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of 519
pro vyhledávání: '"MODELL, B."'
Yes
Currently there is no consensus regarding services required to help families with consanguineous marriages manage their increased genetic reproductive risk. Genetic services for communities with a preference for consanguineous marriage in th
Currently there is no consensus regarding services required to help families with consanguineous marriages manage their increased genetic reproductive risk. Genetic services for communities with a preference for consanguineous marriage in th
Externí odkaz:
http://hdl.handle.net/10454/10067
Autor:
Darr, Aliya, Small, Neil A., Ahmad, W.I., Atkin, K., Corry, P.C., Benson, J., Morton, R., Modell, B.
WHO advice suggests a family-centred approach for managing the elevated risk of recessively inherited disorders in consanguineous communities, whilst emerging policy recommends community engagement as an integral component of genetic service developm
Externí odkaz:
http://hdl.handle.net/10454/9779
Autor:
Nacul, L.C., Stewart, A., Alberg, C., Chowdhury, S., Darlison, M.W., Grollman, C., Hall, A., Modell, B., Moorthie, S., Sagoo, G.S., Burton, H.
Publikováno v:
Journal of Public Health, 2014 Jun 01. 36(2), 243-250.
Externí odkaz:
https://www.jstor.org/stable/45158346
Publikováno v:
Journal of Community Genetics; Jun2023, Vol. 14 Issue 3, p241-262, 22p
Autor:
Weatherall, D. J., Old, J. M., Thein, S. L., Wainscoat, J. S., Sharma, H., Emery, A. E. H., Modell, B.
Publikováno v:
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences, 1988 Jun . 319(1194), 249-261.
Externí odkaz:
https://www.jstor.org/stable/2396677
Autor:
Angastiniotis, M. Petrou, M. Loukopoulos, D. Modell, B. Farmakis, D. Englezos, P. Eleftheriou, A.
Hemoglobinopathies are the most common monogenic disorders in humans; among them, thalassemia constitutes a serious medical and public health problem in high prevalence regions, in a geographical zone ranging from the Mediterranean Basin to China. In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::447ff91025e3a0c23c36787ae0926663
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3076759
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3076759
Autor:
Modell, B., Petrou, M., Layton, M., Slater, C., Ward, R. H. T., Rodeck, C., Nicolaides, K., Gibbons, S., Fitches, A., Old, J., Varnavides, Lysandros
Publikováno v:
BMJ: British Medical Journal, 1997 Sep . 315(7111), 779-784.
Externí odkaz:
https://www.jstor.org/stable/25175798
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:
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:
Modell, B.1 (AUTHOR) b.modell@pcps.ucl.ac.uk, Darlison, M.1 (AUTHOR), Birgens, H.2 (AUTHOR), Cario, H.3 (AUTHOR), Faustino, P.4 (AUTHOR), Giordano, P. C.5 (AUTHOR), Gulbis, B.6 (AUTHOR), Hopmeier, P.7 (AUTHOR), Lena‐Russo, D.8 (AUTHOR), Romao, L.4 (AUTHOR), Theodorsson, E.9 (AUTHOR)
Publikováno v:
Scandinavian Journal of Clinical & Laboratory Investigation. Feb2007, Vol. 67 Issue 1, p39-70. 32p. 8 Charts, 1 Graph.