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Browsing by Author "Viprakasit, V."

Browsing by Author "Viprakasit, V."

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  • Premawardhena, A.; Fisher, C.A.; Olivieri, N.F.; de Silva, S.; Arambepola, M.; Perera, W.; O Donnell, A.; Peto, T.E.; Viprakasit, V.; Merson, L.; Muraca, G.; Weatherall, D.J. (Lancet Publishing Group, 2005)
    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 management. We studied 109 Sri ...
  • Lok, C.Y.; Merryweather-Clarke, A.T.; Viprakasit, V.; Chinthammitr, Y.; Srichairatanakool, S.; Limwongse, C.; Oleesky, D.; Robins, A.J.; Hudson, J.; Wai, P.; Premawardhena, A.; de Silva, H.J.; Dassanayake, A.S.; McKeown, C.; Jackson, M.; Gama, R.; Khan, N.; Newman, W.; Banait, G.; Chilton, A.; Wilson-Morkeh, I.; Weatherall, D.J.; Robson, K.J.H. (American Society of Hematology, 2009)
    Hereditary hemochromatosis is an iron overload disorder that can lead to the impairment of multiple organs and is caused by mutations in one or more different genes. Type 1 hemochromatosis is the most common form of the ...

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