Citations (28)
Keep up to date with the latest research on this topic with citation updates for this article.
Read on this site (12)
Rossarin Karnpean, Amarin Narkwichean, Wipada Laosooksathit, Prapaporn Panichchob & Wittaya Jomoui. (2023) Direct cord blood LAMP colorimetric phenol red assay for detecting α0-thalassemia (SEA deletion); the validation and post-natal screening in Thailand. Scandinavian Journal of Clinical and Laboratory Investigation 83:7, pages 495-500.
Read now
Read now
Mina Ebrahimi, Javad Mohammadi-Asl & Fakher Rahim. (2021) The worldwide molecular spectrum and distribution of thalassaemia: a systematic review. Annals of Human Biology 48:4, pages 307-312.
Read now
Read now
Prapaporn Panichchob, Pooncharus Iamdeelert, Putita Wongsariya, Pitchaya Wongsariya, Pinnaree Wongwattanasanti, Wanicha Tepakhan & Wittaya Jomoui. (2021) Molecular Spectrum of β-Thalassemia Mutations in Central to Eastern Thailand. Hemoglobin 45:2, pages 97-102.
Read now
Read now
Sitthichai Panyasai, Naowarat Kunyanone & Surada Satthakarn. (2021) Hb Athens-Georgia (beta 40(C6) Arg > Lys, HBB:c.122G > A) with a single α-globin gene (Hb H disease) in a Thai family: molecular, hematological, and diagnostic aspects. Scandinavian Journal of Clinical and Laboratory Investigation 81:1, pages 52-58.
Read now
Read now
Amna Tariq, Sana Khurshid & Muhammad Sajjad. (2021) Evaluation of the High Resolution Melting Approach for Detection of β-Thalassemia Gene Mutations. Hemoglobin 45:1, pages 20-24.
Read now
Read now
Chanchai Traivaree, Chalinee Monsereenusorn, Piya Rujkijyanont, Warakorn Prasertsin & Boonchai Boonyawat. (2018) Genotype–phenotype correlation among beta-thalassemia and beta-thalassemia/HbE disease in Thai children: predictable clinical spectrum using genotypic analysis. Journal of Blood Medicine 9, pages 35-41.
Read now
Read now
Yuan Zhao, Lv-Yin Huang, Fan Jiang, Jian-Ying Zhou, Xing-Mei Xie & Dong-Zhi Li. (2017) Hb Hornchurch [β43(CD2)Glu→Lys; HBB: c.130G>A] Compromises the Molecular Diagnosis of β-Thalassemia in a Chinese Family. Hemoglobin 41:4-6, pages 274-277.
Read now
Read now
Boonchai Boonyawat, Chalinee Monsereenusorn & Chanchai Traivaree. (2014) Molecular analysis of beta-globin gene mutations among Thai beta-thalassemia children: results from a single center study. The Application of Clinical Genetics 7, pages 253-258.
Read now
Read now
Pimlak Charoenkwan, Pimjan Teerachaimahit & Torpong Sanguansermsri. (2014) The Correlation of α-Globin Gene Mutations and the XmnI Polymorphism with Clinical Severity of Hb E/β-Thalassemia. Hemoglobin 38:5, pages 335-338.
Read now
Read now
Supatra Sirichotiyakul, Rattika Saetung & Torpong Sanguansermsri. (2009) Prenatal Diagnosis of β-Thalassemia/Hb E by Hemoglobin Typing Compared to DNA Analysis. Hemoglobin 33:1, pages 17-23.
Read now
Read now
Saisiri Mirasena, Dawan Shimbhu, Mondhon Sanguansermsri & Torpong Sanguansermsri. (2008) Detection of β-Thalassemia Mutations Using a Multiplex Amplification Refractory Mutation System Assay. Hemoglobin 32:4, pages 403-409.
Read now
Read now
Gebhard Flatz, Torpong Sanguansermsri, Sourideth Sengchanh, David Horst & Jürgen Horst. (2004) The ‘Hot Spot’ of Hb E [β26(B8)Glu→Lys] in Southeast Asia: β‐Globin Anomalies in the Lao Theung Population of Southern Laos. Hemoglobin 28:3, pages 197-204.
Read now
Read now
Articles from other publishers (16)
Surada Satthakarn, Kesorn Panyasai, Amphai Phasit & Sitthichai Panyasai. (2023)
Reliability of hemoglobin A
2
value as measured by the Premier Resolution system for screening of β-thalassemia carriers
. Clinical Chemistry and Laboratory Medicine (CCLM) 0:0.
Crossref
Crossref
Avani Shah, Sumit Bharadva, Parizad Patel & Kanchan Mishra. 2022. Hepatitis B. Hepatitis B.
Wanicha Tepakhan & Wittaya Jomoui. (2021) Rapid molecular diagnostics of large deletional β0-thalassemia (3.5 kb and 45 kb) using colorimetric LAMP in various thalassemia genotypes. Heliyon 7:11, pages e08372.
Crossref
Crossref
Phongsathorn Wichian, Supawadee Yamsri, Kanokwan Sanchaisuriya & Supan Fucharoen. (2021) Direct Amplification of Whole Blood and Amniotic Fluid Specimens for Prenatal and Postnatal Diagnosis of Hb E-β 0-Thalassemia Diseases. Laboratory Medicine 52:5, pages 460-468.
