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Swee L Thein

Showing results (1-10 of 18) with videos related to

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Frontiers in Physiology|June 9, 2020
Recent Advances in the Treatment of Sickle Cell DiseaseGabriel Salinas Cisneros, Swee L Thein
British Journal of Haematology|September 10, 2011
Sickle cell nephropathy - a practical approachClaire C Sharpe, Swee L Thein
The Indian Journal of Medical Research|October 18, 2016
World Sickle Cell Day 2016 : A time for appraisalMya S Thein, Swee L Thein
British Journal of Haematology|May 14, 2015
How we treat delayed haemolytic transfusion reactions in patients with sickle cell diseaseKate Gardner, Carolyn Hoppe, Aleksandar Mijovic, et al.
British Journal of Haematology|March 11, 2015
Delayed haemolytic transfusion reaction in adults with sickle cell disease: a 5-year experienceJennifer B Vidler, Kate Gardner, Kenneth Amenyah, et al.
British Journal of Haematology|November 16, 2011
Effects of co-existing α-thalassaemia in sickle cell disease on hydroxycarbamide therapy and circulating nucleic acidsNisha Vasavda, Claire Woodley, Marlene Allman, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|December 15, 2010
A twins heritability study on alpha hemoglobin stabilizing protein (AHSP) expression variabilityMei I Lai, Chad Garner, Jie Jiang, et al.
British Journal of Haematology|March 14, 2012
Renal iron load in sickle cell disease is influenced by severity of haemolysisNisha Vasavda, Lucía Gutiérrez, Michael J House, et al.
British Journal of Haematology|December 17, 2016
Interim assessment of liver damage in patients with sickle cell disease using new non-invasive techniquesEmma Drasar, Emer Fitzpatrick, Kate Gardner, et al.
British Journal of Haematology|June 22, 2010
Outcome of adults with sickle cell disease admitted to critical care - experience of a single institution in the UKKate Gardner, Cathy Bell, Jack L Bartram, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Frontiers in Physiology|June 9, 2020
Recent Advances in the Treatment of Sickle Cell DiseaseGabriel Salinas Cisneros, Swee L Thein
British Journal of Haematology|September 10, 2011
Sickle cell nephropathy - a practical approachClaire C Sharpe, Swee L Thein
The Indian Journal of Medical Research|October 18, 2016
World Sickle Cell Day 2016 : A time for appraisalMya S Thein, Swee L Thein
British Journal of Haematology|May 14, 2015
How we treat delayed haemolytic transfusion reactions in patients with sickle cell diseaseKate Gardner, Carolyn Hoppe, Aleksandar Mijovic, et al.
British Journal of Haematology|March 11, 2015
Delayed haemolytic transfusion reaction in adults with sickle cell disease: a 5-year experienceJennifer B Vidler, Kate Gardner, Kenneth Amenyah, et al.
British Journal of Haematology|November 16, 2011
Effects of co-existing α-thalassaemia in sickle cell disease on hydroxycarbamide therapy and circulating nucleic acidsNisha Vasavda, Claire Woodley, Marlene Allman, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|December 15, 2010
A twins heritability study on alpha hemoglobin stabilizing protein (AHSP) expression variabilityMei I Lai, Chad Garner, Jie Jiang, et al.
British Journal of Haematology|March 14, 2012
Renal iron load in sickle cell disease is influenced by severity of haemolysisNisha Vasavda, Lucía Gutiérrez, Michael J House, et al.
British Journal of Haematology|December 17, 2016
Interim assessment of liver damage in patients with sickle cell disease using new non-invasive techniquesEmma Drasar, Emer Fitzpatrick, Kate Gardner, et al.
British Journal of Haematology|June 22, 2010
Outcome of adults with sickle cell disease admitted to critical care - experience of a single institution in the UKKate Gardner, Cathy Bell, Jack L Bartram, et al.
Pageof 2