Zobrazeno 1 - 10
of 137
pro vyhledávání: '"C. de Vigan"'
Publikováno v:
BJOG: An International Journal of Obstetrics & Gynaecology. 115:1087-1095
Objective To assess long-term trends in disparities for prenatal diagnosis of Down syndrome in relation to policy changes. Design Population-based observational study. Setting Paris. Population Residents of Paris who gave birth or had a termination o
Publikováno v:
Gynécologie Obstétrique & Fertilité. 36:146-150
Resume Objectifs Evaluer les tendances recentes de la prevalence de la trisomie 21 et du pourcentage de cas avec diagnostic prenatal dans la population parisienne. Patientes et methodes Quatre cent quatre-vingt-dix-neuf cas de trisomie 21 ont ete enr
Autor:
François Goffinet, A. Lhomme, Béatrice Blondel, V. Vodovar, M. Garel, C. De Vigan, Babak Khoshnood
Publikováno v:
Ultrasound in Obstetrics and Gynecology = Ultrasound in Obstetrics & Gynecology
Ultrasound in Obstetrics and Gynecology = Ultrasound in Obstetrics & Gynecology, 2006, 28 (3), pp.242-8. ⟨10.1002/uog.2845⟩
Ultrasound in Obstetrics and Gynecology = Ultrasound in Obstetrics & Gynecology, Wiley-Blackwell, 2006, 28 (3), pp.242-8. ⟨10.1002/uog.2845⟩
Ultrasound in Obstetrics and Gynecology = Ultrasound in Obstetrics & Gynecology, 2006, 28 (3), pp.242-8. ⟨10.1002/uog.2845⟩
Ultrasound in Obstetrics and Gynecology = Ultrasound in Obstetrics & Gynecology, Wiley-Blackwell, 2006, 28 (3), pp.242-8. ⟨10.1002/uog.2845⟩
Objective To assess the effects of sociodemographic and health-provider factors on women's understanding of abnormal results on measurement of nuchal translucency (NT) and maternal serum screening (MSS), 18 months after the implementation of a policy
Autor:
H. Jordan, D. Lillis, C. De Vigan, Maria Loane, Blanca Gener, Ester Garne, Fabrizio Bianchi, Claude Stoll, H. E. K. De Walle, Annette Queisser-Luft, Maria Feijoo, Martin Haeusler, Marie-Claude Addor, David Tucker, Helen Dolk
Publikováno v:
ResearcherID
Scopus-Elsevier
Revue d epidemiologie et de sante publique, 53, 2S87-2S95
Dolk, H, Loane, M, Garne, E, De Walle, H, Queisser-Luft, A, De Vigan, C, Addor, M C, Gener, B, Haeusler, M, Jordan, H, Tucker, D, Stoll, C, Feijoo, M, Lillis, D & Bianchi, F 2005, ' Trends and geographic inequalities in the prevalence of Down syndrome in Europe, 1980-1999 ', Revue d'Epidemiologie et de Sante Publique, vol. 53, no. 2, pp. 87-95 .
Scopus-Elsevier
Revue d epidemiologie et de sante publique, 53, 2S87-2S95
Dolk, H, Loane, M, Garne, E, De Walle, H, Queisser-Luft, A, De Vigan, C, Addor, M C, Gener, B, Haeusler, M, Jordan, H, Tucker, D, Stoll, C, Feijoo, M, Lillis, D & Bianchi, F 2005, ' Trends and geographic inequalities in the prevalence of Down syndrome in Europe, 1980-1999 ', Revue d'Epidemiologie et de Sante Publique, vol. 53, no. 2, pp. 87-95 .
Background EUROCAT is a network of population-based registries for the epidemiologic surveillance of congenital anomalies covering approximately one quarter of births in the European Union. Down syndrome constitutes approximately 8% of cases of regis
Publikováno v:
Journal de Gynécologie Obstétrique et Biologie de la Reproduction. 34:8-16
Journal de Gynecologie Obstetrique et Biologie de la Reproduction - Vol. 34 - N° 1-C1 - p. 8-16
Autor:
Yves Gillerot, Vera Nelen, Claude Stoll, Anna Pierini, R. Tincheva, Marie-Claude Addor, Gioacchino Scarano, Ingeborg Barišić, Annette Queisser-Luft, E. Garne, C. De Vigan, Maria Feijoo, David Tucker, Miriam Gatt, Blanca Gener, Helen Dolk, C. Rösch, C. Mosquera, Maria Loane
Publikováno v:
Ultrasound in Obstetrics and Gynecology. 25:6-11
Objectives To assess at a population-based level the frequency with which severe structural congenital malformations are detected prenatally in Europe and the gestational age at detection, and to describe regional variation in these indicators. Metho
Autor:
Pa Boyd, Neus Baena, Diana Wellesley, Claude Stoll, C. De Vigan, Maurizio Clementi, E. Cariati
Publikováno v:
Annales de Génétique. 47:373-380
The objective of this study was to evaluate the contribution of ultrasound scanning to the prenatal detection of trisomy 21 in a large unselected European population. Data from 19 congenital malformation registers in 11 European countries were includ
Autor:
C. De Vigan, E. Cariati, Claude Stoll, Maurizio Clementi, María Rosa Caballín, Miriam Guitart, Neus Baena
Publikováno v:
American Journal of Medical Genetics Part A. :16-20
This study evaluated the prenatal diagnosis of Turner syndrome by ultrasound examination in an unselected population from all over Europe. Data from 19 congenital malformation registries from 11 European countries were analyzed. Turner syndrome was d
Publikováno v:
Prenatal Diagnosis. 19:1113-1118
The results and limitations of current French practices for prenatal diagnosis (PND) of trisomy 21 were examined, using population-based data from the Paris Registry for 1992-97 (219 000 births). Of 670 cases of trisomy 21 reported, 71.0 per cent wer
Autor:
Elisa Calzolari, C. De Vigan, H. E. K. De Walle, Ségolène Aymé, Fabrizio Bianchi, Robin P. Knill-Jones, J. Goujard, Sylvaine Cordier
Publikováno v:
Journal of Clinical Epidemiology. 52:977-982
A drug utilization study was performed using data of the OECM study on Occupational Exposures and Congenital Malformations, which was conducted in six European Registries of Congenital Anomalies (two in France, two in Italy, one in Great Britain, and