Zobrazeno 1 - 10
of 146
pro vyhledávání: '"EUROCAT"'
Publikováno v:
Clinical Epidemiology, Vol Volume 12, Pp 1371-1380 (2020)
Anne Broe,1,2 Per Damkier,1,2 Anton Pottegård,3 Jesper Hallas,1,3 Mette Bliddal3,4 1Department of Clinical Biochemistry and Pharmacology, Odense University Hospital, Odense, Denmark; 2Department of Clinical Research, University of Southern Denmark,
Externí odkaz:
https://doaj.org/article/820d6f16ecde41c8b13bc2ae481a2957
Autor:
Marlene E. Toxværd, Ester Garne
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Surveillance of congenital anomalies is important in order to detect negative influences from environment, medication, or lifestyle as early as possible. Since most teratogens are associated with a spectrum of birth defects rather than a single defec
Externí odkaz:
https://doaj.org/article/3299325e821e4bab8804314ef90493f5
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:
Joan K. Morris, Diana Wellesley, Elizabeth Limb, Jorieke E. H. Bergman, Agnieszka Kinsner‐Ovaskainen, Marie Claude Addor, Jennifer M. Broughan, Clara Cavero‐Carbonell, Carlos M. Dias, Luis‐Javier Echevarría‐González‐de‐Garibay, Miriam Gatt, Martin Haeusler, Ingeborg Barisic, Kari Klungsoyr, Nathalie Lelong, Anna Materna‐Kiryluk, Amanda Neville, Vera Nelen, Mary T. O'Mahony, Isabelle Perthus, Anna Pierini, Judith Rankin, Anke Rissmann, Florence Rouget, Geraldine Sayers, Sarah Stevens, David Tucker, Ester Garne
Publikováno v:
Birth defects research, 114(20), 1417-1426. Wiley
Birth Defects Research
r-FISABIO. Repositorio Institucional de Producción Científica
instname
Birth Defects Research
r-FISABIO. Repositorio Institucional de Producción Científica
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[Corrections added after online publication, 16 November 2022: The last name of Dr. Jennifer M. Broughan was incorrectly spelled in the initial publication. It has been corrected.] Background: Younger mothers are at a greater risk of having a pregnan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c102c9464c324fb641783ed33d64ecdc
https://research.rug.nl/en/publications/65d07439-9406-4c1e-b5e6-1b0283131f71
https://research.rug.nl/en/publications/65d07439-9406-4c1e-b5e6-1b0283131f71
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
Autor:
Eve Blair, Guro L. Andersen, Sarah McIntyre, Kate Himmelmann, Catherine S. Gibson, Shona Goldsmith, Hayley Smithers-Sheedy, Nadia Badawi, Ester Garne
Publikováno v:
The Comprehensive CA-CP Study Group 2021, ' Congenital anomalies in children with pre-or perinatally acquired cerebral palsy : an international data linkage study ', Developmental Medicine and Child Neurology, vol. 63, no. 4, pp. 413-420 . https://doi.org/10.1111/dmcn.14602
Members of the Comprehensive CA-CP study group: Paula Braz and Daniel Virella, Portugal. Departamento de Epidemiologia do INSA Aim: To describe the frequency and types of major congenital anomalies present in children with pre- or perinatally acquire
Autor:
Ingeborg Barisic, Michel Guo, Florence Rouget, Awi Wiesel, Mary O'Mahony, Kari Klungsøyr, Martin Haeusler, Karen Luyt, Maria Loane, Nel Roeleveld, Babak Khoshnood, Diana Wellesley, Bruno Schaub, Han G. Brunner, Jenny J. Kurinczuk, Carmel Mullaney, Clara Cavero-Carbonell, Judith Rankin, Jorieke E. H. Bergman, Monica Lanzoni, Iris A.L.M. van Rooij, Hanitra Randrianaivo, Carlos Matias Dias, Isabelle Perthus, Anna Latos-Bielenska, Natalya Zymak-Zakutnia, Romy van de Putte, Larraitz Etxebarriarteun, Marie-Claude Addor, Elizabeth S Draper, Carlo Marcelis, Hermien E. K. de Walle, Anna Pierini, Amanda J. Neville, Anke Rissmann, Vera Nelen, David Tucker, Nicola Miller, Miriam Gatt
Publikováno v:
PEDIATRIC RESEARCH
r-FISABIO. Repositorio Institucional de Producción Científica
