Identification of optimal thalassemia screening strategies for migrant populations in Thailand using a qualitative approach

Autor: Julia Z. Xu, Meghan Foe, Wilaslak Tanongsaksakul, Thidarat Suksangpleng, Supachai Ekwattanakit, Suchada Riolueang, Marilyn J. Telen, Bonnie N. Kaiser, Vip Viprakasit

Publikováno v: BMC Public Health, Vol 21, Iss 1, Pp 1-13 (2021)

Abstract Background Thalassemia is a common inherited hemoglobin disorder in Southeast Asia. Severe thalassemia can lead to significant morbidity for patients and economic strain for under-resourced health systems. Thailand’s thalassemia prevention

Externí odkaz: https://doaj.org/article/7dd87dc605924fb29972b6720a46689b

Association of Xmn I Polymorphism and Hemoglobin E Haplotypes on Postnatal Gamma Globin Gene Expression in Homozygous Hemoglobin E

Autor: Supachai Ekwattanakit, Yuwarat Monteerarat, Suchada Riolueang, Kalaya Tachavanich, Vip Viprakasit

Publikováno v: Advances in Hematology, Vol 2012 (2012)

Background and Objectives. To explore the role of cis-regulatory sequences within the β globin gene cluster at chromosome 11 on human γ globin gene expression related to Hb E allele, we analyze baseline hematological data and Hb F values together w

Externí odkaz: https://doaj.org/article/8b3237e33d224f0b803f3e5dc4e1b8a6

Feasibility of and barriers to thalassemia screening in migrant populations: a cross-sectional study of Myanmar and Cambodian migrants in Thailand

Autor: Suchada Riolueang, Thidarat Suksangpleng, Supachai Ekwattanakit, Julia Z. Xu, Vip Viprakasit, Marilyn J. Telen, Wilaslak Tanongsaksakul

Publikováno v: BMC Public Health
BMC Public Health, Vol 21, Iss 1, Pp 1-15 (2021)

Background Thalassemia, an inherited hemoglobin disorder, has become a global public health problem due to population migration. Evidence-based strategies for thalassemia prevention in migrants are lacking. We characterized barriers to thalassemia sc

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::941a4c1465bfc84ca21f5c6b2ead2287
https://pubmed.ncbi.nlm.nih.gov/34154562

Interaction between Hb E and Hb Yala (HBB:c.129delT); a novel frameshift beta globin gene mutation, resulting in Hemoglobin E/β0 thalassemia

Autor: Supachai Ekwattanakit, Vip Viprakasit, Suchada Riolueang

Publikováno v: Hematology. 23:117-121

OBJECTIVES There are more than 200 known mutations found in patients with β-thalassemia, a possibility to identify an unknown or novel mutation becomes less possible. Here, we report a novel mutation in a patient from Thailand who presented with chr

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6a64e5656ae5933e95e56d8ab8fba937
https://doi.org/10.1080/10245332.2017.1359899

The genetic basis of asymptomatic codon 8 frame-shift (HBB:c25_26delAA) β0-thalassaemia homozygotes

Autor: Sule Unal, Bernard G. Forget, Nejat Akar, Martin H. Steinberg, A. Nazli Basak, Fatma Gumruk, Catherine Badens, Patrick G. Gallagher, Leonor Osorio, Serge Pissard, Nasir A. S. Al-Allawi, Roger Théberge, Andrew D. Campbell, John J. Farrell, Zhihua Jiang, Suchada Riolueang, Philippe Joly, Hong-Yuan Luo, Shengwen Huang, Katherine A. Benson, Vip Viprakasit, Lance Davis, David H.K. Chui

Publikováno v: British Journal of Haematology
British Journal of Haematology, 2016, 172 (6), pp.958-965. ⟨10.1111/bjh.13909⟩
British Journal of Haematology, Wiley, 2016, 172 (6), pp.958-965. ⟨10.1111/bjh.13909⟩

Two 21-year old dizygotic twin men of Iraqi descent were homozygous for HBB codon 8, deletion of two nucleotides (-AA) frame-shift β(0) -thalassaemia mutation (FSC8; HBB:c25_26delAA). Both were clinically well, had splenomegaly, and were never trans

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00e7af49334542d5d63926d0c869ad19
https://doi.org/10.1111/bjh.13909