Methadone, Pierre Robin sequence and other congenital anomalies

Autor: Anke Rissmann, Brian Cleary, Hermien E. K. de Walle, Kari Klungsøyr, Anna Pierini, Oscar Zurriaga, Maria Loane, Amanda J. Neville, Marie-Claude Addor, Helen Dolk, Carlos Matias Dias, David Tucker, Miriam Gatt, Bob McDonnell, Ingeborg Barišić

Publikováno v: Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, 105(2), F151-F157. BMJ PUBLISHING GROUP

ObjectiveMethadone is a vital treatment for women with opioid use disorder in pregnancy. Previous reports suggested an association between methadone exposure and Pierre Robin sequence (PRS), a rare craniofacial anomaly. We assessed the association be

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5cf0c7f3aa8088e7de2b07b54fe52da
https://doi.org/10.1136/archdischild-2019-316804

Estimating Global Burden of Disease due to congenital anomaly: an analysis of European data

Autor: Vera Nelen, Hermien E. K. de Walle, Anke Rissmann, Ben Wreyford, Larraitz Arriola, Anna Latos-Bielenska, Carmel Mullaney, Christine Verellen-Dumoulin, Mary O'Mahony, Annukka Ritvanen, Breidge Boyle, Annette Queisser-Wahrendorf, Martin Haeusler, Natalia Zymak-Zakutnia, Elizabeth S Draper, Judith Rankin, Amanda J. Neville, Karin Källén, Marie-Claude Addor, Helen Dolk, David Tucker, Miriam Gatt, Hanitra Randrianaivo, Carlos Matias Dias, Diana Wellesley, Catherine Rounding, Bob McDonnell, Ester Garne, Ingeborg Barišić, Melinda Csáky-Szunyogh, Fabrizio Bianchi

Publikováno v: ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, 103(1), F22-F28. BMJ PUBLISHING GROUP
Archives of Disease in Childhood. Fetal and Neonatal Edition
Boyle, B, Addor, M-C, Arriola, L, Barisic, I, Bianchi, F, Csáky-Szunyogh, M, de Walle, H E K, Dias, C M, Draper, E, Gatt, M, Garne, E, Haeusler, M, Källén, K, Latos-Bielenska, A, McDonnell, B, Mullaney, C, Nelen, V, Neville, A J, O'Mahony, M, Queisser-Wahrendorf, A, Randrianaivo, H, Rankin, J, Rissmann, A, Ritvanen, A, Rounding, C, Tucker, D, Verellen-Dumoulin, C, Wellesley, D, Wreyford, B, Zymak-Zakutnia, N & Dolk, H 2018, ' Estimating Global Burden of Disease due to congenital anomaly : an analysis of European data ', Archives of Disease in Childhood, vol. 103, no. 1, pp. F22-F28 . https://doi.org/10.1136/archdischild-2016-311845
Boyle, B, Addor, M-C, Arriola, L, Barisic, I, Bianchi, F, Csáky-Szunyogh, M, de Walle, H E K, Dias, C M, Draper, E, Gatt, M, Garne, E, Haeusler, M, Källén, K, Latos-Bielenska, A, McDonnell, B, Mullaney, C, Nelen, V, Neville, A J, O'Mahony, M, Queisser-Wahrendorf, A, Randrianaivo, H, Rankin, J, Rissmann, A, Ritvanen, A, Rounding, C, Tucker, D, Verellen-Dumoulin, C, Wellesley, D, Wreyford, B, Zymak-Zakutnia, N & Dolk, H 2017, ' Estimating Global Burden of Disease due to congenital anomaly: an analysis of European data ', Archives of Disease in Childhood-Fetal and Neonatal Edition, vol. 103, pp. f22 . https://doi.org/10.1136/archdischild-2016-311845
Archives of disease in childhood. Fetal and neonatal edition, vol. 103, no. 1, pp. F22-F28

ObjectiveTo validate the estimates of Global Burden of Disease (GBD) due to congenital anomaly for Europe by comparing infant mortality data collected by EUROCAT registries with the WHO Mortality Database, and by assessing the significance of stillbi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2193f14916de688b1ec6535fa52e0785
https://www.bib.irb.hr/1170355

Epidemiology of congenital diaphragmatic hernia in Europe: a register-based study

Autor: Marie-Claude Addor, Diana Wellesley, Judith Rankin, Ingeborg Barišić, L. Arriola, Anke Rissmann, Hanitra Randrianaivo, Vera Nelen, Catherine Rounding, Paula Braz, Bob McDonnell, Ester Garne, Antonin Sipek, Martin Haeusler, Anette Queisser-Luft, Bérénice Doray, Elizabeth S Draper, Wladimir Wertelecki, Kari Klungsøyr, Kate E. Best, Anna Latos-Bielenska, Elisa Calzolari, Fabrizio Bianchi, Mary O'Mahony, Carmel Mullaney, Rosie Thompson, Judit Béres, Ruth Greenlees, Hermien E. K. de Walle, Mark R. McGivern, Babak Khoshnood, David Tucker, Miriam Gatt, Carmen Martos

