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Browsing by Author Fisher, C.A.

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Showing results 18 to 23 of 23 < previous

Issue Date	Title	Author(s)
2015	Rare hemoglobin variants: Hb G-Szuhu (HBB: c.243C>G), Hb G-Coushatta (HBB: c.68A>C) and Hb Mizuho (HBB:c.206T>C) in Sri Lankan families	Perera, P.S.; Silva, I.; Hapugoda, M.; Wickramarathne, M.N.; Wijesiriwardena, I.; Efremov, D.G.; Fisher, C.A.; Weatherall, D.J.; Premawardhena, A.
2004	Response of jaundice to phenobarbitone in thalassaemic patients co-inheriting Gilbert syndrome	Premawardhena, A.P.; Arambepola, M.; Fisher, C.A.; Oliveiri, N.F.; Weatherall, D.J.
2017	Selective silencing of α-globin by the histone demethylase inhibitor IOX1: A potentially new pathway for treatment of β-thalassemia	Mettananda, S.; Fisher, C.A.; Sloane-Stanley, J.A.; Taylor, S.; Oppermann, U.; Gibbons, R.J.; Higgs, D.R.
2000	Thalassaemia in Sri Lanka: implications for the future health burden of asian populations	de Silva, S.; Fisher, C.A.; Premawardhena, A.P.; Lamabadusuriya, S.P.; Peto, T.E.; Perera, G.; Old, J.M.; Clegg, J.B.; Olivieri, N.F.; Weatherall, D.J.; Sri Lanka Thalassaemia Study Group
2004	Thalassemia in Sri Lanka: a progress report	Premawardhena, A.P.; de Silva, S.; Arambepola, M.; Olivieri, N.; Merson, L.; Muraco, J.; Allen, A.; Fisher, C.A.; Peto, T.; Vichinsky, E.; Weatherall, D.J.
2003	The worldwide prevalence of the UGT-1A1 promoter polymorphism as a contributor for phenotypic variability in thalassaemia	Premawardhena, A.P.; Lilt, Y.T.; Fisher, C.A.; Clegg, J.B.; Weatherall, D.J.

Showing results 18 to 23 of 23 < previous