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Hemoglobin|July 16, 2014
The effect and side effect of hydroxyurea therapy on patients with β-thalassemia: a systematic review to December 2012Mehrnoush Kosaryan, Mandana Zafari, Abbass Alipur, et al.Hemoglobin|April 26, 2013
Interaction of Hb adana (HBA2: c.179G>A) with deletional and nondeletional α(+)-thalassemia mutations: diverse hematological and clinical featuresIta M Nainggolan, Alida Harahap, Debby D Ambarwati, et al.Hemoglobin|April 19, 2013
The current status of β-thalassemia major in Mainland ChinaLu-Hong Xu, Jian-Pei FangHemoglobin|April 23, 2013
Leg ulcers in sickle cell disease: current patterns and practicesKara-Marie H Delaney, Karen C Axelrod, Ashley Buscetta, et al.Hemoglobin|April 23, 2013
A new β(0)-thalassemia mutation (codon 102, AAC>ATCAC) in coexistence with a heterozygous P4.2 Nippon geneChris Adhiyanto, Yasuhiro Yamashiro, Yukio Hattori, et al.Hemoglobin|May 9, 2013
Mild β(+)-thalassemia associated with two linked sequence variants: IVS-II-839 (T>C) and IVS-II-844 (C>A)John S Waye, Barry Eng, Laurie Hellens, et al.Hemoglobin|February 22, 2013
Prevalence and molecular characterization of β-thalassemia in the state of Bahia, Brazil: first identification of mutation HBB: c.135delC in BrazilSilvana F Fonseca, Jose P Moura Neto, Marilda S GoncalvesHemoglobin|March 9, 2013
Secular trends in the national and provincial births of new thalassemia cases in Iran from 2001 to 2006Mahmoud Hadipour Dehshal, Alireza Ahmadvand, Sakineh Yousefi Darestani, et al.Hemoglobin|January 30, 2013
Microdeletion of exon 3 in the HBA2 gene associated with mild α-thalassemia traitAnne Lambert, Ann Y K Wong, Yohji Kominami, et al.Pageof 240