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Proceedings of the National Academy of Sciences of the United States of America
|
December 4, 2009
Epistatic interactions between genetic disorders of hemoglobin can explain why the sickle-cell gene is uncommon in the Mediterranean
Bridget S Penman, Oliver G Pybus, David J Weatherall, et al.
British Journal of Haematology
|
January 22, 2011
Optimal management of β thalassaemia intermedia
Ali T Taher, Khaled M Musallam, Maria Domenica Cappellini, et al.
The American Journal of Tropical Medicine and Hygiene
|
April 12, 2007
Southeast Asian ovalocytosis and pregnancy in a malaria-endemic region of Papua New Guinea
Angela O'Donnell, Andrew Raiko, John B Clegg, et al.
Plos Medicine
|
July 23, 2013
Global burden of sickle cell anaemia in children under five, 2010-2050: modelling based on demographics, excess mortality, and interventions
Frédéric B Piel, Simon I Hay, Sunetra Gupta, et al.
British Journal of Haematology
|
November 17, 2006
Globin gene expression in Hb Lepore-BAC transgenic mice
Jackie Sloane-Stanley, Nigel A Roberts, Nancy Olivieri, et al.
British Journal of Haematology
|
April 16, 2008
Studies in haemoglobin E beta-thalassaemia
Nancy F Olivieri, Giulia M Muraca, Angela O'Donnell, et al.
The Lancet. Global Health
|
April 22, 2014
Global migration and the changing distribution of sickle haemoglobin: a quantitative study of temporal trends between 1960 and 2000
Frédéric B Piel, Andrew J Tatem, Zhuojie Huang, et al.
Plos Medicine
|
March 21, 2008
Increased microerythrocyte count in homozygous alpha(+)-thalassaemia contributes to protection against severe malarial anaemia
Freya J I Fowkes, Stephen J Allen, Angela Allen, et al.
Blood Cells, Molecules & Diseases
|
February 8, 2018
Haemoglobin variants, iron status and anaemia in Sri Lankan adolescents with low red cell indices: A cross sectional survey
Rexan Rodrigo, Angela Allen, Aresha Manampreri, et al.
Annals of the New York Academy of Sciences
|
August 18, 2010
Emerging insights in the management of hemoglobin E beta thalassemia
Nancy F Olivieri, Vivekanandan Thayalsuthan, Angela O'Donnell, et al.
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of 8
Search research articles
Search
Showing results (31-40 of 74) with videos related to
Sort By:
Page
of 8
Proceedings of the National Academy of Sciences of the United States of America
|
December 4, 2009
Epistatic interactions between genetic disorders of hemoglobin can explain why the sickle-cell gene is uncommon in the Mediterranean
Bridget S Penman, Oliver G Pybus, David J Weatherall, et al.
British Journal of Haematology
|
January 22, 2011
Optimal management of β thalassaemia intermedia
Ali T Taher, Khaled M Musallam, Maria Domenica Cappellini, et al.
The American Journal of Tropical Medicine and Hygiene
|
April 12, 2007
Southeast Asian ovalocytosis and pregnancy in a malaria-endemic region of Papua New Guinea
Angela O'Donnell, Andrew Raiko, John B Clegg, et al.
Plos Medicine
|
July 23, 2013
Global burden of sickle cell anaemia in children under five, 2010-2050: modelling based on demographics, excess mortality, and interventions
Frédéric B Piel, Simon I Hay, Sunetra Gupta, et al.
British Journal of Haematology
|
November 17, 2006
Globin gene expression in Hb Lepore-BAC transgenic mice
Jackie Sloane-Stanley, Nigel A Roberts, Nancy Olivieri, et al.
British Journal of Haematology
|
April 16, 2008
Studies in haemoglobin E beta-thalassaemia
Nancy F Olivieri, Giulia M Muraca, Angela O'Donnell, et al.
The Lancet. Global Health
|
April 22, 2014
Global migration and the changing distribution of sickle haemoglobin: a quantitative study of temporal trends between 1960 and 2000
Frédéric B Piel, Andrew J Tatem, Zhuojie Huang, et al.
Plos Medicine
|
March 21, 2008
Increased microerythrocyte count in homozygous alpha(+)-thalassaemia contributes to protection against severe malarial anaemia
Freya J I Fowkes, Stephen J Allen, Angela Allen, et al.
Blood Cells, Molecules & Diseases
|
February 8, 2018
Haemoglobin variants, iron status and anaemia in Sri Lankan adolescents with low red cell indices: A cross sectional survey
Rexan Rodrigo, Angela Allen, Aresha Manampreri, et al.
Annals of the New York Academy of Sciences
|
August 18, 2010
Emerging insights in the management of hemoglobin E beta thalassemia
Nancy F Olivieri, Vivekanandan Thayalsuthan, Angela O'Donnell, et al.
Page
of 8