Catherine Rounding
AuthID: R-00F-JFX
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TITLE: Estimating Global Burden of Disease due to congenital anomaly: an analysis of European data
AUTHORS: Breidge Boyle; Marie Claude Addor; Larraitz Arriola; Ingeborg Barisic; Fabrizio Bianchi; Melinda Csaky Szunyogh; Hermien E K de Walle; Carlos Matias Dias; Elizabeth Draper; Miriam Gatt; Ester Garne; Martin Haeusler; Karin Kallen; Anna Latos Bielenska; Bob McDonnell; Carmel Mullaney; Vera Nelen; Amanda J Neville; Mary O'Mahony; Annette Queisser Wahrendorf; ...More
PUBLISHED: 2018, SOURCE: ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, VOLUME: 103, ISSUE: 1
AUTHORS: Breidge Boyle; Marie Claude Addor; Larraitz Arriola; Ingeborg Barisic; Fabrizio Bianchi; Melinda Csaky Szunyogh; Hermien E K de Walle; Carlos Matias Dias; Elizabeth Draper; Miriam Gatt; Ester Garne; Martin Haeusler; Karin Kallen; Anna Latos Bielenska; Bob McDonnell; Carmel Mullaney; Vera Nelen; Amanda J Neville; Mary O'Mahony; Annette Queisser Wahrendorf; ...More
PUBLISHED: 2018, SOURCE: ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, VOLUME: 103, ISSUE: 1
INDEXED IN: WOS
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TITLE: Epidemiology of congenital diaphragmatic hernia in Europe: a register-based study
AUTHORS: Mark R McGivern; Kate E Best; Judith Rankin; Diana Wellesley; Ruth Greenlees; Marie Claude Addor; Larraitz Arriola; Hermien de Walle; Ingeborg Barisic; Judit Beres; Fabrizio Bianchi; Elisa Calzolari; Berenice Doray; Elizabeth S Draper; Ester Garne; Miriam Gatt; Martin Haeusler; Babak Khoshnood; Kari Klungsoyr; Anna Latos Bielenska; ...More
PUBLISHED: 2015, SOURCE: ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, VOLUME: 100, ISSUE: 2
AUTHORS: Mark R McGivern; Kate E Best; Judith Rankin; Diana Wellesley; Ruth Greenlees; Marie Claude Addor; Larraitz Arriola; Hermien de Walle; Ingeborg Barisic; Judit Beres; Fabrizio Bianchi; Elisa Calzolari; Berenice Doray; Elizabeth S Draper; Ester Garne; Miriam Gatt; Martin Haeusler; Babak Khoshnood; Kari Klungsoyr; Anna Latos Bielenska; ...More
PUBLISHED: 2015, SOURCE: ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, VOLUME: 100, ISSUE: 2
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TITLE: Congenital Anomalies Associated with Trisomy 18 or Trisomy 13: A Registry-Based Study in 16 European Countries, 2000-2011. Anomalies associated with trisomies 18 or 13 Full Text
AUTHORS: Anna Springett; Diana Wellesley; Ruth Greenlees; Maria Loane; Marie Claude Addor; Larraitz Arriola; Jorieke Bergman; Clara Cavero Carbonell; Melinda Csaky Szunyogh; Elizabeth S Draper; Ester Garne; Miriam Gatt; Martin Haeusler; Babak Khoshnood; Kari Klungsoyr; Catherine Lynch; Carlos Matias Dias; Robert McDonnell; Vera Nelen; Mary O'Mahony; ...More
PUBLISHED: 2015, SOURCE: AMERICAN JOURNAL OF MEDICAL GENETICS PART A, VOLUME: 167, ISSUE: 12
AUTHORS: Anna Springett; Diana Wellesley; Ruth Greenlees; Maria Loane; Marie Claude Addor; Larraitz Arriola; Jorieke Bergman; Clara Cavero Carbonell; Melinda Csaky Szunyogh; Elizabeth S Draper; Ester Garne; Miriam Gatt; Martin Haeusler; Babak Khoshnood; Kari Klungsoyr; Catherine Lynch; Carlos Matias Dias; Robert McDonnell; Vera Nelen; Mary O'Mahony; ...More
PUBLISHED: 2015, SOURCE: AMERICAN JOURNAL OF MEDICAL GENETICS PART A, VOLUME: 167, ISSUE: 12
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TITLE: Hirschsprung's Disease Prevalence in Europe: A Register Based Study. Hirschsprung's Disease in Europe Full Text
AUTHORS: 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; ...More
PUBLISHED: 2014, SOURCE: BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY, VOLUME: 100, ISSUE: 9
AUTHORS: 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; ...More
PUBLISHED: 2014, SOURCE: BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY, VOLUME: 100, ISSUE: 9
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TITLE: Major Congenital Anomalies in Babies Born With Down Syndrome: A EUROCAT Population-Based Registry Study Full Text
AUTHORS: Joan K Morris; Ester Garne; Diana Wellesley; Marie Claude Addor; Larraitz Arriola; Ingeborg Barisic; Judit Beres; Fabrizio Bianchi; Judith Budd; Carlos Matias Dias; Miriam Gatt; Kari Klungsoyr; Babak Khoshnood; Anna Latos Bielenska; Carmel Mullaney; Vera Nelen; Amanda J Neville; Mary O'Mahony; Annette Queisser Luft; Hanitra Randrianaivo; ...More
PUBLISHED: 2014, SOURCE: AMERICAN JOURNAL OF MEDICAL GENETICS PART A, VOLUME: 164A, ISSUE: 12
AUTHORS: Joan K Morris; Ester Garne; Diana Wellesley; Marie Claude Addor; Larraitz Arriola; Ingeborg Barisic; Judit Beres; Fabrizio Bianchi; Judith Budd; Carlos Matias Dias; Miriam Gatt; Kari Klungsoyr; Babak Khoshnood; Anna Latos Bielenska; Carmel Mullaney; Vera Nelen; Amanda J Neville; Mary O'Mahony; Annette Queisser Luft; Hanitra Randrianaivo; ...More
PUBLISHED: 2014, SOURCE: AMERICAN JOURNAL OF MEDICAL GENETICS PART A, VOLUME: 164A, ISSUE: 12
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TITLE: Holt Oram syndrome: a registry-based study in Europe Full Text
AUTHORS: Ingeborg Barisic; Ljubica Boban; Ruth Greenlees; Ester Garne; Diana Wellesley; Elisa Calzolari; Marie Claude Addor; Larraitz Arriola; Jorieke E H Bergman; Paula Braz; Judith L S Budd; Miriam Gatt; Martin Haeusler; Babak Khoshnood; Kari Klungsoyr; Bob McDonnell; Vera Nelen; Anna Pierini; Annette Queisser Wahrendorf; Judith Rankin; ...More
PUBLISHED: 2014, SOURCE: ORPHANET JOURNAL OF RARE DISEASES, VOLUME: 9, ISSUE: 1
AUTHORS: Ingeborg Barisic; Ljubica Boban; Ruth Greenlees; Ester Garne; Diana Wellesley; Elisa Calzolari; Marie Claude Addor; Larraitz Arriola; Jorieke E H Bergman; Paula Braz; Judith L S Budd; Miriam Gatt; Martin Haeusler; Babak Khoshnood; Kari Klungsoyr; Bob McDonnell; Vera Nelen; Anna Pierini; Annette Queisser Wahrendorf; Judith Rankin; ...More
PUBLISHED: 2014, SOURCE: ORPHANET JOURNAL OF RARE DISEASES, VOLUME: 9, ISSUE: 1
INDEXED IN: WOS CrossRef