Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Diana G, Wellesley"'
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:
Anke Rissmann, Diana G Wellesley, Sue Jordan, Silvia Baldacci, Michele Santoro, Joan Morris, Elizabeth Limb, Joanne Given, Joanne Brigden, Laura García-Villodre, Amanda Julie Neville, leuan Scanlon
Publikováno v:
BMJ Paediatrics Open, Vol 6, Iss 1 (2022)
Objective To report and compare the proportion of children with and without congenital anomalies undergoing gastrostomy for tube feeding in their first 5 years.Methods A European, population-based data-linkage cohort study (EUROlinkCAT). Children up
Externí odkaz:
https://doaj.org/article/f9f1d8f3165e4b64aad8402f4813a5fb
Autor:
Michele Santoro, Ester Garne, Alessio Coi, Joachim Tan, Maria Loane, Elisa Ballardini, Clara Cavero-Carbonell, Hermien EK de Walle, Miriam Gatt, Mika Gissler, Sue Jordan, Kari Klungsøyr, Natalie Lelong, Stine Kjaer Urhoj, Diana G Wellesley, Joan K Morris
Publikováno v:
Santoro, M, Garne, E, Coi, A, Tan, J, Loane, M, Ballardini, E, Cavero-Carbonell, C, de Walle, H E, Gatt, M, Gissler, M, Jordan, S, Klungsøyr, K, Lelong, N, Urhoj, S K, Wellesley, D G & Morris, J K 2023, ' Survival, hospitalisation and surgery in children born with Pierre Robin sequence : a European population-based cohort study ', Archives of Disease in Childhood, vol. 108, no. 7 . https://doi.org/10.1136/archdischild-2022-324716
Archives of Disease in Childhood
Archives of Disease in Childhood
ObjectiveTo evaluate survival, hospitalisations and surgical procedures for children born with Pierre Robin sequence (PRS) across Europe.DesignMulticentre population-based cohort study.SettingData on 463 live births with PRS from a population of 4 98
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00c5e27e1fa4abffb12790f68390ecce
https://curis.ku.dk/ws/files/356956106/Fulltext.pdf
https://curis.ku.dk/ws/files/356956106/Fulltext.pdf
Autor:
Stephen C Robson, Lyn S Chitty, Stephen Morris, Talitha Verhoef, Gareth Ambler, Diana G Wellesley, Ruth Graham, Claire Leader, Jane Fisher, John A Crolla
Publikováno v:
Efficacy and Mechanism Evaluation, Vol 4, Iss 1 (2017)
Background: Current pathways for testing fetuses at increased risk of a chromosomal anomaly because of an ultrasound anomaly involve karyotyping after rapid aneuploidy exclusion. Chromosomal microarray (CMA) may detect more clinically significant chr
Externí odkaz:
https://doaj.org/article/9f6f49cd6f084059a762f7c9ecfd3232
Autor:
Ester Garne, Joachim Tan, Maria Loane, Silvia Baldacci, Elisa Ballardini, Joanne Brigden, Clara Cavero-Carbonell, Laura García-Villodre, Mika Gissler, Joanne Given, Anna Heino, Sue Jordan, Elizabeth Limb, Amanda Julie Neville, Anke Rissmann, Michele Santoro, leuan Scanlon, Stine Kjaer Urhoj, Diana G Wellesley, Joan Morris
Publikováno v:
Garne, E, Tan, J, Loane, M, Baldacci, S, Ballardini, E, Brigden, J, Cavero-Carbonell, C, Garcia-Villodre, L, Gissler, M, Given, J, Heino, A, Jordan, S, Limb, E, Neville, A J, Rissmann, A, Santoro, M, Scanlon, I, Urhoj, S K, Wellesley, D G & Morris, J 2022, ' Gastrostomy and congenital anomalies : a European population-based study ', BMJ Paediatrics Open, vol. 6, no. 1, 001526 . https://doi.org/10.1136/bmjpo-2022-001526
BMJ Paediatrics Open
BMJ Paediatrics Open
ObjectiveTo report and compare the proportion of children with and without congenital anomalies undergoing gastrostomy for tube feeding in their first 5 years.MethodsA European, population-based data-linkage cohort study (EUROlinkCAT). Children up to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b34a0d1070e5c277098d1389ee75654e
https://pubmed.ncbi.nlm.nih.gov/36053618
https://pubmed.ncbi.nlm.nih.gov/36053618
Autor:
Jenny, Lord, Dominic J, McMullan, Ruth Y, Eberhardt, Gabriele, Rinck, Susan J, Hamilton, Elizabeth, Quinlan-Jones, Elena, Prigmore, Rebecca, Keelagher, Sunayna K, Best, Georgina K, Carey, Rhiannon, Mellis, Sarah, Robart, Ian R, Berry, Kate E, Chandler, Deirdre, Cilliers, Lara, Cresswell, Sandra L, Edwards, Carol, Gardiner, Alex, Henderson, Simon T, Holden, Tessa, Homfray, Tracy, Lester, Rebecca A, Lewis, Ruth, Newbury-Ecob, Katrina, Prescott, Oliver W, Quarrell, Simon C, Ramsden, Eileen, Roberts, Dagmar, Tapon, Madeleine J, Tooley, Pradeep C, Vasudevan, Astrid P, Weber, Diana G, Wellesley, Paul, Westwood, Helen, White, Michael, Parker, Denise, Williams, Lucy, Jenkins, Richard H, Scott, Mark D, Kilby, Lyn S, Chitty, Matthew E, Hurles, Eamonn R, Maher, Elizabeth, Wilson
Publikováno v:
Prenatal Diagnosis
Lancet (London, England)
Lancet (London, England)
Background Fetal structural anomalies, which are detected by ultrasonography, have a range of genetic causes, including chromosomal aneuploidy, copy number variations (CNVs; which are detectable by chromosomal microarrays), and pathogenic sequence va
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::128f07aba6242d5632b16539941083e5
https://doi.org/10.1530/ey.16.14.14
https://doi.org/10.1530/ey.16.14.14
Autor:
Linden J, Stocker, Diana G, Wellesley, Michael P, Stanton, Rajeswari, Parasuraman, David T, Howe
Publikováno v:
Prenatal diagnosis. 35(2)
The aim of this study was to investigate the incidence of congenital lung malformations over the past 19 years. Congenital lung malformations (CLM) are a heterogeneous group of lung abnormalities. The antenatal diagnosis is important for foetal and n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a49b6f6e81d27fb9c66f83f1691876b4
https://pubmed.ncbi.nlm.nih.gov/25256093
https://pubmed.ncbi.nlm.nih.gov/25256093