Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

David J Weatherall

Showing results (51-60 of 74) with videos related to

Pageof 8
Sort By:
Plos Medicine|May 27, 2005
An immune basis for malaria protection by the sickle cell traitThomas N Williams, Tabitha W Mwangi, David J Roberts, et al.
Annals of the New York Academy of Sciences|December 13, 2005
Single and combination drug therapy for fetal hemoglobin augmentation in hemoglobin E-beta 0-thalassemia: Considerations for treatmentSylvia T Singer, Frans A Kuypers, Nancy F Olivieri, et al.
Blood|September 25, 2004
UGT1A1 variation and gallstone formation in sickle cell diseaseEden V Haverfield, Colin A McKenzie, Terrence Forrester, et al.
Scientific Reports|April 18, 2013
The distribution of haemoglobin C and its prevalence in newborns in AfricaFrédéric B Piel, Rosalind E Howes, Anand P Patil, et al.
Annals of the New York Academy of Sciences|December 13, 2005
Hemoglobin E-beta-thalassemia: Progress report from the International Study GroupAnuja Premawardhena, Shanthimala De Silver, Mahinda Arambepola, et al.
Journal of Biosocial Science|October 26, 2019
Marriage patterns in Sri Lanka and the prevalence of parental consanguinity in patients with β-thalassaemia: a cross-sectional descriptive analysisAnuja P Premawardhena, Shamila T De Silva, M D Dilith C Goonatilleke, et al.
Plos Medicine|April 12, 2006
The effect of alpha+-thalassaemia on the incidence of malaria and other diseases in children living on the coast of KenyaSammy Wambua, Tabitha W Mwangi, Moses Kortok, et al.
The New England Journal of Medicine|September 2, 2011
A functional element necessary for fetal hemoglobin silencingVijay G Sankaran, Jian Xu, Rachel Byron, et al.
Frontiers in Molecular Biosciences|August 27, 2019
A "One-Stop" Screening Protocol for Haemoglobinopathy Traits and Iron Deficiency in Sri LankaAngela Allen, Shiromi Perera, Luxman Perera, et al.
Scientific Reports|July 14, 2019
Genotype-phenotype association analysis identifies the role of α globin genes in modulating disease severity of β thalassaemia intermedia in Sri LankaShiromi Perera, Angela Allen, Ishari Silva, et al.
Pageof 8

Showing results (51-60 of 74) with videos related to

Sort By:
Pageof 8
Plos Medicine|May 27, 2005
An immune basis for malaria protection by the sickle cell traitThomas N Williams, Tabitha W Mwangi, David J Roberts, et al.
Annals of the New York Academy of Sciences|December 13, 2005
Single and combination drug therapy for fetal hemoglobin augmentation in hemoglobin E-beta 0-thalassemia: Considerations for treatmentSylvia T Singer, Frans A Kuypers, Nancy F Olivieri, et al.
Blood|September 25, 2004
UGT1A1 variation and gallstone formation in sickle cell diseaseEden V Haverfield, Colin A McKenzie, Terrence Forrester, et al.
Scientific Reports|April 18, 2013
The distribution of haemoglobin C and its prevalence in newborns in AfricaFrédéric B Piel, Rosalind E Howes, Anand P Patil, et al.
Annals of the New York Academy of Sciences|December 13, 2005
Hemoglobin E-beta-thalassemia: Progress report from the International Study GroupAnuja Premawardhena, Shanthimala De Silver, Mahinda Arambepola, et al.
Journal of Biosocial Science|October 26, 2019
Marriage patterns in Sri Lanka and the prevalence of parental consanguinity in patients with β-thalassaemia: a cross-sectional descriptive analysisAnuja P Premawardhena, Shamila T De Silva, M D Dilith C Goonatilleke, et al.
Plos Medicine|April 12, 2006
The effect of alpha+-thalassaemia on the incidence of malaria and other diseases in children living on the coast of KenyaSammy Wambua, Tabitha W Mwangi, Moses Kortok, et al.
The New England Journal of Medicine|September 2, 2011
A functional element necessary for fetal hemoglobin silencingVijay G Sankaran, Jian Xu, Rachel Byron, et al.
Frontiers in Molecular Biosciences|August 27, 2019
A "One-Stop" Screening Protocol for Haemoglobinopathy Traits and Iron Deficiency in Sri LankaAngela Allen, Shiromi Perera, Luxman Perera, et al.
Scientific Reports|July 14, 2019
Genotype-phenotype association analysis identifies the role of α globin genes in modulating disease severity of β thalassaemia intermedia in Sri LankaShiromi Perera, Angela Allen, Ishari Silva, et al.
Pageof 8