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Hemoglobin|April 1, 2017
Hb Alesha [β67(E11)Val→Met (GTG>ATG); HBB: c.202G > A] Found in a Chinese GirlHua Jiang, Jin-Mei Yan, Jian-Ying Zhou, et al.Hemoglobin|April 1, 2017
Genetic Variants at BCL11A and HBS1L-MYB loci Influence Hb F Levels in Chinese Zhuang β-Thalassemia Intermedia PatientsYunli Lai, Yun Chen, Biyan Chen, et al.Hemoglobin|April 4, 2017
Mutational Profile of Homozygous β-Thalassemia in Rio de Janeiro, BrazilGisele C S Carrocini, Larissa P R Venancio, Viviani L R Pessoa, et al.Hemoglobin|April 5, 2017
Insulin Secretion and Resistance in Normoglycemic Patients with Sickle Cell DiseaseMaria P Yavropoulou, Maria Pikilidou, Despoina Pantelidou, et al.Hemoglobin|January 30, 2014
A new δ chain variant, Hb A2-Tunis [δ46(CD5)Gly → Glu; HBD: c.140G>A], observed in a Tunisian family in association with a compound heterozygosity for Hb C [β6(A3)Glu → Lys; HBB: c.19G>A] β(0)-thalassemia [IVS-I-1 (β143, G>A); HBB: c.92+1G>A]Imen Moumni, Amine Zorai, Sonia Mahjoub, et al.Hemoglobin|January 30, 2014
Two new hemoglobin variants: Hb Tallahassee [α3(A1)Ser→Tyr; HBA2: c.11C>A] and Hb madison-NC [β119(GH2)Gly→Ser; HBB: c.358G>A]Ferdane Kutlar, Yoram Unguru, Natalia Dixon, et al.Hemoglobin|April 12, 2017
Hb Presbyterian (HBB: c.327C>G) in a Nicaraguan FamilyAllan Pernudy-Ubau, Jaslyn Salinas-Molina, Yaneris Requenez, et al.Hemoglobin|March 28, 2014
Challenge of managing sickle cell disease in a pediatric population living in kinshasa, democratic republic of congo: a sickle cell center experienceMichel Ntetani Aloni, Leonard NkeeHemoglobin|March 28, 2014
Proteasome inhibition induces both antioxidant and hb f responses in sickle cell disease via the nrf2 pathwayVinod Pullarkat, Zhuo Meng, Stanley M Tahara, et al.Hemoglobin|January 1, 1988
Overview of the beta thalassemias: genetic and clinical aspectsE Schwartz, A Cohen, S SurreyPageof 240