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Browsing Journal/Magazine Articles by Author "Olivieri, N. F."

Browsing Journal/Magazine Articles by Author "Olivieri, N. F."

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  • Emerging insights in the management of hemoglobin E beta thalassemia 
    Olivieri, N. F.; Thayalsuthan, V.; O Donnell, A.; Premawardhena, A.; Rigobon, C.; Muraca, G.; Fisher, C.; Weatherall, D. J. (Wiley-Blackwell, 2010)
    Globally, hemoglobin (Hb) E beta thalassemia accounts for approximately half the severe forms of beta thalassemia. Because of its wide clinical diversity and the ability of patients with this condition to adapt unusually ...
  • Hemoglobin E-[beta] Thalassemia: Progress Report from the International Study Group 
    Premawardhena, A.; de Silva, S.; Arambepola, M.; Olivieri, N. F.; Vichinsky, E. P.; Merson, L.; Muraco, G.; Allen, A.; Fisher, C.; Peto, T.; Weatherall, D. J. (Wiley-Blackwell, 2005)
    A long-term observational study of Hb E-beta-thalassemia in Sri Lanka is beginning to define some of the genetic and environmental factors that are responsible for its remarkable phenotypic variability. In this population ...
  • Natural history of haemoglobin E/beta thalassaemia: the impact of splenectomy on growth and steady state hemoglobin levels 
    Sharma S.; Premawardhena, A.P.; Fathihu, F.; de Silva, S.; de Silva, L.; Vichinsky, E. P.; Weatherall, D. J.; Olivieri, N. F. (American Society of Hematology, 1999)
  • Studies in haemoglobin E beta-thalassaemia 
    Olivieri, N. F.; Muraca, G. M.; O Donnell, A.; Premawardhena, A.; Fisher, C.; Weatherall, D. J. (Wiley-Blackwell, 2008)
    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 its clinical diversity, or its optimal management. Despite ...

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