ProfileOfResearchers

Identificadas 6

1

TÃTULO: Estimating Global Burden of Disease due to congenital anomaly: an analysis of European data
AUTORES: 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; Hanitra Randrianaivo; Judith Rankin; Anke Rissmann; Annukka Ritvanen; Catherine Rounding; David Tucker; Christine Verellen Dumoulin; Diana Wellesley; Ben Wreyford; Natalia Zymak Zakutnia; Helen Dolk; ...Mais
PUBLICAÇÃO: 2018, FONTE: ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, VOLUME: 103, NÚMERO: 1

INDEXADO EM:

WOS

2

TÃTULO: Epidemiology of congenital diaphragmatic hernia in Europe: a register-based study
AUTORES: 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; Mary O'Mahony; Paula Braz; Bob McDonnell; Carmel Mullaney; Vera Nelen; Anette Queisser Luft; Hanitra Randrianaivo; Anke Rissmann; Catherine Rounding; Antonin Sipek; Rosie Thompson; David Tucker; Wladimir Wertelecki; Carmen Martos; ...Mais
PUBLICAÇÃO: 2015, FONTE: ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, VOLUME: 100, NÚMERO: 2

INDEXADO EM:

Scopus

WOS

3

TÃTULO: 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
AUTORES: 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; Anna Pierini; Annette Queisser Luft; Judith Rankin; Anke Rissmann; Catherine Rounding; Sylvia Stoianova; David Tuckerz; Natalya Zymak Zakutnia; Joan K Morris; ...Mais
PUBLICAÇÃO: 2015, FONTE: AMERICAN JOURNAL OF MEDICAL GENETICS PART A, VOLUME: 167, NÚMERO: 12

INDEXADO EM:

Scopus

WOS

4

TÃTULO: Hirschsprung's Disease Prevalence in Europe: A Register Based Study. Hirschsprung's Disease in Europe Full Text
AUTORES: 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; ...Mais
PUBLICAÇÃO: 2014, FONTE: BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY, VOLUME: 100, NÚMERO: 9

INDEXADO EM:

Scopus

WOS

5

TÃTULO: Major Congenital Anomalies in Babies Born With Down Syndrome: A EUROCAT Population-Based Registry Study Full Text
AUTORES: 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; Judith Rankin; Anke Rissmann; Cath Rounding; Antonin Sipek; Sylvia Stoianova; David Tucker; Hermien de Walle; Lyubov Yevtushok; Maria Loane; Helen Dolk; ...Mais
PUBLICAÇÃO: 2014, FONTE: AMERICAN JOURNAL OF MEDICAL GENETICS PART A, VOLUME: 164A, NÚMERO: 12

INDEXADO EM:

Scopus

WOS

6

TÃTULO: Holt Oram syndrome: a registry-based study in Europe Full Text
AUTORES: 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; Anke Rissmann; Catherine Rounding; David Tucker; Christine Verellen Dumoulin; Helen Dolk; ...Mais
PUBLICAÇÃO: 2014, FONTE: ORPHANET JOURNAL OF RARE DISEASES, VOLUME: 9, NÚMERO: 1

INDEXADO EM:

WOS

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