Zobrazeno 1 - 10
of 81
pro vyhledávání: '"Hermien E K de Walle"'
Autor:
Mika Gissler, Maria Loane, Ingeborg Barisic, Hermien E K de Walle, Miriam Gatt, Kari Klungsoyr, Anna Pierini, Anke Rissmann, Oscar Zurriaga, Diana G Wellesley, Clara Cavero-Carbonell, Olatz Mokoroa, Judith Rankin, Ester Garne, Sue Jordan, Anna Heino, Michele Santoro, Alessio Coi, Joan Morris, Svetlana V Glinianaia, Elisa Ballardini, Joachim Tan, Abigail Reid, Stine Kjaer Urhoj, Lyubov Yevtushok, Diana Akhmedzhanova, Joanne Given, Amanda Julie Neville, Amaia Aizpurua, Renee Lutke, Daniel S Thayer
Publikováno v:
BMJ Paediatrics Open, Vol 7, Iss 1 (2023)
Background Congenital anomalies (CAs) increase the risk of death during infancy and childhood. This study aimed to evaluate the accuracy of using death certificates to estimate the burden of CAs on mortality for children under 10 years old.Methods Ch
Externí odkaz:
https://doaj.org/article/f42c5f88e93644388fcf44d53460a7f0
Autor:
Maria Loane, Joanne E Given, Joachim Tan, Ingeborg Barišić, Laia Barrachina-Bonet, Clara Cavero-Carbonell, Alessio Coi, James Densem, Ester Garne, Mika Gissler, Anna Heino, Sue Jordan, Renee Lutke, Amanda J Neville, Ljubica Odak, Aurora Puccini, Michele Santoro, Ieuan Scanlon, Stine K Urhoj, Hermien E K de Walle, Diana Wellesley, Joan K Morris
Publikováno v:
PLoS ONE, Vol 18, Iss 8, p e0290711 (2023)
Linking routinely collected healthcare administrative data is a valuable method for conducting research on morbidity outcomes, but linkage quality and accuracy needs to be assessed for bias as the data were not collected for research. The aim of this
Externí odkaz:
https://doaj.org/article/51d2e01c72be47beb5dae90517d25667
Autor:
Stine Kjaer Urhoj, Joachim Tan, Joan K Morris, Joanne Given, Gianni Astolfi, Silvia Baldacci, Ingeborg Barisic, Joanna Brigden, Clara Cavero-Carbonell, Hannah Evans, Mika Gissler, Anna Heino, Sue Jordan, Renée Lutke, Ljubica Odak, Aurora Puccini, Michele Santoro, Ieuan Scanlon, Hermien E K de Walle, Diana Wellesley, Óscar Zurriaga, Maria Loane, Ester Garne
Publikováno v:
PLoS ONE, Vol 17, Iss 7, p e0269874 (2022)
BackgroundCongenital anomalies are a leading cause of childhood morbidity, but little is known about the long-term outcomes.ObjectiveTo quantify the burden of disease in childhood for children with congenital anomalies by assessing the risk of hospit
Externí odkaz:
https://doaj.org/article/725dcc662514441a9a6a7aa5ffbc4093
Autor:
Alessio Coi, Michele Santoro, Anna Pierini, Judith Rankin, Svetlana V. Glinianaia, Joachim Tan, Abigail-Kate Reid, Ester Garne, Maria Loane, Joanne Given, Elisa Ballardini, Clara Cavero-Carbonell, Hermien E. K. de Walle, Miriam Gatt, Laura García-Villodre, Mika Gissler, Sue Jordan, Sonja Kiuru-Kuhlefelt, Stine Kjaer Urhoj, Kari Klungsøyr, Nathalie Lelong, L. Renée Lutke, Amanda J. Neville, Makan Rahshenas, Ieuan Scanlon, Diana Wellesley, Joan K. Morris
