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Hemoglobin|May 21, 1999
Hb Nijkerk: a new mutation at codons 138/139 of the beta-globin gene inducing severe hemolytic anemia in a Dutch girlH M van den Berg, M C Bruin, D Batelaan, et al.Hemoglobin|May 21, 1999
Characterization and locus assignment of two alpha-globin variants present in the Maltese population: Hb St. Luke's [alpha95(G2)Pro-->Arg] and Hb Setif [alpha94(G1)Asp-->Tyr]S Bezzina Wettinger, R Galdies, C Scerri, et al.Hemoglobin|January 1, 1976
Hemoglobin British Columbia (alpha2beta2 101(G3)Glu replaced by Lys). A new variant with high oxygen affinityR T Jones, B Brimhall, G GrayHemoglobin|June 28, 2000
Diverse genetic mechanisms operate to generate atypical betaS haplotypes in the population of GuadeloupeM Romana, L Kéclard, A Froger, et al.Hemoglobin|February 9, 2018
Newborn Screening for Hemoglobinopathies and Red Cell Enzymopathies in Tripura State: A Malaria-Endemic State in Northeast IndiaDipti Upadhye, Rajat S Das, Jayanta Ray, et al.Hemoglobin|January 10, 2019
A Unique Interaction of IVS-I-1 (G>A) (HBA2: c.95+1G>A) with Hb Adana (HBA2: c.179G>A) Presenting as Transfusion-Dependent α-ThalassemiaHafiza Alauddin, Khairina Kamarudin, Tang Yee Loong, et al.Hemoglobin|January 11, 2019
Successful Outcome of Hyperhemolysis in Sickle Cell Disease following Multiple Lines of Treatment: The Role of Complement InhibitionEfthymia Vlachaki, Eleni Gavriilaki, Katerina Kafantari, et al.Hemoglobin|January 4, 2019
Drepa-Opia: A Pilot Study to Determine the Predictive Factors of Morphine Use and Consumption in Hospitalized Adult Patients with Sickle Cell DiseaseMarie Sabrie, Giovanna Cannas, Karim Tazarourte, et al.Hemoglobin|January 4, 2019
Compound Heterozygosity for Hb D-Ibadan (HBB: c.263C>A) and Hb C (HBB: c.19G>A)Sirisha Kundrapu, Nafiseh Janaki, Howard J MeyersonPageof 238