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Hemoglobin|November 11, 2016
Studies of novel variants associated with Hb F in Sardinians and Tanzanians in sickle cell disease patients from CameroonGift D Pule, Valentina J Ngo Bitoungui, Bernard Chetcha Chemegni, et al.
Hemoglobin|April 26, 2014
Prevalence of low bone mass and vitamin D deficiency in β-thalassemia majorPloutarchos Tzoulis, Ai Leen Ang, Farrukh T Shah, et al.
Hemoglobin|October 1, 2016
Clinical Course of Two Children with Unstable Hemoglobins: The Effect of Hydroxyurea TherapyHarriët M Loovers, Nienke Tamminga, André B Mulder, et al.
Hemoglobin|September 16, 2014
β-Thalassemia mutations in Western India: outcome of prenatal diagnosis in a hemoglobinopathies projectAshwin P Patel, Rupesh B Patel, Saumyaa A Patel, et al.
Hemoglobin|September 16, 2014
Characterization of two unique α-globin gene cluster deletions causing α-thalassemia in Israeli ArabsOded Gilad, Orly Dgany, Sharon Noy-Lotan, et al.
Hemoglobin|October 2, 2014
Blood typing profile of a school-aged population of a North Togo townshipAhoefa Vovor, Lochina Fétéké, Irénée M Kueviakoe, et al.
Hemoglobin|July 31, 2014
Correlation of iron overload and glomerular filtration rate estimated by cystatin C in patients with β-thalassemia majorMurtadha Al-Khabori, Sunil Bhandari, Khalid Al-Rasadi, et al.
Hemoglobin|July 16, 2014
Prevalence of sickle cell disease in a pediatric population suffering from severe infections: a Congolese experienceDiane A Kondani, Jean Lambert Gini-Ehungu, Joseph M Bodi, et al.
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