Zobrazeno 1 - 10
of 22
pro vyhledávání: '"J K, Morris"'
Autor:
M Loane, J E Given, J Tan, A Reid, D Akhmedzhanova, G Astolfi, I Barišić, N Bertille, L B Bonet, C C Carbonell, O Mokoroa Carollo, A Coi, J Densem, E Draper, E Garne, M Gatt, S V Glinianaia, A Heino, E Den Hond, S Jordan, B Khoshnood, S Kiuru-Kuhlefelt, K Klungsøyr, N Lelong, L R Lutke, A J Neville, L Ostapchuk, A Puccini, A Rissmann, M Santoro, I Scanlon, G Thys, D Tucker, S K Urhoj, H E K de Walle, D Wellesley, O Zurriaga, J K Morris
Publikováno v:
PLoS ONE, Vol 16, Iss 8, p e0256535 (2021)
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://doaj.org/article/1268a025bf444663ae3263bef99d6df6
Autor:
Sowmiya, Moorthie, Hannah, Blencowe, Matthew W, Darlison, Joy, Lawn, Joan K, Morris, Bernadette, Modell, A H, Bittles, H, Blencowe, A, Christianson, S, Cousens, M W, Darlison, S, Gibbons, H, Hamamy, B, Khoshnood, C P, Howson, J, Lawn, P, Mastroiacovo, B, Modell, S, Moorthie, J K, Morris, P A, Mossey, A J, Neville, M, Petrou, S, Povey, J, Rankin, L, Schuler-Faccini, C, Wren, K A, Yunnis
Publikováno v:
Journal of Community Genetics
Congenital anomaly registries have two main surveillance aims: firstly to define baseline epidemiology of important congenital anomalies to facilitate programme, policy and resource planning, and secondly to identify clusters of cases and any other e
Autor:
J K Morris
Publikováno v:
Neonatologie Scan. :25-26
Publikováno v:
Neurogastroenterology & Motility. 29:e13057
Publikováno v:
BJOG : an international journal of obstetrics and gynaecology. 116(8)
To determine the excess risk of non-chromosomal congenital anomaly (NCA) among teenage mothers and older mothers.Population-based prevalence study using data from EUROCAT congenital anomaly registers in 23 regions of Europe in 15 countries, covering
This chapter discusses the link between serum homocysteine and coronary heart disease (CHD). Genetic studies show a moderately higher risk of CHD for a moderately higher level of serum homocysteine. Prospective studies show a positive association bet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::985bd70506c1e7f1825b608a3fbaf0da
https://doi.org/10.1093/acprof:oso/9780198525738.003.0016
https://doi.org/10.1093/acprof:oso/9780198525738.003.0016
Publikováno v:
Prenatal diagnosis. 19(2)
It is recognized that pregnancies with Down syndrome are liable to end in spontaneous fetal loss. It is important to determine the magnitude of this effect so that it can be taken into account when assessing the results of antenatal screening program
Autor:
N J, Wald, J W, Densem, L, George, S, Muttukrishna, P G, Knight, H, Watt, A, Hacksaw, J K, Morris
Publikováno v:
Prenatal diagnosis. 17(3)
Autor:
J. C. Lynn, Karen Rene Romines, K.D. Watenpaugh, Tomich Pk, M.‐M. Horng, A.M. Mulichak, K D Lovasz, J K Morris, Howe Wj, Barry C. Finzel
Publikováno v:
Journal of medicinal chemistry. 38(11)
A unique strategy for the enhancement of secondary binding of an inhibitor to an enzyme has been demonstrated in the design of new human immunodeficiency virus (HIV) protease inhibitors. When the planar benzene ring of a 4-hydroxycoumarin lead compou
Publikováno v:
Recent progress in hormone research. 50
During the development of preovulatory follicles, tonic levels of FSH (and steroid) induce expression of aromatase, the LH receptor, and RII beta in a coordinate manner. Despite the similar temporal increase in steady-state levels of mRNA encoding th