instname
Pediatric Research
van de Putte, R, van Rooij, I A L M, Marcelis, C L M, Guo, M, Brunner, H G, Addor, M-C, Cavero-Carbonell, C, Dias, C M, Draper, E S, Etxebarriarteun, L, Gatt, M, Haeusler, M, Khoshnood, B, Klungsoyr, K, Kurinczuk, J J, Lanzoni, M, Latos-Bielenska, A, Luyt, K, O'Mahony, M T, Miller, N, Mullaney, C, Nelen, V, Neville, A J, Perthus, I, Pierini, A, Randrianaivo, H, Rankin, J, Rissmann, A, Rouget, F, Schaub, B, Tucker, D, Wellesley, D, Wiesel, A, Zymak-Zakutnia, N, Loane, M, Barisic, I, de Walle, H E K, Roeleveld, N & Bergman, J E H 2019, ' Spectrum of congenital anomalies among VACTERL cases : a EUROCAT population-based study ', Pediatric Research . https://doi.org/10.1038/s41390-019-0561-y
Pediatric Research, 87(3), 541-549. Nature Publishing Group
Pediatric Research, 2020, 87 (3), pp.541-549. ⟨10.1038/s41390-019-0561-y⟩
Pediatric Research, Nature Publishing Group, 2020, 87 (3), pp.541-549. ⟨10.1038/s41390-019-0561-y⟩
Pediatric Research, 87, 3, pp. 541-549
r-FISABIO: Repositorio Institucional de Producción Científica
Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (FISABIO)
Pediatric Research, 87, 541-549
r-FISABIO. Repositorio Institucional de Producción Científica
instname
Pediatric Research
van de Putte, R, van Rooij, I A L M, Marcelis, C L M, Guo, M, Brunner, H G, Addor, M-C, Cavero-Carbonell, C, Dias, C M, Draper, E S, Etxebarriarteun, L, Gatt, M, Haeusler, M, Khoshnood, B, Klungsoyr, K, Kurinczuk, J J, Lanzoni, M, Latos-Bielenska, A, Luyt, K, O'Mahony, M T, Miller, N, Mullaney, C, Nelen, V, Neville, A J, Perthus, I, Pierini, A, Randrianaivo, H, Rankin, J, Rissmann, A, Rouget, F, Schaub, B, Tucker, D, Wellesley, D, Wiesel, A, Zymak-Zakutnia, N, Loane, M, Barisic, I, de Walle, H E K, Roeleveld, N & Bergman, J E H 2019, ' Spectrum of congenital anomalies among VACTERL cases : a EUROCAT population-based study ', Pediatric Research . https://doi.org/10.1038/s41390-019-0561-y
Pediatric Research, 87(3), 541-549. Nature Publishing Group
Pediatric Research, 2020, 87 (3), pp.541-549. ⟨10.1038/s41390-019-0561-y⟩
Pediatric Research, Nature Publishing Group, 2020, 87 (3), pp.541-549. ⟨10.1038/s41390-019-0561-y⟩
Pediatric Research, 87, 3, pp. 541-549
r-FISABIO: Repositorio Institucional de Producción Científica
Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (FISABIO)
Pediatric Research, 87, 541-549
Background The VACTERL (Vertebral anomalies, Anal atresia, Cardiac malformations, Tracheo-Esophageal fistula, Renal anomalies, Limb abnormalities) association is the non-random occurrence of at least three of these congenital anomalies: vertebral, an
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Autor:
Chrysovalanto Mamasoula, Marie‐Claude Addor, Clara Cavero Carbonell, Carlos M. Dias, Luis‐Javier Echevarría‐González‐de‐Garibay, Miriam Gatt, Babak Khoshnood, Kari Klungsoyr, Kay Randall, Sylvia Stoianova, Martin Haeusler, Vera Nelen, Amanda J. Neville, Isabelle Perthus, Anna Pierini, Bénédicte Bertaut‐Nativel, Anke Rissmann, Florence Rouget, Bruno Schaub, David Tucker, Diana Wellesley, Natalya Zymak‐Zakutnia, Ingeborg Barisic, Hermien E. K. de Walle, Monica Lanzoni, Carmel Mullaney, Lindsay Pennington, Judith Rankin
Publikováno v:
Birth Defects Research
Birth defects research, 114(20), 1404-1416. Wiley
Birth defects research, 114(20), 1404-1416. Wiley
Background: The total prevalence of congenital heart defects (CHDs) varies by populations and over time. Studies that examine trends in the prevalence of CHD in different regions may shed light on our understanding of the occurrence of CHD and the im
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20ac4ab27e43454da1458bf97ad7cc35
https://hdl.handle.net/11250/3040092
https://hdl.handle.net/11250/3040092