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-11 (2022)
Abstract Background Congenital anomalies are the leading cause of perinatal, neonatal and infant mortality in developed countries. Large long-term follow-up studies investigating survival beyond the first year of life in children with rare congenital
Externí odkaz:
https://doaj.org/article/dd08c0e1b5574f08bdb9c7543519f4b7
Autor:
Eline A. Verberne, Shirley M. Lo‐A‐Njoe, Manon van Ginkel, Jet Zwolsman, Sylke Nikkels, Lauren Clement, Maartje de Vroomen, Maria L. G. Wever, Eric Arends, Hilda Holtsema, Petra J. Hajenius, Daphne Moreta, Ginette M. Ecury‐Goossen, Marcel M. A. M. Mannens, Hermien E. K. de Walle, Jorieke E. H. Bergman, Mieke M. van Haelst
Publikováno v:
Birth defects research. John Wiley and Sons Ltd
Birth defects research, 115(6), 595-604. John Wiley and Sons Ltd
Verberne, E A, Lo-A-Njoe, S M, van Ginkel, M, Zwolsman, J, Nikkels, S, Clement, L, de Vroomen, M, Wever, M L G, Arends, E, Holtsema, H, Hajenius, P J, Moreta, D, Ecury-Goossen, G M, Mannens, M M A M, de Walle, H E K, Bergman, J E H & van Haelst, M M 2023, ' Prevalence of congenital anomalies in the Dutch Caribbean islands of Aruba, Bonaire, and Curaçao ', Birth defects research, vol. 115, no. 6, pp. 595-604 . https://doi.org/10.1002/bdr2.2153, https://doi.org/10.1002/bdr2.2153
Birth defects research, 115(6), 595-604. John Wiley and Sons Ltd
Verberne, E A, Lo-A-Njoe, S M, van Ginkel, M, Zwolsman, J, Nikkels, S, Clement, L, de Vroomen, M, Wever, M L G, Arends, E, Holtsema, H, Hajenius, P J, Moreta, D, Ecury-Goossen, G M, Mannens, M M A M, de Walle, H E K, Bergman, J E H & van Haelst, M M 2023, ' Prevalence of congenital anomalies in the Dutch Caribbean islands of Aruba, Bonaire, and Curaçao ', Birth defects research, vol. 115, no. 6, pp. 595-604 . https://doi.org/10.1002/bdr2.2153, https://doi.org/10.1002/bdr2.2153
Background: Congenital anomalies represent an important global health issue. Data on the prevalence and pattern of congenital anomalies in the Caribbean region are scarce and lacking altogether in Aruba, Bonaire and Curaçao (ABC islands). Methods: W
Autor:
Jorieke E. H. Bergman, Ingeborg Barišić, Marie‐Claude Addor, Paula Braz, Clara Cavero‐Carbonell, Elizabeth S. Draper, Luis J. Echevarría‐González‐de‐Garibay, Miriam Gatt, Martin Haeusler, Babak Khoshnood, Kari Klungsøyr, Jennifer J. Kurinczuk, Anna Latos‐Bielenska, Karen Luyt, Danielle Martin, Carmel Mullaney, Vera Nelen, Amanda J. Neville, Mary T. O'Mahony, Isabelle Perthus, Anna Pierini, Hanitra Randrianaivo, Judith Rankin, Anke Rissmann, Florence Rouget, Gerardine Sayers, Bruno Schaub, Sarah Stevens, David Tucker, Christine Verellen‐Dumoulin, Awi Wiesel, Erica H. Gerkes, Annie Perraud, Maria A. Loane, Diana Wellesley, Hermien E. K. de Walle
Publikováno v:
American Journal of Medical Genetics. Part A.
