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Hemoglobin|May 6, 2026
Beyond Diagnosis: A Systematic Review of Artificial Intelligence and Deep Learning in Monitoring Iron Overload and Organ Toxicity in Beta-ThalassemiaAbdulrahman Nasiri, Mostafa F Mohammed Saleh, Manal Alshammari, et al.Hemoglobin|May 13, 2026
Prenatal Counseling Conundrum: Unexpectedly Mild Phenotype in a Pregnant Woman with Homozygous CD41/42(-TTCT) β-ThalassemiaJing Guo, Teng Li, Liang Liang, et al.Hemoglobin|June 9, 2026
Genotypic Characterization of Hemoglobinopathies in Azerbaijan: A Review of 10 Years at a Referral CenterAgharza Aghayev, Khuraman Jafarova, Zenfira Mirzeyeva, et al.Hemoglobin|June 9, 2026
Pyruvate Kinase Activation in the Management of Thalassemia and Sickle Cell DiseaseKhaled M Musallam, Biree AndemariamHemoglobin|October 26, 2012
Two assays to evaluate potential genotoxic effects of hydroxyurea in sickle cell disease patientsAnar Rodríguez, Leonard Kouegnigan, Alina Ferster, et al.Hemoglobin|November 5, 2020
Detection of an α-Globin Fusion Gene Using Real-Time Polymerase Chain Reaction-Based Multicolor Melting CurveAi-Ping Ju, Fan Jiang, Jian Li, et al.Hemoglobin|January 1, 1985
Hb Aztec or alpha 2 76 (EF5) Met----Thr beta 2 detection of a silent mutant by high performance liquid chromatographyJ B Shelton, J R Shelton, W A Schroeder, et al.Hemoglobin|February 1, 2019
Quality of Life of Pakistani Children with β-Thalassemia MajorHumaira Yasmeen, Shahida HasnainHemoglobin|July 27, 2007
Hb Zoetermeer: a new mutation on the alpha2 gene inducing an Ala-->Ser substitution at codon 21 is possibly associated with a mild thalassemic phenotypeCornelis L Harteveld, Willem C H van Helden, George L Boxma, et al.Hemoglobin|January 1, 1979
Complete sequence of the gamma chain from the fetal hemoglobin of the baboon, Papio cynocephalusP E Nute, W C MahoneyPageof 240