Amanda J. Neville
AuthID: R-00G-SV2
1
TÃTULO: COVID-19 and children with congenital anomalies: a European survey of parents' experiences of healthcare services Full Text
AUTORES: Latos Bielenska, Anna; Marcus, Elena; Jamry Dziurla, Anna; Rankin, Judith; Barisic, Ingeborg; Cavero Carbonell, Clara; Den Hond, Elly; Garne, Ester; Genard, Lucas; Santos, Ana Joao; Lutke, L. Renee; Dias, Carlos Matias; Pedersen, Christina Neergaard; Neville, Amanda; Niemann, Annika; Odak, Ljubica; Paramo Rodriguez, Lucia; Pierini, Anna; Rissmann, Anke; Morris, Joan K.;
PUBLICAÇÃO: 2022, FONTE: BMJ OPEN, VOLUME: 12, NÚMERO: 7
AUTORES: Latos Bielenska, Anna; Marcus, Elena; Jamry Dziurla, Anna; Rankin, Judith; Barisic, Ingeborg; Cavero Carbonell, Clara; Den Hond, Elly; Garne, Ester; Genard, Lucas; Santos, Ana Joao; Lutke, L. Renee; Dias, Carlos Matias; Pedersen, Christina Neergaard; Neville, Amanda; Niemann, Annika; Odak, Ljubica; Paramo Rodriguez, Lucia; Pierini, Anna; Rissmann, Anke; Morris, Joan K.;
PUBLICAÇÃO: 2022, FONTE: BMJ OPEN, VOLUME: 12, NÚMERO: 7
INDEXADO EM:
WOS
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2
TÃTULO: Amniotic band syndrome and limb body wall complex in Europe 1980-2019 Full Text
AUTORES: Bergman, Jorieke E. H.; Barisic, Ingeborg; Addor, Marie Claude; Braz, Paula; Cavero Carbonell, Clara; Draper, Elizabeth S.; Echevarria Gonzalez de Garibay, Luis J.; Gatt, Miriam; Haeusler, Martin; Khoshnood, Babak; Klungsoyr, Kari; Kurinczuk, Jennifer J.; Latos Bielenska, Anna; Luyt, Karen; Martin, Danielle; Mullaney, Carmel; Nelen, Vera; Neville, Amanda J.; O'Mahony, Mary T.; Perthus, Isabelle; ...Mais
PUBLICAÇÃO: 2022, FONTE: AMERICAN JOURNAL OF MEDICAL GENETICS PART A
AUTORES: Bergman, Jorieke E. H.; Barisic, Ingeborg; Addor, Marie Claude; Braz, Paula; Cavero Carbonell, Clara; Draper, Elizabeth S.; Echevarria Gonzalez de Garibay, Luis J.; Gatt, Miriam; Haeusler, Martin; Khoshnood, Babak; Klungsoyr, Kari; Kurinczuk, Jennifer J.; Latos Bielenska, Anna; Luyt, Karen; Martin, Danielle; Mullaney, Carmel; Nelen, Vera; Neville, Amanda J.; O'Mahony, Mary T.; Perthus, Isabelle; ...Mais
PUBLICAÇÃO: 2022, FONTE: AMERICAN JOURNAL OF MEDICAL GENETICS PART A
INDEXADO EM:
Scopus
WOS
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3
TÃTULO: Spectrum of congenital anomalies among VACTERL cases: a EUROCAT population-based study
AUTORES: Romy Van de Putte; Iris A L M Van Rooij; Carlo L M Marcelis; Michel H Guo; Han G Brunner; Marie Claude Addor; Clara Cavero Carbonell; Carlos M Dias; Elizabeth S Draper; Larraitz Etxebarriarteun; Miriam Gatt; Martin Haeusler; Babak Khoshnood; Kari Klungsoyr; Jenny J Kurinczuk; Monica Lanzoni; Anna Latos Bielenska; Karen Luyt; Mary T O'Mahony; Nicola Miller; ...Mais
PUBLICAÇÃO: 2020, FONTE: PEDIATRIC RESEARCH, VOLUME: 87, NÚMERO: 3
AUTORES: Romy Van de Putte; Iris A L M Van Rooij; Carlo L M Marcelis; Michel H Guo; Han G Brunner; Marie Claude Addor; Clara Cavero Carbonell; Carlos M Dias; Elizabeth S Draper; Larraitz Etxebarriarteun; Miriam Gatt; Martin Haeusler; Babak Khoshnood; Kari Klungsoyr; Jenny J Kurinczuk; Monica Lanzoni; Anna Latos Bielenska; Karen Luyt; Mary T O'Mahony; Nicola Miller; ...Mais
