EUROlinkCAT protocol for a European population-based data linkage study investigating the survival, morbidity and education of children with congenital anomalies

Autor: Nathalie Lelong, Babak Khoshnood, David Tucker, Mika Gissler, Maria Loane, Ingeborg Barisic, Miriam Gatt, Kari Klungsoyr, Amanda Neville, Anna Pierini, Anke Rissmann, Oscar Zurriaga, Joan K Morris, Paula Braz, Vera Nelen, Judith Rankin, Ester Garne, Sue Jordan, Anna Heino, Silvia Baldacci, Michele Santoro, Alessio Coi, Lorena Mezzasalma, Daniel Thayer, Svetlana V Glinianaia, Hermien de Walle, Guy Thys, Anna Latos-Bielenska, Aurora Puccini, Elisa Ballardini, Wladimir Wertelecki, Carlos Matias Dias, Gianni Astolfi, James Densem, Joachim Tan, Joanne Emma Given, Hugh Claridge, Abigail Reid, Liz Limb, Gillian Briggs, Nicholas Connor, Stine Kjaer Urhoj, Mads Damkjær, Christina Neergaard Pedersen, Annarita Armaroli, Ljubica Boban, L Renée Lutke, Nicole H A Siemensma-Mühlenberg, Nathalie Bertille, Makan Rahshenas, Clara Cavero Carbonell, Laia Barrachina Bonet, Laura García Villodre, Anna Jamry-Dziurla, Sonja Kiuru-Kuhlefelt, Lyubov Yevtushok, Nataliia Zymak-Zakutnia, Diana Akhmedzhanova, Lyubov Ostapchuk, Oksana Tsizh, Serhii Lapchenko, Ausenda Machado, Ana João Santos, Liliana Antunes, Hanitra Randrianaivo-Ranjatoelina, Elly Den Hond, Olatz Mokoroa Carollo, Ieuan Scanlon

Publikováno v: BMJ Open, Vol 11, Iss 6 (2021)

Introduction Congenital anomalies (CAs) are a major cause of infant mortality, childhood morbidity and long-term disability. Over 130 000 children born in Europe every year will have a CA. This paper describes the EUROlinkCAT study, which is investig

Externí odkaz: https://doaj.org/article/71d0d10a7c8340b8864daf7f71f7e0a9

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

Autor: Judith Rankin, David Tucker, Olatz Mokoroa, Miriam Gatt, Anke Rissmann, Mary O'Mahony, Catherine Lynch, Amanda J. Neville, Marie-Claude Addor, Monica Lanzoni, Ester Garne, Hanitra Randrianaivo-Ranjatoelina, Ingeborg Barišić, Joan K. Morris, Vera Nelen, Natalya Zymak-Zakutnia, Fabrizio Bianchi, Maria Loane, H. E. K. De Walle

Publikováno v: Morris, J K, Garne, E, Loane, M, Addor, M C, Barisic, I, Bianchi, F, Gatt, M, Lanzoni, M, Lynch, C, Mokoroa, O, Nelen, V, Neville, A, O'Mahony, M T, Randrianaivo-Ranjatoelina, H, Rissmann, A, Tucker, D, de Walle, H E K, Zymak-Zakutnia, N & Rankin, J 2018, ' Prevalence of valproate syndrome in Europe from 2005 to 2014 : A registry based multi-centre study ', European Journal of Medical Genetics, vol. 61, no. 9, pp. 479-482 . https://doi.org/10.1016/j.ejmg.2018.05.008
European journal of medical genetics, 61(9), 479-482. ELSEVIER SCIENCE BV

Women with epilepsy need to continue to take anticonvulsants during their pregnancies to prevent seizures from occurring. Since the 1980's, it has been known that the use of valproate (an anticonvulsant) in the first trimester of pregnancy is associa

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00a2b548fda0fb6919f17c5f1e945e5d
https://pubmed.ncbi.nlm.nih.gov/29753923

Paper 6: EUROCAT member registries: organization and activities

Autor: Anna Latos-Bielenska, Patricia A. Boyd, Christine Verellen-Dumoulin, Carmel Mullaney, Karin Källén, Bérénice Doray, Marian K. Bakker, Vera Nelen, Babak Khoshnood, Antonin Sipek, Stein Emil Vollset, Annukka Ritvanen, Bob McDonnell, Ester Garne, Hanitra Randrianaivo-Ranjatoelina, Anna Materna-Kiryluk, Annette Queisser-Luft, Joaquin Salvador, Amanda J. Neville, Emmanuelle Amar, Anke Rissmann, David Tucker, Martin Haeusler, Miriam Gatt, Elizabeth S Draper, Elisa Calzolari, Ruth Greenlees, Anna Pierini, Mary O'Mahony, Larraitz Arriola, Wladimir Wertelecki, Judith Rankin, Marie-Claude Addor, Diana Wellesley, Carlos Matias Dias, Ingeborg Barišić, María Luisa Martínez-Frías

Publikováno v: Greenlees, R, Neville, A, Addor, M-C, Amar, E, Arriola, L, Bakker, M, Barisic, I, Boyd, P A, Calzolari, E, Doray, B, Draper, E, Vollset, S E, Garne, E, Gatt, M, Haeusler, M, Kallen, K, Khoshnood, B, Latos-Bielenska, A, Martinez-Frias, M-L, Materna-Kiryluk, A, Dias, C M, McDonnell, B, Mullaney, C, Nelen, V, O'Mahony, M, Pierini, A, Queisser-Luft, A, Randrianaivo-Ranjatoélina, H, Rankin, J, Rissmann, A, Ritvanen, A, Salvador, J, Sipek, A, Tucker, D, Verellen-Dumoulin, C, Wellesley, D & Wertelecki, W 2011, ' Paper 6: EUROCAT member registries: organization and activities ', Birth Defects Research. Part A: Clinical and Molecular Teratology, vol. 91 Suppl 1, pp. S51-S100 . https://doi.org/10.1002/bdra.20775
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname

BACKGROUND: EUROCAT is a network of population-based congenital anomaly registries providing standardized epidemiologic information on congenital anomalies in Europe. There are three types of EUROCAT membership: full, associate, or affiliate. Full me

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7d1c7f492f31bb9ed73998644a015a8
https://pubmed.ncbi.nlm.nih.gov/21381185