Crossref
Crossref
Chane Choed-Amphai, Arunee Phusua, Chupong Ittiwut, Pimlak Charoenkwan, Kanya Suphapeetiporn & Vorasuk Shotelersuk. (2021) Coinherited Hemoglobin H/Constant Spring Disease and Heterozygous Hemoglobin Tak Causing Severe Hemolytic Anemia in a Thai Boy. Journal of Pediatric Hematology/Oncology 43:5, pages e723-e726.
Crossref
Crossref
Thongperm Munkongdee, Ping Chen, Pranee Winichagoon, Suthat Fucharoen & Kittiphong Paiboonsukwong. (2020) Update in Laboratory Diagnosis of Thalassemia. Frontiers in Molecular Biosciences 7.
Crossref
Crossref
Adivitch Sripusanapan, Arunee Phusua, Kanda Fanhchaksai & Pimlak Charoenkwan. (2020)
Compound heterozygosity of a silent beta‐thalassemia mutation at the 3′‐untranslated region (
HBB
: c.*132 C>T) and beta‐zero thalassemia results in thalassemia intermedia
. Pediatric Blood & Cancer 67:4.
Crossref
Crossref
Kanittha Mankhemthong, Arunee Phusua, Sudjai Suanta, Pitipong Srisittipoj, Pimlak Charoenkwan & Torpong Sanguansermsri. (2019) Molecular characteristics of thalassemia and hemoglobin variants in prenatal diagnosis program in northern Thailand. International Journal of Hematology 110:4, pages 474-481.
Crossref
Crossref
Phumin Chaweephisal, Arunee Phusua, Kanda Fanhchaksai, Supatra Sirichotiyakul & Pimlak Charoenkwan. (2019) Borderline hemoglobin A2 levels in northern Thai population: HBB genotypes and effects of coinherited alpha-thalassemia. Blood Cells, Molecules, and Diseases 74, pages 13-17.
Crossref
Crossref
Pimlak Charoenkwan, Supatra Sirichotiyakul, Arunee Phusua, Sudjai Suanta, Kanda Fanhchaksai, Rattika Sae-Tung & Torpong Sanguansermsri. (2017) High-resolution melting analysis for prenatal diagnosis of beta-thalassemia in northern Thailand. International Journal of Hematology 106:6, pages 757-764.
Crossref
Crossref
Peerapon Wong, Arunee Srichaiya, Pawanrat Suannum, Prissana Charoenporn, Sawichayaporn Jermnim, Monthira Chan-In, Akamon Tapprom & Rawisut Deoisares. (2017) Frequency of hemoglobin E/β-thalassemia compound heterozygotes with low hemoglobin F phenotype among cases with a diagnosis of hemoglobin E homozygote, determined by high-performance liquid chromatography, in prenatal control program for β-thalassemia. Annals of Hematology 96:10, pages 1763-1765.
Crossref
Crossref
Supawadee Yamsri, Kanokwan Sanchaisuriya, Goonnapa Fucharoen, Nattaya Sae-ung & Supan Fucharoen. (2011) Genotype and phenotype characterizations in a large cohort of β-thalassemia heterozygote with different forms of α-thalassemia in northeast Thailand. Blood Cells, Molecules, and Diseases 47:2, pages 120-124.
Crossref
Crossref
Pimlak Charoenkwan, Rawee Taweephol, Supatra Sirichotiyakul, Watcharee Tantiprabha, Rattika Sae-Tung, Sudjai Suanta, Pimonrat Sakdasirisathaporn & Torpong Sanguansermsri. (2010) Cord blood screening for α-thalassemia and hemoglobin variants by isoelectric focusing in northern Thai neonates: Correlation with genotypes and hematologic parameters. Blood Cells, Molecules, and Diseases 45:1, pages 53-57.
Crossref
Crossref
Owen T. M. Chan, Kenneth D. Westover, Lisa Dietz, James L. Zehnder & Iris Schrijver. (2010)
Comprehensive and Efficient
HBB
Mutation Analysis for Detection of β-Hemoglobinopathies in a Pan-Ethnic Population
. American Journal of Clinical Pathology 133:5, pages 700-707.
Crossref
Crossref
S. K. SANGKITPORN, L. EKSIRI, A. SANGNOI, S. DUANGRUANG, A. DUMBUA, K. RATTANAKITTISOPHON & S. SANGKITPORN. (2009) Identification of β-globin gene mutations in Thailand using an automated fluorescence-based DNA sequencer. International Journal of Laboratory Hematology 31:5, pages 521-527.
Crossref
Crossref
Nelly Briand, Sakorn Pornprasert, Nicole Ngo-Giang-Huong, Fréderic Galactéros, Serge Pissard, Thanusak Tatu, Torpong Sanguansermsri, Gonzague Jourdain, Marc Lallemant & Sophie Le Coeur. (2009) Perinatal zidovudine prophylaxis in HIV type-1-infected pregnant women with thalassaemia carriage in Thailand. Antiviral Therapy 14:1, pages 117-122.
Crossref
Crossref