Citations (49)
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Phongsathorn Wichian, Supawadee Yamsri, Attawut Chaibunruang, Cholthicha KerdKaew, Dhanawan Thongsee, Hataichanok Srivorakun & Supan Fucharoen. (2021) Direct PCR assays without DNA extraction for rapid detection of hemoglobin Constant Spring and Pakse' genes: application for carrier screening and prenatal diagnosis. Scandinavian Journal of Clinical and Laboratory Investigation 81:7, pages 557-563.
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Roongnalin Bunthupanich, Rossarin Karnpean, Anuwat Pinyachat, Nawinda Jiambunsri, Nattapol Prakobkaew, Naruwat Pakdee, Supan Fucharoen & Suthat Fucharoen. (2020) Micromapping of Thalassemia and Hemoglobinopathies Among Laos, Khmer, Suay and Yer Ethnic Groups Residing in Lower Northeastern Thailand. Hemoglobin 44:3, pages 162-167.
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Samaneh Farashi, Negin Faramarzi Garous, Mehri Ashki, Shadi Vakili, Fatemah Zeinali, Hashem Imanian, Azita Azarkeivan & Hossein Najmabadi. (2015) Hb Dartmouth (HBA2: c.200T>C): An α2-Globin Gene Associated with Hb H Disease in One Homozygous Patient. Hemoglobin 39:3, pages 152-155.
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Raewadee Wisedpanichkij, Sumalee Jindadamrongwech & Punnee Butthep. (2015) Identification of Hb Constant Spring (HBA2: c.427T > C) by an Automated High Performance Liquid Chromatography Method. Hemoglobin 39:3, pages 190-195.
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Hoa Van Nguyen, Kanokwan Sanchaisuriya, Dung Nguyen, Hoa Thi Thuy Phan, Sirivara Siridamrongvattana, Pattara Sanchaisuriya, Supan Fucharoen, Goonnapa Fucharoen & Frank P. Schelp. (2013) Thalassemia and Hemoglobinopathies in Thua Thien Hue Province, Central Vietnam. Hemoglobin 37:4, pages 333-342.
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Sakorn Pornprasert & Jarurin Waneesorn. (2013) Detection of Coinherited Hb H-Constant Spring/Paksé Disease and Hb E by Capillary Electrophoresis and High Performance Liquid Chromatography. Hemoglobin 37:2, pages 176-182.
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Kritsada Singha, Hataichanok Srivorakun, Goonnapa Fucharoen, Yossombat Changtrakul, Patcharee Komwilaisak, Arunee Jetsrisuparb, Rawiwan Puangplruk & Supan Fucharoen. (2013) Association of Hb Thailand [α56(E5)Lys→Thr] and Hb Phnom Penh [α117(GH5)-Ile-α118(H1)] with α0-Thalassemia: Molecular and Hematological Features and Differential Diagnosis. Hemoglobin 37:1, pages 37-47.
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Sakorn Pornprasert, Sitthichai Panyasai & Kallayanee Treesuwan. (2012) Unmasking Hb Paksé (codon 142, TAA>TAT, α2) and its Combinations in Patients also Carrying Hb Constant Spring (codon 142, TAA>CAA, α2) in Northern Thailand. Hemoglobin 36:5, pages 491-496.
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Jaruwan Tritipsombut, Kanokwan Sanchaisuriya, Prachatip Phollarp, Dalouny Bouakhasith, Pattara Sanchaisuriya, Goonnapa Fucharoen, Supan Fucharoen & Frank P. Schelp. (2012) Micromapping of Thalassemia and Hemoglobinopathies in Diferent Regions of Northeast Thailand and Vientaine, Laos People's Democratic Republic. Hemoglobin 36:1, pages 47-56.
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Sanita Singsanan, Hataichanok Srivorakun, Goonnapa Fucharoen, Rawiwan Puangplruk & Supan Fucharoen. (2011) Hb Phimai [β72(E16)Ser→Thr]: A Novel β-Globin Structural Variant Found in Association with Hb Constant Spring in Pregnancy. Hemoglobin 35:2, pages 103-110.
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Viroj Wiwanitkit. (2006) Tertiary structural analysis of the elongated part of an abnormal hemoglobin, hemoglobin Pakse. International Journal of Nanomedicine 1:1, pages 105-107.
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Pimlak Charoenkwan, Rawee Taweephon, Rattika Sae-Tung, Pattra Thanarattanakorn & Torpong Sanguansermsri. (2005) Molecular and Clinical Features of Hb H Disease in Northern Thailand. Hemoglobin 29:2, pages 133-140.
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Supan Fucharoen, Sunisa Chunpanich, Kanokwan Sanchaisuriya, Goonnapa Fucharoen & Naowarat Kunyanone. (2005) Thalassemia Intermedia Associated with Complex Interaction of Hb Beijing [α16(A14)Lys→Asn] and Hb E [β26(B8)Glu→Lys] with a Deletional α-Thalassemia-1 in a Thai Family. Hemoglobin 29:1, pages 77-83.
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Vip Viprakasit, Worrawut Chinchang, Waraporn Glomglao & Voravarn S Tanphaichitr. (2005) A Rare Association of α0-Thalassemia (– –SEA) and an Initiation Codon Mutation (ATG→A-G) of the α2 Gene Causes Hb H Disease in Thailand. Hemoglobin 29:3, pages 235-240.
