Survey of prenatal screening policies in Europe for structural malformations and chromosome anomalies, and their impact on detection and termination rates for neural tube defects a...

por Boyd, PA, DeVigan, C, Khoshnood, B, Loane, M, Garne, E, Dolk, H
Publicado 2008

Colorectal cancer screening: factors associated with colonoscopy after a positive faecal occult blood test

por Ferrat, E, Le Breton, J, Veerabudun, K, Bercier, S, Brixi, Z, Khoshnood, B, Paillaud, E, Attali, C, Bastuji-Garin, S
Publicado 2013

Estimating the birth prevalence and pregnancy outcomes of congenital malformations worldwide

por Moorthie, Sowmiya, Blencowe, Hannah, Darlison, Matthew W., Lawn, Joy, Morris, Joan K., Modell, Bernadette, Bittles, A. H., Blencowe, H., Christianson, A., Cousens, S., Darlison, M. W., Gibbons, S., Hamamy, H., Khoshnood, B., Howson, C. P., Lawn, J., Mastroiacovo, P., Modell, B., Moorthie, S., Morris, J. K., Mossey, P. A., Neville, A. J., Petrou, M., Povey, S., Rankin, J., Schuler-Faccini, L., Wren, C., Yunnis, K. A.
Publicado 2018

Linking a European cohort of children born with congenital anomalies to vital statistics and mortality records: A EUROlinkCAT study

por 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. Mokoroa, Coi, A., Densem, J., Draper, E., Garne, E., Gatt, M., Glinianaia, S. V., Heino, A., Hond, E. Den, 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.
Publicado 2021