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David J Weatherall

Showing results (61-70 of 74) with videos related to

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Lancet (London, England)|October 30, 2012
Global epidemiology of sickle haemoglobin in neonates: a contemporary geostatistical model-based map and population estimatesFrédéric B Piel, Anand P Patil, Rosalind E Howes, et al.
Acta Haematologica|November 9, 2021
Leg Ulcers: A Report in Patients with Hemoglobin E Beta Thalassemia and Review of the Literature in Severe Beta ThalassemiaVikita Mehta, Abirami Kirubarajan, Amir Sabouhanian, et al.
Nature Reviews. Disease Primers|March 16, 2018
Sickle cell diseaseGregory J Kato, Frédéric B Piel, Clarice D Reid, et al.
Transfusion Medicine (Oxford, England)|January 10, 2020
Transfusion-transmitted hepatitis C: A cluster of cases in transfusion-dependent thalassaemia patients in Sri LankaShiromi Perera, David Bonsall, Madunil A Niriella, et al.
American Journal of Hematology|November 25, 2016
Hepcidin detects iron deficiency in Sri Lankan adolescents with a high burden of hemoglobinopathy: A diagnostic test accuracy studyKatherine Wray, Angela Allen, Emma Evans, et al.
Nature Genetics|October 18, 2005
Negative epistasis between the malaria-protective effects of alpha+-thalassemia and the sickle cell traitThomas N Williams, Tabitha W Mwangi, Sammy Wambua, et al.
Nature Communications|April 7, 2011
The global distribution of the Duffy blood groupRosalind E Howes, Anand P Patil, Frédéric B Piel, et al.
Blood|December 19, 2014
Hepcidin is suppressed by erythropoiesis in hemoglobin E β-thalassemia and β-thalassemia traitEmma Jones, Sant-Rayn Pasricha, Angela Allen, et al.
Blood|April 4, 2009
Iron overload in the Asian communityChun Yu Lok, Alison T Merryweather-Clarke, Vip Viprakasit, et al.
The Lancet. Global Health|November 29, 2021
Survival and complications in patients with haemoglobin E thalassaemia in Sri Lanka: a prospective, longitudinal cohort studyAnuja P Premawardhena, Dileepa Senajith Ediriweera, Amir Sabouhanian, et al.
Pageof 8

Showing results (61-70 of 74) with videos related to

Sort By:
Pageof 8
Lancet (London, England)|October 30, 2012
Global epidemiology of sickle haemoglobin in neonates: a contemporary geostatistical model-based map and population estimatesFrédéric B Piel, Anand P Patil, Rosalind E Howes, et al.
Acta Haematologica|November 9, 2021
Leg Ulcers: A Report in Patients with Hemoglobin E Beta Thalassemia and Review of the Literature in Severe Beta ThalassemiaVikita Mehta, Abirami Kirubarajan, Amir Sabouhanian, et al.
Nature Reviews. Disease Primers|March 16, 2018
Sickle cell diseaseGregory J Kato, Frédéric B Piel, Clarice D Reid, et al.
Transfusion Medicine (Oxford, England)|January 10, 2020
Transfusion-transmitted hepatitis C: A cluster of cases in transfusion-dependent thalassaemia patients in Sri LankaShiromi Perera, David Bonsall, Madunil A Niriella, et al.
American Journal of Hematology|November 25, 2016
Hepcidin detects iron deficiency in Sri Lankan adolescents with a high burden of hemoglobinopathy: A diagnostic test accuracy studyKatherine Wray, Angela Allen, Emma Evans, et al.
Nature Genetics|October 18, 2005
Negative epistasis between the malaria-protective effects of alpha+-thalassemia and the sickle cell traitThomas N Williams, Tabitha W Mwangi, Sammy Wambua, et al.
Nature Communications|April 7, 2011
The global distribution of the Duffy blood groupRosalind E Howes, Anand P Patil, Frédéric B Piel, et al.
Blood|December 19, 2014
Hepcidin is suppressed by erythropoiesis in hemoglobin E β-thalassemia and β-thalassemia traitEmma Jones, Sant-Rayn Pasricha, Angela Allen, et al.
Blood|April 4, 2009
Iron overload in the Asian communityChun Yu Lok, Alison T Merryweather-Clarke, Vip Viprakasit, et al.
The Lancet. Global Health|November 29, 2021
Survival and complications in patients with haemoglobin E thalassaemia in Sri Lanka: a prospective, longitudinal cohort studyAnuja P Premawardhena, Dileepa Senajith Ediriweera, Amir Sabouhanian, et al.
Pageof 8