PUBLICAÇÃO: 2020, FONTE: PEDIATRIC RESEARCH, VOLUME: 87, NÚMERO: 3
INDEXADO EM:
Scopus
WOS
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4
TÃTULO: Maternal risk factors for the VACTERL association: A EUROCAT case-control study
AUTORES: Romy van de Putte; Iris A L M Van Rooij; Cynthia P Haanappel; Carlo L M Marcelis; Han G Brunner; Marie Claude Addor; Clara Cavero Carbonell; Carlos M Dias; Elizabeth S Draper; Larraitz Etxebarriarteun; Miriam Gatt; Babak Khoshnood; Agnieszka Kinsner Ovaskainen; Kari Klungsoyr; Jenny J Kurinczuk; Anna Latos Bielenska; Karen Luyt; Mary T O'Mahony; Nicola Miller; Carmel Mullaney; ...Mais
PUBLICAÇÃO: 2020, FONTE: BIRTH DEFECTS RESEARCH, VOLUME: 112, NÚMERO: 9
AUTORES: Romy van de Putte; Iris A L M Van Rooij; Cynthia P Haanappel; Carlo L M Marcelis; Han G Brunner; Marie Claude Addor; Clara Cavero Carbonell; Carlos M Dias; Elizabeth S Draper; Larraitz Etxebarriarteun; Miriam Gatt; Babak Khoshnood; Agnieszka Kinsner Ovaskainen; Kari Klungsoyr; Jenny J Kurinczuk; Anna Latos Bielenska; Karen Luyt; Mary T O'Mahony; Nicola Miller; Carmel Mullaney; ...Mais
PUBLICAÇÃO: 2020, FONTE: BIRTH DEFECTS RESEARCH, VOLUME: 112, NÚMERO: 9
INDEXADO EM:
Scopus
WOS
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5
TÃTULO: Epidemiology of congenital cerebral anomalies in Europe: a multicentre, population-based EUROCAT study
AUTORES: Joan K Morris; Diana G Wellesley; Ingeborg Barisic; Marie Claude Addor; Jorieke E H Bergman; Paula Braz; Clara Cavero Carbonell; Elizabeth S Draper; Miriam Gatt; Martin Haeusler; Kari Klungsoyr; Jennifer J Kurinczuk; Natalie Lelong; Karen Luyt; Catherine Lynch; Mary T O'Mahony; Olatz Mokoroa; Vera Nelen; Amanda J Neville; Anna Pierini; ...Mais
PUBLICAÇÃO: 2019, FONTE: ARCHIVES OF DISEASE IN CHILDHOOD, VOLUME: 104, NÚMERO: 12
AUTORES: Joan K Morris; Diana G Wellesley; Ingeborg Barisic; Marie Claude Addor; Jorieke E H Bergman; Paula Braz; Clara Cavero Carbonell; Elizabeth S Draper; Miriam Gatt; Martin Haeusler; Kari Klungsoyr; Jennifer J Kurinczuk; Natalie Lelong; Karen Luyt; Catherine Lynch; Mary T O'Mahony; Olatz Mokoroa; Vera Nelen; Amanda J Neville; Anna Pierini; ...Mais
PUBLICAÇÃO: 2019, FONTE: ARCHIVES OF DISEASE IN CHILDHOOD, VOLUME: 104, NÚMERO: 12
INDEXADO EM:
Scopus
WOS
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TÃTULO: Epidemiology of achondroplasia: A population-based study in Europe Full Text
AUTORES: Alessio Coi; Michele Santoro; Ester Garne; Anna Pierini; Marie Claude Addor; Jean Luc Alessandri; Jorieke E H Bergman; Fabrizio Bianchi; Ljubica Boban; Paula Braz; Clara Cavero Carbonell; Miriam Gatt; Martin Haeusler; Kari Klungsoyr; Jennifer J Kurinczuk; Monica Lanzoni; Nathalie Lelong; Karen Luyt; Olatz Mokoroa; Carmel Mullaney; ...Mais
PUBLICAÇÃO: 2019, FONTE: AMERICAN JOURNAL OF MEDICAL GENETICS PART A, VOLUME: 179, NÚMERO: 9
AUTORES: Alessio Coi; Michele Santoro; Ester Garne; Anna Pierini; Marie Claude Addor; Jean Luc Alessandri; Jorieke E H Bergman; Fabrizio Bianchi; Ljubica Boban; Paula Braz; Clara Cavero Carbonell; Miriam Gatt; Martin Haeusler; Kari Klungsoyr; Jennifer J Kurinczuk; Monica Lanzoni; Nathalie Lelong; Karen Luyt; Olatz Mokoroa; Carmel Mullaney; ...Mais
