Zobrazeno 1 - 10
of 45
pro vyhledávání: '"J. W. Densem"'
Autor:
A Reid, Michele Santoro, David Tucker, Joan K Morris, E Garne, O Mokoroa Carollo, Kari Klungsøyr, Amanda J. Neville, Elizabeth S Draper, Sonja Kiuru-Kuhlefelt, I Scanlon, S K Urhoj, D Akhmedzhanova, Miriam Gatt, Aurora Puccini, Ingeborg Barišić, Anke Rissmann, Guy Thys, E Den Hond, Alessio Coi, Joanne Given, G Astolfi, L R Lutke, Nathalie Lelong, Nathalie Bertille, H. E. K. De Walle, Babak Khoshnood, J. W. Densem, Joachim Tan, Maria Loane, Sue Jordan, Svetlana V. Glinianaia, Oscar Zurriaga, Diana Wellesley, A Heino, C C Carbonell, L Ostapchuk, L B Bonet
Publikováno v:
Loane, M, Given, J E, Tan, J, Reid, A, Akhmedzhanova, D, Astolfi, G, Barišić, I, Bertille, N, Bonet, L B, Carbonell, C C, Carollo, O M, Coi, A, Densem, J, Draper, E, Garne, E, Gatt, M, Glinianaia, S V, Heino, A, Hond, E D, Jordan, S, Khoshnood, B, Kiuru-Kuhlefelt, S, Klungsøyr, K, Lelong, N, Lutke, L R, Neville, A J, Ostapchuk, L, Puccini, A, Rissmann, A, Santoro, M, Scanlon, I, Thys, G, Tucker, D, Urhoj, S K, De Walle, H E K, Wellesley, D, Zurriaga, O & Morris, J K 2021, ' Linking a European cohort of children born with congenital anomalies to vital statistics and mortality records : A EUROlinkCAT study ', PLOS ONE, vol. 16, no. 8, e0256535 . https://doi.org/10.1371/journal.pone.0256535
PLOS ONE
e0256535
PLoS ONE, Vol 16, Iss 8, p e0256535 (2021)
Loane, M, Given, J E, Tan, J, Reid, A, Akhmedzhanova, D, Astolfi, G, Barišić, I, Bertille, N, Bonet, L B, Carbonell, C C, Carollo, O M, Coi, A, Densem, J, Draper, E, Gatt, M, Glinianaia, S V, Heino, A, Hond, E D, Jordan, S, Khoshnood, B, Kiuru-Kuhlefelt, S, Klungsøyr, K, Lelong, N, Lutke, L R, Neville, A J, Ostapchuk, L, Puccini, A, Rissmann, A, Santoro, M, Scanlon, I, Thys, G, Tucker, D, Urhoj, S K, De Walle, H E K, Wellesley, D, Zurriaga, O & Morris, J K 2021, ' Linking a European cohort of children born with congenital anomalies to vital statistics and mortality records : A EUROlinkCAT study ', PLoS ONE, vol. 16, no. 8, e0256535 . https://doi.org/10.1371/journal.pone.0256535
PLoS One
r-FISABIO. Repositorio Institucional de Producción Científica
instname
PLoS ONE, 16(8):e0256535. PUBLIC LIBRARY SCIENCE
PLoS ONE
PLOS ONE
e0256535
PLoS ONE, Vol 16, Iss 8, p e0256535 (2021)
Loane, M, Given, J E, Tan, J, Reid, A, Akhmedzhanova, D, Astolfi, G, Barišić, I, Bertille, N, Bonet, L B, Carbonell, C C, Carollo, O M, Coi, A, Densem, J, Draper, E, Gatt, M, Glinianaia, S V, Heino, A, Hond, E D, Jordan, S, Khoshnood, B, Kiuru-Kuhlefelt, S, Klungsøyr, K, Lelong, N, Lutke, L R, Neville, A J, Ostapchuk, L, Puccini, A, Rissmann, A, Santoro, M, Scanlon, I, Thys, G, Tucker, D, Urhoj, S K, De Walle, H E K, Wellesley, D, Zurriaga, O & Morris, J K 2021, ' Linking a European cohort of children born with congenital anomalies to vital statistics and mortality records : A EUROlinkCAT study ', PLoS ONE, vol. 16, no. 8, e0256535 . https://doi.org/10.1371/journal.pone.0256535
PLoS One
r-FISABIO. Repositorio Institucional de Producción Científica
instname
PLoS ONE, 16(8):e0256535. PUBLIC LIBRARY SCIENCE
PLoS ONE
