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Hemoglobin|August 6, 2016
Occurrence of the - -(SEA), - -(THAI) and - -(FIL) α-Thalassemia-1 Carriers from a 7-Year Study at Ramathibodi Hospital, Bangkok, ThailandKobkorn Pongjantharasatien, Wansa Banyatsuppasin, Sonnarong Pounsawat, et al.Hemoglobin|August 6, 2016
Is Vitamin C Supplementation in Patients with β-Thalassemia Major Beneficial or Detrimental?Hadi Darvishi Khezri, Amir Emami Zeydi, Hassan Sharifi, et al.Hemoglobin|January 1, 1989
Cytosine arabinoside plus hemin treatment of a human erythroid cell line, KMOE, strongly induces embryonic, fetal, and adult beta-like globin genesC J Stoeckert, N C Nicolaides, K M HainesHemoglobin|January 1, 1983
Oxygen equilibrium studies of Hb Willamette alpha 2 beta (2)51(D2)Pro leads to ArgM Quarum, T Shih, R T JonesHemoglobin|June 23, 2015
Identification of Two Novel β-Thalassemia Mutations (HBB: c.335-346del and HBB: c.108 C > G) in Han ChineseWenjuan Wang, Qian Wang, Tingting Tao, et al.Hemoglobin|June 27, 2015
A Mixed-Methods Study of Pain-related Quality of Life in Sickle Cell Vaso-Occlusive CrisesRichard J Lin, Arthur T Evans, Kerri Wakeman, et al.Hemoglobin|June 27, 2015
Novel 31.2 kb α0 Deletion in a Palestinian Family with α-ThalassemiaChristian Brieghel, Henrik Birgens, Henrik Frederiksen, et al.Hemoglobin|January 1, 1978
Allosteric effect of o-iodobenzoate on hemoglobinF Taketa, J Y Chen, W F Skogen, et al.Hemoglobin|August 19, 2021
Quality of Life and Related Factors in β-Thalassemia PatientsKoorosh Etemad, Parisa Mohseni, Mohammad Aghighi, et al.Hemoglobin|August 6, 2021
High Systolic Blood Pressure, Anterior Segment Changes and Visual Impairment Independently Predict Sickle Cell RetinopathyIbrahim M Idris, Aminu A Yusuf, Dalha H Gwarzo, et al.Pageof 239