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Hemoglobin|January 1, 1992
Hb City of Hope [beta 69(E13)Gly----Ser] in Italy: association of the gene with haplotype IXM De Angioletti, G Maglione, P Ferranti, et al.Hemoglobin|January 22, 2011
Hb S-β-thalassemia: molecular, hematological and clinical comparisonsGraham R Serjeant, Beryl E Serjeant, Raphael A Fraser, et al.Hemoglobin|January 22, 2011
Fetal hemoglobin response to hydroxyurea in Yemeni sickle cell disease patientsHafiz A Al-Nood, Mona M Al-Khawlani, Ahmed Al-AkwaHemoglobin|November 17, 2010
Bayesian estimates of the prevalence of β-thalassemia trait in voluntary blood donors of central India: a surveyNirupama Chatterjee, Amit Mishra, Ravindra Soni, et al.Hemoglobin|June 8, 2010
The role of iron and chelators on infections in iron overload and non iron loaded conditions: prospects for the design of new antimicrobial therapiesGeorge J Kontoghiorghes, Annita Kolnagou, Anna Skiada, et al.Hemoglobin|June 8, 2010
Iron chelation for amelioration of liver ischemia-reperfusion injuryNikolaos Arkadopoulos, Constantinos Nastos, Konstantinos Kalimeris, et al.Hemoglobin|July 21, 2010
Codon 24 (TAT>TAG) and codon 32 (ATG>AGG) (Hb Rotterdam): two novel alpha2 gene mutations associated with mild alpha-thalassemia found in the same family after newborn screeningPiero C Giordano, Marjon H Cnossen, Annemarie M S Joosten, et al.Hemoglobin|September 22, 2010
Comprehensive spectrum of the β-Thalassemia mutations in Khuzestan, southwest IranHamid Galehdari, Bahaoddin Salehi, Somaiyeh Azmoun, et al.Hemoglobin|September 22, 2010
Further studies on Hb Canebière [β12(G4)Asn→His], a low affinity hemoglobin variantUlf Froelund, Erik Sandbakken, Pal Szecsi, et al.Hemoglobin|September 22, 2010
Hb S-San Martin: a new sickling hemoglobin with two amino acid substitutions [β6(A3)Glu→Val;β105(G7)Leu→Pro] in an Argentinean familyAurora Feliu-Torres, Silvia Eandi Eberle, Irma M Bragós, et al.Pageof 240