EUROCAT is a European network of population-based congenital anomaly (CA) registries. Twenty-one registries agreed to participate in the EUROlinkCAT study to determine if reliable information on the survival of children born with a major CA between 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a00076e0e9c5f7550061a62dddc4d33a
https://openaccess.sgul.ac.uk/id/eprint/113562/14/journal.pone.0256535.pdf
https://openaccess.sgul.ac.uk/id/eprint/113562/14/journal.pone.0256535.pdf
Publikováno v:
International Journal of Population Data Science
International Journal of Population Data Science, Vol 3, Iss 2 (2018)
International Journal of Population Data Science, Vol 3, Iss 2 (2018)
BackgroundOver 130,000 children are born in Europe every year with congenital anomalies which are a major cause of infant mortality, childhood morbidity and long-term disability. A European data linkage study (EUROlinkCAT) aims to investigate the hea
Publikováno v:
European journal of epidemiology. 30(11)
BackgroundScan statistics have been used extensively to identify temporal clusters of health events. We describe the temporal cluster detection methodology adopted by the EUROCAT (European Surveillance of Congenital Anomalies) monitoring system.Metho
Autor:
Shanthi Muttukrishna, Joan K. Morris, Lynne M. George, Hilary Watt, Philip G. Knight, J. W. Densem, A. Hacksaw, Nicholas J. Wald
Publikováno v:
Prenatal Diagnosis. 17:285-290
Publikováno v:
Prenatal Diagnosis. 16:691-698
We conducted a study to investigate ethnic group differences in levels of serum markers used in screening for Down's syndrome [serum alpha-fetoprotein (AFP), unconjugated oestriol (uE3), total human chorionic gonadotrophin (hCG), free alpha- and free
Publikováno v:
BJOG: An International Journal of Obstetrics and Gynaecology. 103:407-412
Objective To determine the value of serum screening for Down's syndrome at 8–14 weeks of pregnancy using seven potential serum markers (alpha-fetoprotein, unconjugated oestriol, total human chorionic gonadotrophin (hCG), free α-hCG, free P-hCG, pr
Publikováno v:
Prenatal Diagnosis. 16:143-153
The value of measuring inhibin-A (a beta A dimer) with human chorionic gonadotrophin (total or the sub-units free a-hCG and free beta-hCG separately), alpha-fetoprotein (AFP), and unconjugated oestriol (uE3) was examined to determine the effect on th
Autor:
A M Stephen, A Semmence, F M Fullerton, Nicholas J. Wald, J. W. Densem, R Stone, A Nicolaides-Bouman, C Frost
Publikováno v:
Thorax. 50:1038-1043
BACKGROUND--Observational and short term intervention studies have reported that smokers of low tar cigarettes inhale more deeply (that is, compensate) than those who smoke high tar cigarettes. To quantify this effect a long term randomised trial was
Autor:
J. W. Densem, Nicholas J. Wald
Publikováno v:
Prenatal Diagnosis. 13:1149-1153
Publikováno v:
Prenatal Diagnosis. 13:1047-1050
As part of the Medical Research Council randomized trial of vitamin supplementation in the prevention of neural tube defects (NTDs), maternal serum alpha-fetoprotein (AFP) was available for 19 NTD pregnancies. Each of these was matched with four unaf