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Hemoglobin|July 27, 2007
Ringed sideroblasts found in a girl heterozygous for the initiation codon (ATG-->AGG) beta0-thalassemia mutationIn-Sang Jeon, Ki Lyong Nam
Hemoglobin|July 27, 2007
Genetic origin of Hb D-Los Angeles [beta121(GH4)Glu-->Gln, GAA-->CAA] according to the beta-globin gene cluster haplotypesErol O Atalay, Ayfer Atalay, Emre Ustel, et al.
Hemoglobin|June 8, 2010
The 18th ICOC Proceedings in Athens, Greece: New breakthrough in thalassemia leading to the complete treatment of iron overload and to hundreds of patients achieving and maintaining normal body iron stores. Ethical questions on chelation therapyGeorge J Kontoghiorghes
Hemoglobin|June 8, 2010
Maintenance of normal range body iron store levels for up to 4.5 years in thalassemia major patients using deferiprone monotherapyAnnita Kolnagou, George J Kontoghiorghes
Hemoglobin|June 8, 2010
Iron overload, cardiac and other factors affecting pregnancy in thalassemia majorMaria Tsironi, Markissia Karagiorga, Athanasios Aessopos
Hemoglobin|June 8, 2010
Which psychosocial factors are related to chelation adherence in thalassemia? A systematic reviewMichael Evangeli, Kulsoom Mughal, John B Porter
Hemoglobin|June 8, 2010
Phenotypic expression and origin of the rare beta-thalassemia splice site mutation HBB:c.315 + 1G>TCédrick Broquere, Karine Brudey, Cornelis L Harteveld, et al.
Hemoglobin|June 8, 2010
A new stable alpha chain variant: Hb Basel [alpha14(A12)Trp-->Leu (alpha1)]Martin Hergersberg, Saskia Brunner-Agten, Thomas Kühne, et al.
Hemoglobin|September 22, 2010
Genotype-phenotype relationship of the δ-thalassemia and Hb A(2) variants: observation of 52 genotypesGiuseppina Lacerra, Clelia Scarano, Laura F Lagona, et al.
Hemoglobin|September 22, 2010
New and known β-thalassemia determinants masked by known and new δ gene defects [Hb A(2)-Ramallah or δ6(A3)Glu→Gln, GAG>>CAG]Marion Phylipsen, Cornelis L Harteveld, Menno de Metz, et al.
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