M Arambepola
Overview
Explore the profile of M Arambepola including associated specialties, affiliations and a list of published articles.
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Articles
6
Citations
151
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0
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Recent Articles
1.
ODonnell A, Premawardhena A, Arambepola M, Samaranayake R, Allen S, Peto T, et al.
Proc Natl Acad Sci U S A
. 2009 Oct;
106(44):18716-21.
PMID: 19841268
In many Asian populations, the commonest form of severe thalassemia results from the coinheritance of HbE and beta thalassemia. The management of this disease is particularly difficult because of its...
2.
Premawardhena A, Arambepola M, Katugaha N, Weatherall D
Br J Haematol
. 2008 Mar;
141(3):407-10.
PMID: 18341640
Although the beta thalassaemia trait affects millions of people worldwide, there have been no controlled studies to determine whether it is associated with any clinical disability or abnormal physical signs....
3.
ODonnell A, Premawardhena A, Arambepola M, Allen S, Peto T, Fisher C, et al.
Proc Natl Acad Sci U S A
. 2007 May;
104(22):9440-4.
PMID: 17517643
Severe forms of anemia in children in the developing countries may be characterized by different clinical manifestations at particular stages of development. Whether this reflects developmental changes in adaptation to...
4.
Premawardhena A, Fisher C, Olivieri N, De Silva S, Arambepola M, Perera W, et al.
Lancet
. 2005 Oct;
366(9495):1467-70.
PMID: 16243092
Haemoglobin E beta thalassaemia is the commonest form of severe thalassaemia in many Asian countries, but little is known about its natural history, the reasons for clinical diversity, or its...
5.
Premawardhena A, Fisher C, Liu Y, Verma I, De Silva S, Arambepola M, et al.
Blood Cells Mol Dis
. 2003 Jul;
31(1):98-101.
PMID: 12850492
The promoter region of the UDP glucuronosyltransferase 1 gene (UGT1A1) contains a run of thymine-adenine (TA) repeats, usually six (TA)(6). As well as its relationship to Gilbert's syndrome, homozygosity for...
6.
Rochette J, Pointon J, Fisher C, Perera G, Arambepola M, Arichchi D, et al.
Am J Hum Genet
. 1999 Mar;
64(4):1056-62.
PMID: 10090890
Genetic hemochromatosis (GH) is believed to be a disease restricted to those of European ancestry. In northwestern Europe, >80% of GH patients are homozygous for one mutation, the substitution of...