Publikováno v: ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, 100(2), F137-F144. BMJ PUBLISHING GROUP
ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION
r-FISABIO. Repositorio Institucional de Producción Científica
instname
r-FISABIO: Repositorio Institucional de Producción Científica
Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (FISABIO)
McGivern, M R, Best, K E, Rankin, J, Wellesley, D, Greenlees, R, Addor, M-C, Arriola, L, de Walle, H, Barisic, I, Beres, J, Bianchi, F, Calzolari, E, Doray, B, Draper, E S, Garne, E, Gatt, M, Haeusler, M, Khoshnood, B, Klungsoyr, K, Latos-Bielenska, A, O'Mahony, M, Braz, P, McDonnell, B, Mullaney, C, Nelen, V, Queisser-Luft, A, Randrianaivo, H, Rissmann, A, Rounding, C, Sipek, A, Thompson, R, Tucker, D, Wertelecki, W & Martos, C 2015, ' Epidemiology of congenital diaphragmatic hernia in Europe : a register-based study ', Archives of Disease in Childhood. Fetal and Neonatal Edition, vol. 100, no. 2, pp. F137-F144 . https://doi.org/10.1136/archdischild-2014-306174

INTRODUCTION: Published prevalence rates of congenital diaphragmatic hernia (CDH) vary. This study aims to describe the epidemiology of CDH using data from high-quality, population-based registers belonging to the European Surveillance of Congenital

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4db2377eca8b940304dc2a577bde8b69
https://pubmed.ncbi.nlm.nih.gov/25411443

Hirschsprung's Disease Prevalence in Europe: A Register Based Study

Autor: Kate E, Best, Marie-Claude, Addor, Larraitz, Arriola, Eszter, Balku, Ingeborg, Barisic, Fabrizio, Bianchi, Elisa, Calzolari, Rhonda, Curran, Berenice, Doray, Elizabeth, Draper, Ester, Garne, Miriam, Gatt, Martin, Haeusler, Jorieke, Bergman, Babak, Khoshnood, Kari, Klungsoyr, Carmen, Martos, Anna, Materna-Kiryluk, Carlos, Matias Dias, Bob, McDonnell, Carmel, Mullaney, Vera, Nelen, Mary, O'Mahony, Annette, Queisser-Luft, Hanitra, Randrianaivo, Anke, Rissmann, Catherine, Rounding, Antonin, Sipek, Rosie, Thompson, David, Tucker, Diana, Wellesley, Natalya, Zymak-Zakutnia, Judith, Rankin

Publikováno v: Birth Defects Research. Part A: Clinical and Molecular Teratology, 100(9), 695-702. Wiley-Blackwell
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY
r-FISABIO. Repositorio Institucional de Producción Científica
instname
Best, K E, Addor, M-C, Arriola, L, Balku, E, Barisic, I, Bianchi, F, Calzolari, E, Curran, R, Doray, B, Draper, E, Garne, E, Gatt, M, Haeusler, M, Bergman, J, Khoshnood, B, Klungsoyr, K, Martos, C, Materna-Kiryluk, A, Matias Dias, C, McDonnell, B, Mullaney, C, Nelen, V, O'Mahony, M, Queisser-Luft, A, Randrianaivo, H, Rissmann, A, Rounding, C, Sipek, A, Thompson, R, Tucker, D, Wellesley, D, Zymak-Zakutnia, N & Rankin, J 2014, ' Hirschsprung's disease prevalence in Europe. A register based study ', Birth Defects Research. Part A: Clinical and Molecular Teratology, vol. 100, no. 9, pp. 695-702 . https://doi.org/10.1002/bdra.23269

Background: Hirschsprung's disease is a congenital gut motility disorder, characterised by the absence of the enteric ganglion cells along the distal gut. The aim of this study was to describe the epidemiology of Hirschsprung's disease, including add

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::03186882704b91eecd9a2db5c8f6f605
https://research.rug.nl/en/publications/71d00052-685d-4fe7-bd7b-0d4a60cc9a9d

Epidemiology of multiple congenital anomalies in Europe : A EUROCAT population-based registry study

Autor: Kari Klungsøyr, Joan K. Morris, Amanda J. Neville, Helen Dolk, Hermien E. K. de Walle, Judith Rankin, Elisa Calzolari, Anke Rissmann, Babak Khoshnood, Larraitz Arriola, Fabrizio Bianchi, Annette Queisser-Luft, Ingeborg Barišić, Maria Loane, Marie-Claude Addor, Diana Wellesley, Judith L. S. Budd, Vera Nelen, Christine Verellen-Dumoulin, Catherine Rounding, Bob McDonnell, Ester Garne, David Tucker

Publikováno v: Birth Defects Research. Part A: Clinical and Molecular Teratology, 100(4), 270-276. Wiley-Blackwell
Calzolari, E, Barisic, I, Loane, M, Morris, J, Wellesley, D, Dolk, H, Addor, M-C, Arriola, L, Bianchi, F, Neville, A J, Budd, J L S, Klungsoyr, K, Khoshnood, B, McDonnell, B, Nelen, V, Queisser-Luft, A, Rankin, J, Rissmann, A, Rounding, C, Tucker, D, Verellen-Dumoulin, C, de Walle, H & Garne, E 2014, ' Epidemiology of multiple congenital anomalies in Europe: A EUROCAT population-based registry study ', Birth Defects Research. Part A: Clinical and Molecular Teratology, vol. 100, no. 4, pp. 270-276 . https://doi.org/10.1002/bdra.23240

BACKGROUND: This study describes the prevalence, associated anomalies, and demographic characteristics of cases of multiple congenital anomalies (MCA) in 19 population-based European registries (EUROCAT) covering 959,446 births in 2004 and 2010.METHO

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a07e5576cf1586114ce3dc5b66c52c4
https://doi.org/10.1002/bdra.23240