Zobrazeno 1 - 10
of 108
pro vyhledávání: '"Clara Cavero Carbonell"'
Autor:
Nathalie Lelong, Babak Khoshnood, David Tucker, Mika Gissler, Maria Loane, Ingeborg Barisic, Miriam Gatt, Kari Klungsoyr, Amanda Neville, Anna Pierini, Anke Rissmann, Oscar Zurriaga, Joan K Morris, Paula Braz, Vera Nelen, Judith Rankin, Ester Garne, Sue Jordan, Anna Heino, Silvia Baldacci, Michele Santoro, Alessio Coi, Lorena Mezzasalma, Daniel Thayer, Svetlana V Glinianaia, Hermien de Walle, Guy Thys, Anna Latos-Bielenska, Aurora Puccini, Elisa Ballardini, Wladimir Wertelecki, Carlos Matias Dias, Gianni Astolfi, James Densem, Joachim Tan, Joanne Emma Given, Hugh Claridge, Abigail Reid, Liz Limb, Gillian Briggs, Nicholas Connor, Stine Kjaer Urhoj, Mads Damkjær, Christina Neergaard Pedersen, Annarita Armaroli, Ljubica Boban, L Renée Lutke, Nicole H A Siemensma-Mühlenberg, Nathalie Bertille, Makan Rahshenas, Clara Cavero Carbonell, Laia Barrachina Bonet, Laura García Villodre, Anna Jamry-Dziurla, Sonja Kiuru-Kuhlefelt, Lyubov Yevtushok, Nataliia Zymak-Zakutnia, Diana Akhmedzhanova, Lyubov Ostapchuk, Oksana Tsizh, Serhii Lapchenko, Ausenda Machado, Ana João Santos, Liliana Antunes, Hanitra Randrianaivo-Ranjatoelina, Elly Den Hond, Olatz Mokoroa Carollo, Ieuan Scanlon
Publikováno v:
BMJ Open, Vol 11, Iss 6 (2021)
Introduction Congenital anomalies (CAs) are a major cause of infant mortality, childhood morbidity and long-term disability. Over 130 000 children born in Europe every year will have a CA. This paper describes the EUROlinkCAT study, which is investig
Externí odkaz:
https://doaj.org/article/71d0d10a7c8340b8864daf7f71f7e0a9
Autor:
Monica Mazzucato, Laura Visonà Dalla Pozza, Paola Facchin, Cèline Angin, Francis Agius, Clara Cavero-Carbonell, Virginia Corrochano, Katerina Hanusova, Kurt Kirch, Deborah Lambert, Caterina Lucano, Sylvie Maiella, Monica Panzaru, Cristina Rusu, Stefanie Weber, Oscar Zurriaga, Miroslav Zvolsky, Ana Rath
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-10 (2023)
Abstract Background Estimates of rare disease (RD) population impact in terms of number of affected patients and accurate disease definition is hampered by their under-representation in current coding systems. This study tested the use of a specific
Externí odkaz:
https://doaj.org/article/92bdc030169a4604a94410a63f004f43
Autor:
Mads Damkjær, Ester Garne, Maria Loane, Stine K. Urhoj, Elisa Ballardini, Clara Cavero‐Carbonell, Alessio Coi, Laura García‐Villodre, Joanne Given, Mika Gissler, Anna Heino, Sue Jordan, Elizabeth Limb, Amanda J Neville, Anna Pierini, Anke Rissmann, Joachim Tan, Ieuan Scanlon, Joan K Morris
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 12, Iss 24 (2023)
Background The purpose of this study was to evaluate the timing of the first cardiac surgery, the number of cardiac surgeries performed, and 30‐day postoperative mortality rate for children with severe congenital heart defects (sCHDs) in their firs
Externí odkaz:
https://doaj.org/article/ed67b3185a5f457e93cf8a5951905984
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:
Mika Gissler, Susan Jordan, Maria Loane, Anna Pierini, Joan K Morris, Clara Cavero-Carbonell, Ester Garne, Anna Heino, Alessio Coi, Elisa Ballardini, Gianni Astolfi, Joachim Tan, Joanne Emma Given, Stine Kjaer Urhoj, Ieuan Scanlon, Laia Barrachina-Bonet, Natalie Divin
Publikováno v:
BMJ Open, Vol 13, Iss 10 (2023)
Objectives To explore the risk of being prescribed/dispensed medications for respiratory symptoms and breathing difficulties in children with and without congenital anomalies.Design A EUROlinkCAT population-based data linkage cohort study. Data on ch
Externí odkaz:
https://doaj.org/article/0d0d76450de246ac8403efb7eb041017
Autor:
Babak Khoshnood, David Tucker, Susan Jordan, Hanitra Randrianaivo, Maria Loane, Ingeborg Barisic, Miriam Gatt, Kari Klungsoyr, Anna Pierini, Anke Rissmann, Joan K Morris, Clara Cavero-Carbonell, Vera Nelen, Amanda J Neville, Ester Garne, Hermien de Walle, Carlos Dias, Wladimir Wertelecki, Joachim Tan, Hugh Claridge, Sonja Kiuru-Kuhlefelt, Olatz Mokoroa Carollo
Publikováno v:
BMJ Open, Vol 13, Iss 7 (2023)
Introduction Linking healthcare data sets can create valuable resources for research, particularly when investigating rare exposures or outcomes. However, across Europe, the permissions processes required to access data can be complex. This paper doc
Externí odkaz:
https://doaj.org/article/ab83eb18afeb496085e71265b0a01be3
Autor:
Elena Marcus, Anna Latos-Bielenska, Anna Jamry-Dziurla, Ingeborg Barišić, Clara Cavero-Carbonell, Elly Den Hond, Ester Garne, Lucas Genard, Ana João Santos, LRenée Lutke, Carlos Matias Dias, Christina Neergaard Pedersen, Amanda J. Neville, Annika Niemann, Ljubica Odak, Anna Pierini, Juan Rico, Anke Rissmann, Judith Rankin, Joan K. Morris
Publikováno v:
BMC Pediatrics, Vol 22, Iss 1, Pp 1-13 (2022)
Abstract Background Parents of children who have a congenital anomaly can experience significant worry about their child’s health. Access to clear, helpful, and trustworthy information can provide a valuable source of support. In this study the aim
Externí odkaz:
https://doaj.org/article/99e0dbde7f4840a99f1d48ef77f06a74
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:
Lucía Páramo-Rodríguez, Clara Cavero-Carbonell, Sandra Guardiola-Vilarroig, Aurora López-Maside, M. Eugenia González Sanjuán, Óscar Zurriaga
Publikováno v:
Gaceta Sanitaria, Vol 37, Iss , Pp 102272- (2023)
Resumen: Objetivo: Describir el impacto de la demora diagnóstica de enfermedades raras y analizar las necesidades psicosociales de las personas afectadas en relación con dicha demora. Método: Se ha empleado el enfoque cualitativo mediante la reali
Externí odkaz:
https://doaj.org/article/4000f5d39d8840c59f54d55603062c4e
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