Zobrazeno 1 - 10
of 413
pro vyhledávání: '"B Modell"'
Autor:
C McLeod, N Fleeman, J Kirkham, A Bagust, A Boland, P Chu, R Dickson, Y Dundar, J Greenhalgh, B Modell, A Olujohungbe, P Telfer, T Walley
Publikováno v:
Health Technology Assessment, Vol 13, Iss 1 (2009)
Objectives: To assess the clinical effectiveness and cost-effectiveness of deferasirox for the treatment of iron overload associated with regular blood transfusions in patients with chronic anaemia such as beta-thalassaemia major (beta-TM) and sickle
Externí odkaz:
https://doaj.org/article/74c433c3d22f4ecfb447a76b7a2ef1f4
Publikováno v:
Journal of Community Genetics.
Birth defects, also known as congenital disorders, are a significant health issue impacting at least five million births annually worldwide. For policymakers to mount a relevant healthcare response to care for those affected, the burden of disease of
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
Akademický článek
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Publikováno v:
European Journal of Haematology. 55:103-109
We have studied the prevalence and molecular nature of hereditary anaemias (abnormal haemoglobins, beta-thalassaemia, alpha-thalassaemia, and Glucose 6 phosphate dehydrogenase (G6PD) deficiency) in a primitive central Indian tribe, the Baiga. 43% of
Publikováno v:
Scandinavian Journal of Clinical and Laboratory Investigation. 67:87-96
The high prevalence of microcytosis (defined here as mean cell haemoglobin27 pg) with no other abnormality is a principal cause of confusion in screening for haemoglobin disorders. Here we report the results of a small pilot study aiming to resolve t
Publikováno v:
BT TECHNOL J, 24 (3) 17-32. (2006)
Historically, the healthcare system has not made effective use of information technology. On the face of things, it would seem to provide a natural and richly varied domain in which to target benefit from IT solutions. But history shows that it is on
Autor:
B. Modell, P. H. Reddy
Publikováno v:
Journal of Biosocial Science. 29:19-31
This paper outlines the demographic characteristics of the Baiga tribe, one of the most primitive of the aboriginal tribal groups of Central India. The Baiga population has grown steadily since the first anthropological study of the tribe in the 1930
Autor:
P A, Mossey, B, Modell
Publikováno v:
Frontiers of oral biology. 16
Classical descriptive epidemiology in the field of cleft lip and palate aims to quantify the problem, and in the higher income countries it is possible to do this with varying degrees of accuracy. This is not however possible in every country in the
Autor:
S. Smidt-Jensen, Bruno Brambati, George G. Rhoads, B. Modell, P. Ammala, Yury Verlinsky, Norman A. Ginsberg, Yves Dumez, J. Simpson, L. Jackson, U. Froster, Wolfgang Holzgreve, A. M. Kuliev
Publikováno v:
Prenatal Diagnosis. 13:197-209