American Journal of Medical Genetics. Part A, 191(4), 995-1006. Wiley
Bergman, J E H, Barišić, I, Addor, M C, Braz, P, Cavero-Carbonell, C, Luyt, K & et, A 2022, ' Amniotic band syndrome and limb body wall complex in Europe 1980–2019 ', American Journal of Medical Genetics . https://doi.org/10.1002/ajmg.a.63107
American Journal of Medical Genetics. Part A
American Journal of Medical Genetics. Part A, 191(4), 995-1006. Wiley
Bergman, J E H, Barišić, I, Addor, M C, Braz, P, Cavero-Carbonell, C, Luyt, K & et, A 2022, ' Amniotic band syndrome and limb body wall complex in Europe 1980–2019 ', American Journal of Medical Genetics . https://doi.org/10.1002/ajmg.a.63107
American Journal of Medical Genetics. Part A
Amniotic band syndrome (ABS) and limb body wall complex (LBWC) have an overlapping phenotype of multiple congenital anomalies and their etiology is unknown. We aimed to determine the prevalence of ABS and LBWC in Europe from 1980 to 2019and to descri
Autor:
Aizati N. A. Daud, Eefke L. Bergsma, Jorieke E. H. Bergman, Hermien E. K. De Walle, Wilhelmina S. Kerstjens-Frederikse, Bert J. Bijker, Eelko Hak, Bob Wilffert
Publikováno v:
BMC Pregnancy and Childbirth, Vol 17, Iss 1, Pp 1-9 (2017)
Abstract Background Pharmacogenetics is an emerging field currently being implemented to improve safety when prescribing drugs. While many women who take drugs during pregnancy would likely benefit from such personalized drug therapy, data is lacking
Externí odkaz:
https://doaj.org/article/ef02c2eb0d244cb493ae162be62f9bbd
Autor:
Svetlana V Glinianaia, Judith Rankin, Joachim Tan, Maria Loane, Ester Garne, Clara Cavero-Carbonell, Hermien E K de Walle, Miriam Gatt, Mika Gissler, Kari Klungsøyr, Natalie Lelong, Amanda Neville, Anna Pierini, David F Tucker, Stine Kjaer Urhoj, Diana Gay Wellesley, Joan K Morris
Publikováno v:
Archives of Disease in Childhood
ObjectiveTo investigate the survival to 10 years of age of children with trisomy 13 (T13) and children with trisomy 18 (T18), born 1995–2014.DesignPopulation-based cohort study that linked mortality data to data on children born with T13 or T18, in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::647fa98b0fa8a7c5dcff7284e2219c8a
https://hdl.handle.net/11250/3073344
https://hdl.handle.net/11250/3073344
Autor:
Alessio Coi, Ingeborg Barisic, Ester Garne, Anna Pierini, Marie‐Claude Addor, Amaia Aizpurua Atxega, Elisa Ballardini, Paula Braz, Jennifer M. Broughan, Clara Cavero‐Carbonell, Hermien E. K. de Walle, Elizabeth S. Draper, Miriam Gatt, Martin Häusler, Agnieszka Kinsner‐Ovaskainen, Jennifer J. Kurinczuk, Nathalie Lelong, Karen Luyt, Lorena Mezzasalma, Carmel Mullaney, Vera Nelen, Ljubica Odak, Mary T. O'Mahony, Isabelle Perthus, Hanitra Randrianaivo, Judith Rankin, Anke Rissmann, Florence Rouget, Bruno Schaub, David Tucker, Diana Wellesley, Katarzyna Wiśniewska, Lyubov Yevtushok, Michele Santoro
Publikováno v:
Journal of the European Academy of Dermatology and Venereology
Journal of the European Academy of Dermatology and Venereology, 2022, ⟨10.1111/jdv.18690⟩
JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY
r-FISABIO. Repositorio Institucional de Producción Científica
instname
Journal of the European Academy of Dermatology and Venereology. Wiley
Journal of the European Academy of Dermatology and Venereology, 2022, ⟨10.1111/jdv.18690⟩
JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY
r-FISABIO. Repositorio Institucional de Producción Científica
instname
Journal of the European Academy of Dermatology and Venereology. Wiley
Background Aplasia cutis congenita (ACC) is a rare congenital anomaly characterized by localized or widespread absence of skin at birth, mainly affecting the scalp. Most information about ACC exists as individual case reports and medium-sized studies
Autor:
Carmel Mullaney, Mary O'Mahony, Ingeborg Barišić, Nataliia Zymak-Zakutnia, Martin Haeusler, Bruno Schaub, Olatz Mokoroa, Anna Materna-Kiryluk, David Tucker, Anna Pierini, Ljubica Boban, Miriam Gatt, Clara Cavero-Carbonell, Michele Santoro, Anke Rissmann, Jennifer J Kurinczuk, Alessio Coi, Nathalie Lelong, Kari Klungsøyr, Florence Rouget, Silvia Baldacci, Isabelle Perthus, Hermien E. K. de Walle, Monica Lanzoni, Ester Garne, Vera Nelen, Paula Braz, Elisa Ballardini, Karen Luyt, Marie-Claude Addor, Diana Wellesley, Judith Rankin, Hanitra Randrianaivo, Elizabeth S Draper
Publikováno v:
Santoro, M, Coi, A, Barišić, I, Pierini, A, Addor, M C, Baldacci, S, Ballardini, E, Boban, L, Braz, P, Cavero-Carbonell, C, de Walle, H E K, Draper, E S, Gatt, M, Haeusler, M, Klungsøyr, K, Kurinczuk, J J, Materna-Kiryluk, A, Lanzoni, M, Lelong, N, Luyt, K, Mokoroa, O, Mullaney, C, Nelen, V, O’Mahony, M T, Perthus, I, Randrianaivo, H, Rankin, J, Rissmann, A, Rouget, F, Schaub, B, Tucker, D, Wellesley, D, Zymak-Zakutnia, N & Garne, E 2021, ' Epidemiology of Pierre-Robin sequence in Europe : A population-based EUROCAT study ', Paediatric and Perinatal Epidemiology, vol. 35, no. 5, pp. 530-539 . https://doi.org/10.1111/ppe.12776
Paediatric and Perinatal Epidemiology
Paediatric and Perinatal Epidemiology, 2021, 35 (5), pp.530-539. ⟨10.1111/ppe.12776⟩
Paediatric and Perinatal Epidemiology, Wiley, 2021, 35 (5), pp.530-539. ⟨10.1111/ppe.12776⟩
Santoro, M, Luyt, K, Garne, E & al., E 2021, ' Epidemiology of Pierre-Robin sequence in Europe : a population-based EUROCAT study ', Paediatric and Perinatal Epidemiology, vol. 35, no. 5, pp. 530-539 . https://doi.org/10.1111/ppe.12776
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
PAEDIATRIC AND PERINATAL EPIDEMIOLOGY
r-FISABIO. Repositorio Institucional de Producción Científica
instname
Paediatric and Perinatal Epidemiology, 35(5), 530-539. Wiley
Paediatric and Perinatal Epidemiology
Paediatric and Perinatal Epidemiology, 2021, 35 (5), pp.530-539. ⟨10.1111/ppe.12776⟩
Paediatric and Perinatal Epidemiology, Wiley, 2021, 35 (5), pp.530-539. ⟨10.1111/ppe.12776⟩
Santoro, M, Luyt, K, Garne, E & al., E 2021, ' Epidemiology of Pierre-Robin sequence in Europe : a population-based EUROCAT study ', Paediatric and Perinatal Epidemiology, vol. 35, no. 5, pp. 530-539 . https://doi.org/10.1111/ppe.12776
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
PAEDIATRIC AND PERINATAL EPIDEMIOLOGY
r-FISABIO. Repositorio Institucional de Producción Científica
instname
Paediatric and Perinatal Epidemiology, 35(5), 530-539. Wiley
Background: Pierre Robin sequence (PRS) is a rare congenital anomaly. Respiratory disorders and feeding difficulties represent the main burden. Objective: The aim of this study was to investigate the epidemiology of PRS using a cohort of cases from E