in 14 European countries 1984-2007.
    Boyle B, McConkey R, Garne E, Loane M, Addor MC, Bakker MK, Boyd PA, Gatt M, Greenlees R, Haeusler M, Klungsøyr K, Latos-Bielenska A, Lelong N, McDonnell R, Métneki J, Mullaney C, Nelen V, O'Mahony M, Pierini A, Rankin J, Rissmann A, Tucker D, Wellesley D, Dolk H.
    BJOG; 2013 May; 120(6):707-16. PubMed ID: 23384325
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  • 7. Epidemiology of Dandy-Walker Malformation in Europe: A EUROCAT Population-Based Registry Study.
    Santoro M, Coi A, Barišić I, Garne E, Addor MC, Bergman JEH, Bianchi F, Boban L, Braz P, Cavero-Carbonell C, Gatt M, Haeusler M, Kinsner-Ovaskainen A, Klungsøyr K, Kurinczuk JJ, Lelong N, Luyt K, Materna-Kiryluk A, Mokoroa O, Mullaney C, Nelen V, Neville AJ, O'Mahony MT, Perthus I, Randrianaivo H, Rankin J, Rissmann A, Rouget F, Schaub B, Tucker D, Wellesley D, Yevtushok L, Pierini A.
    Neuroepidemiology; 2019 May; 53(3-4):169-179. PubMed ID: 31302658
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  • 8. Population-based surveillance of congenital anomalies over 40 years (1981-2020): Results from the Paris Registry of Congenital Malformations (remaPAR).
    Monier I, Hachem S, Goffinet F, Martinez-Marin A, Khoshnood B, Lelong N.
    J Gynecol Obstet Hum Reprod; 2024 Jun; 53(6):102780. PubMed ID: 38552958
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  • 10. Congenital anomalies associated with trisomy 18 or trisomy 13: A registry-based study in 16 European countries, 2000-2011.
    Springett A, Wellesley D, Greenlees R, Loane M, Addor MC, Arriola L, Bergman J, Cavero-Carbonell C, Csaky-Szunyogh M, Draper ES, Garne E, Gatt M, Haeusler M, Khoshnood B, Klungsoyr K, Lynch C, Dias CM, McDonnell R, Nelen V, O'Mahony M, Pierini A, Queisser-Luft A, Rankin J, Rissmann A, Rounding C, Stoianova S, Tuckerz D, Zymak-Zakutnia N, Morris JK.
    Am J Med Genet A; 2015 Dec; 167A(12):3062-9. PubMed ID: 26347425
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  • 12. Paper 3: EUROCAT data quality indicators for population-based registries of congenital anomalies.
    Loane M, Dolk H, Garne E, Greenlees R, EUROCAT Working Group.
    Birth Defects Res A Clin Mol Teratol; 2011 Mar; 91 Suppl 1():S23-30. PubMed ID: 21384530
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  • 16. Paper 1: The EUROCAT network--organization and processes.
    Boyd PA, Haeusler M, Barisic I, Loane M, Garne E, Dolk H.
    Birth Defects Res A Clin Mol Teratol; 2011 Mar; 91 Suppl 1():S2-15. PubMed ID: 21384531
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