High resolution melting analysis: a rapid screening and typing tool for common β-thalassemia mutation in Chinese population

M Lin, JW Jiao, XH Zhan, XF Zhan, MC Pan, JL Wang… - PLoS …, 2014 - journals.plos.org
β-thalassemia is a common inherited disorder worldwide including southern China, and at
least 45 distinct β-thalassemia mutations have been identified in China. High-resolution …

Prevalence of α-thalassaemia genotypes in pregnant women in northern Thailand

S Pharephan, P Sirivatanapa… - Indian Journal of …, 2016 - journals.lww.com
Methods: Genomic DNA was extracted from blood samples of pregnant women who came to
Maharaj Nakorn Chiang Mai University Hospital during July 2009 to 2010. The common …

The prevalence of alpha-thalassemia amongst Tai and Mon-Khmer ethnic groups residing in northern Thailand: A population-based study

P Lithanatudom, P Khampan, DR Smith, S Svasti… - …, 2016 - Taylor & Francis
Background: Northern Thailand is one of the highest α-thalassemia incidence areas where
30–40% of inhabitants have been reported to carry aberrant α-globin genes. However, all …

[PDF][PDF] Hemoglobin Q-Thailand and its combinations with other forms of thalassemia or hemoglobinopathies in northern Thailand

S Panyasai, S Pornprasert - Clin Lab, 2014 - researchgate.net
Background: There have been no reports for the frequency of Hb Q-Thailand [α 74 (EF3)
Asp→ His, GAC> CAC] and its combinations either with other forms of thalassemia or …

Hb Dartmouth (HBA2: c.200T>C): An α2-Globin Gene Associated with Hb H Disease in One Homozygous Patient

S Farashi, N Faramarzi Garous, M Ashki, S Vakili… - …, 2015 - Taylor & Francis
Hb H (β4) disease is caused by deletion or inactivation of three out of four α-globin genes. A
high incidence of Hb H disease has been reported all over the world. There is a wide …

Epidemiology of hemoglobinopathies in the huzhou region, zhejiang province, southeast China

ZY Ding, GS Shen, S Zhang, PY He - Hemoglobin, 2016 - Taylor & Francis
The aim of the present study was to report the frequency of thalassemia traits and other
hemoglobinopathies in Huzhou City, Zhejiang Province, People's Republic of China (PRC) …

Detection of coinherited Hb H-Constant Spring/Paksé disease and Hb E by capillary electrophoresis and high performance liquid chromatography

S Pornprasert, J Waneesorn - Hemoglobin, 2013 - Taylor & Francis
A capillary electrophoresis (CE) method has been proven to be superior to a high
performance liquid chromatography (HPLC) method in the detection of Hb H-Constant …

Detection of Hb Constant Spring (HBA2: c.427T>C) Heterozygotes in Combination with β-Thalassemia or Hb E Trait by Capillary Electrophoresis

S Pornprasert, S Saoboontan, M Punyamung - Hemoglobin, 2015 - Taylor & Francis
Abstract Hb Constant Spring (Hb CS; HBA2: c. 427T> C) is often missed by routine
laboratory testing as its mRNA as well as gene product are unstable and presented at a low …

Iron deficiency anemia interfering the diagnosis of compound heterozygosity for Hb constant spring and Hb Paksé: The first case report

T Chiasakul, N Uaprasert - Journal of Clinical Laboratory …, 2018 - Wiley Online Library
Background Diagnosis of thalassemia or hemoglobinopathy concomitant with iron
deficiency anemia (IDA) is challenging. Method We report a case of 43‐year‐old female …

[PDF][PDF] NGHI£ N CøU § ÆC § IÓM L¢ M SµNG, KIÓU GEN CñA BÖNH HBH Vµ CHÈN § ON TR¦ íC SINH BÖNH α THALASSEMIA

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