Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Congenital Disorders Expert Group"'
Autor:
Moorthie, Sowmiya, Blencowe, Hannah, Darlison, Matthew W, Gibbons, Stephen, Lawn, Joy E, Mastroiacovo, Pierpaolo, Morris, Joan K, Modell, Bernadette, Congenital Disorders Expert Group
Chromosomal disorders, of which Down syndrome is the most common, can cause multi-domain disability. In addition, compared to the general population, there is a higher frequency of death before the age of five. In many settings, large gaps in data av
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::59f7781899cca3d9702369292ec5c203
Autor:
Moorthie, Sowmiya, Blencowe, Hannah, Darlison, Matthew W, Lawn, Joy, Morris, Joan K, Modell, Bernadette, Congenital Disorders Expert Group, Bittles, AH, Blencowe, H, Christianson, A, Cousens, S, Darlison, MW, Gibbons, S, Hamamy, H, Khoshnood, B, Howson, CP, Lawn, J, Mastroiacovo, P, Modell, B, Moorthie, S, Morris, JK, Mossey, PA, Neville, AJ, Petrou, M, Povey, S, Rankin, J, Schuler-Faccini, L, Wren, C, Yunnis, KA
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::448332bef0f39dffec1f5526fd9091a5
Autor:
Blencowe, Hannah, Moorthie, Sowmiya, Petrou, Mary, Hamamy, Hanan, Povey, Sue, Bittles, Alan, Gibbons, Stephen, Darlison, Matthew, Modell, Bernadette, Congenital Disorders Expert Group
As child mortality rates overall are decreasing, non-communicable conditions, such as genetic disorders, constitute an increasing proportion of child mortality, morbidity and disability. To date, policy and public health programmes have focused on co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::7359fef81128d84f17036485e3d76dd6
https://researchonline.lshtm.ac.uk/id/eprint/4648879/1/Rare-single-gene-disorders.pdf
https://researchonline.lshtm.ac.uk/id/eprint/4648879/1/Rare-single-gene-disorders.pdf
Autor:
Blencowe, Hannah, Moorthie, Sowmiya, Darlison, Matthew W, Gibbons, Stephen, Modell, Bernadette, Congenital Disorders Expert Group
In the absence of intervention, early-onset congenital disorders lead to pregnancy loss, early death, or disability. Currently, lack of epidemiological data from many settings limits the understanding of the burden of these conditions, thus impeding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::e82eb7393c115f67adef5009e1c4a3c0
Autor:
Moorthie, S, Blencowe, H, W Darlison, M, Lawn, JE, Mastroiacovo, P, Morris, JK, Modell, B, Congenital Disorders Expert Group
Congenital disorders are an important cause of pregnancy loss, premature death and life-long disability. A range of interventions can greatly reduce their burden, but the absence of local epidemiological data on their prevalence and the impact of int
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::8363daf01fc283fbd73f5876727f2596
Autor:
Moorthie, Sowmiya, Blencowe, Hannah, W. Darlison, Matthew, Lawn, Joy E., Mastroiacovo, Pierpaolo, Morris, Joan K., Modell, Bernadette, Congenital Disorders Expert Group
Publikováno v:
Journal of Community Genetics; Oct2018, Vol. 9 Issue 4, p347-362, 16p