PUBLICAÇÃO: 2019, FONTE: AMERICAN JOURNAL OF MEDICAL GENETICS PART A, VOLUME: 179, NÚMERO: 9
INDEXADO EM:
Scopus
WOS
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7
TÃTULO: Epidemiology of Dandy-Walker Malformation in Europe: A EUROCAT Population-Based Registry Study
AUTORES: Michele Santoro; Alessio Coi; Ingeborg Barisic; Ester Garne; Marie Claude Addor; Jorieke E H Bergman; Fabrizio Bianchi; Ljubica Boban; Paula Braz; Clara Cavero Carbonell; Miriam Gatt; Martin Haeusler; Agnieszka Kinsner Ovaskainen; Kari Klungsoyr; Jennifer J Kurinczuk; Nathalie Lelong; Karen Luyt; Anna Materna Kiryluk; Olatz Mokoroa; Carmel Mullaney; ...Mais
PUBLICAÇÃO: 2019, FONTE: NEUROEPIDEMIOLOGY, VOLUME: 53, NÚMERO: 3-4
AUTORES: Michele Santoro; Alessio Coi; Ingeborg Barisic; Ester Garne; Marie Claude Addor; Jorieke E H Bergman; Fabrizio Bianchi; Ljubica Boban; Paula Braz; Clara Cavero Carbonell; Miriam Gatt; Martin Haeusler; Agnieszka Kinsner Ovaskainen; Kari Klungsoyr; Jennifer J Kurinczuk; Nathalie Lelong; Karen Luyt; Anna Materna Kiryluk; Olatz Mokoroa; Carmel Mullaney; ...Mais
PUBLICAÇÃO: 2019, FONTE: NEUROEPIDEMIOLOGY, VOLUME: 53, NÚMERO: 3-4
INDEXADO EM:
Scopus
WOS
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8
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; ...Mais
PUBLICAÇÃO: 2018, FONTE: ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, VOLUME: 103, NÚMERO: 1
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; ...Mais
PUBLICAÇÃO: 2018, FONTE: ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, VOLUME: 103, NÚMERO: 1
INDEXADO EM:
WOS
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9
TÃTULO: Epidemiology of septo-optic dysplasia with focus on prevalence and maternal age - A EUROCAT study
AUTORES: Ester Garne; Anke Rissmann; Marie Claude Addor; Ingeborg Barisic; Jorieke Bergman; Paula Braz; Clara Cavero Carbonell; Elizabeth S Draper; Miriam Gatt; Martin Haeusler; Kari Klungsoyr; Jennifer J Kurinczuk; Nathalie Lelong; Karen Luyt; Catherine Lynch; Mary T O'Mahony; Olatz Mokoroa; Vera Nelen; Amanda J Neville; Anna Pierini; ...Mais
PUBLICAÇÃO: 2018, FONTE: EUROPEAN JOURNAL OF MEDICAL GENETICS, VOLUME: 61, NÚMERO: 9
AUTORES: Ester Garne; Anke Rissmann; Marie Claude Addor; Ingeborg Barisic; Jorieke Bergman; Paula Braz; Clara Cavero Carbonell; Elizabeth S Draper; Miriam Gatt; Martin Haeusler; Kari Klungsoyr; Jennifer J Kurinczuk; Nathalie Lelong; Karen Luyt; Catherine Lynch; Mary T O'Mahony; Olatz Mokoroa; Vera Nelen; Amanda J Neville; Anna Pierini; ...Mais
PUBLICAÇÃO: 2018, FONTE: EUROPEAN JOURNAL OF MEDICAL GENETICS, VOLUME: 61, NÚMERO: 9
INDEXADO EM:
WOS
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10
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; ...Mais
PUBLICAÇÃO: 2014, FONTE: AMERICAN JOURNAL OF MEDICAL GENETICS PART A, VOLUME: 164A, NÚMERO: 12
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; ...Mais
PUBLICAÇÃO: 2014, FONTE: AMERICAN JOURNAL OF MEDICAL GENETICS PART A, VOLUME: 164A, NÚMERO: 12