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Articles from other publishers (35)
Rossarin Karnpean, Nawinda Vanichakulthada, Wanwisa Suwannaloet, Ruttiya Thongrung, Sanita Singsanan, Nattapol Prakobkaew, Goonnapa Fucharoen & Supan Fucharoen. (2022) Anemia, iron deficiency, and thalassemia among the Thai population inhabiting at the Thailand-Lao PDR-Cambodia triangle. Scientific Reports 12:1.
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Jutatip Jamnok, Kanokwan Sanchaisuriya, Pattara Sanchaisuriya, Goonnapa Fucharoen, Supan Fucharoen & Faruk Ahmed. (2020) Factors associated with anaemia and iron deficiency among women of reproductive age in Northeast Thailand: a cross-sectional study. BMC Public Health 20:1.
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Jutatip Jamnok, Kanokwan Sanchaisuriya, Chaninthorn Chaitriphop, Pattara Sanchaisuriya, Goonnapa Fucharoen & Supan Fucharoen. (2020) A New Indicator Derived From Reticulocyte Hemoglobin Content for Screening Iron Deficiency in an Area Prevalent for Thalassemia. Laboratory Medicine 51:5, pages 498-506.
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Benchawan Kingchaiyaphum, Kanokwan Sanchaisuriya, Goonnapa Fucharoen, Attawut Chaibunruang, Sonja Y. Hess, Guy‐Marino Hinnouho, Maxwell A. Barffour, Kimbery R. Wessells, Sengchanh Kounnavong & Supan Fucharoen. (2020)
Hemoglobins F, A
2
, and E levels in Laotian children aged 6‐23 months with Hb E disorders: Effect of age, sex, and thalassemia types
. International Journal of Laboratory Hematology 42:3, pages 277-283.
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Mostafa Paridar, Ebrahim Azizi, Bijan Keikhaei, Vahideh Takhviji, Iman Baluchi & Abbas Khosravi. (2019) Iranian patients with hemoglobin H disease: genotype–phenotype correlation. Molecular Biology Reports 46:5, pages 5041-5048.
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Kritsada Singha, Wachiraporn Taweenan, Goonnapa Fucharoen & Supan Fucharoen. (2019) Erythrocyte indices in a large cohort of β‐thalassemia carrier: Implication for population screening in an area with high prevalence and heterogeneity of thalassemia. International Journal of Laboratory Hematology.
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Thita Chiasakul & Noppacharn Uaprasert. (2018) Iron deficiency anemia interfering the diagnosis of compound heterozygosity for Hb constant spring and Hb Paksé: The first case report. Journal of Clinical Laboratory Analysis 32:1, pages e22187.
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Nga Thi Nguyen, Kanokwan Sanchaisuriya, Pattara Sanchaisuriya, Hoa Van Nguyen, Hoa Thi Thuy Phan, Goonnapa Fucharoen & Supan Fucharoen. (2017) Thalassemia and hemoglobinopathies in an ethnic minority group in Central Vietnam: implications to health burden and relationship between two ethnic minority groups. Journal of Community Genetics 8:3, pages 221-228.
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Orathai Tangvarasittichai, Nares Poonanan & Surapon Tangvarasittichai. (2016) Using Red Cell Indices and Reticulocyte Parameters for Carrier Screening of Various Thalassemia Syndromes. Indian Journal of Clinical Biochemistry 32:1, pages 61-67.
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V. Viprakasit. (2015) α−thalassaemia: a genotype-phenotype correlation and management. ISBT Science Series 10:S1, pages 295-304.
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Van Hoa Nguyen, Kanokwan Sanchaisuriya, Kasama Wongprachum, Mau Duyen Nguyen, Thi Thuy Hoa Phan, Van Thang Vo, Pattara Sanchaisuriya, Supan Fucharoen & Frank P. Schelp. (2014) Hemoglobin Constant Spring is markedly high in women of an ethnic minority group in Vietnam: A community-based survey and hematologic features. Blood Cells, Molecules, and Diseases 52:4, pages 161-165.
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Attawut Chaibunruang, Rossarin Karnpean, Goonnapa Fucharoen & Supan Fucharoen. (2014) Genetic heterogeneity of hemoglobin AEBart's disease: A large cohort data from a single referral center in northeast Thailand. Blood Cells, Molecules, and Diseases 52:4, pages 176-180.
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Kritsada Singha, Goonnapa Fucharoen, Arunee Jetsrisuparb & Supan Fucharoen. (2013) Molecular and hematological characteristics of a novel form of α-globin gene triplication: The hemoglobin St.Luke's-Thailand [α95(G2)Pro→Arg] or Hb St. Luke's [A2] HBA2. Clinical Biochemistry 46:7-8, pages 675-680.
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Sirivara Siridamrongvattana, Nguyen Van Hoa, Kanokwan Sanchaisuriya, Nguyen Dung, Phan Thi Thuy Hoa, Pattara Sanchaisuriya, Goonnapa Fucharoen, Supan Fucharoen & Frank P. Schelp. (2013) Burden of Anemia in Relation to Thalassemia and Iron Deficiency among Vietnamese Pregnant Women. Acta Haematologica 130:4, pages 281-287.
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G. FUCHAROEN, H. SRIVORAKUN, S. SINGSANAN & S. FUCHAROEN. (2011) Presumptive diagnosis of common haemoglobinopathies in Southeast Asia using a capillary electrophoresis system. International Journal of Laboratory Hematology 33:4, pages 424-433.
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Hataichanok Srivorakun, Goonnapa Fucharoen, Rawiwan Puangplruk, Napat Kheawon & Supan Fucharoen. (2011) Complex interaction of hemoglobin (Hb) Nakhon Ratchasima [α63(E12)Ala→Val], a novel α2-globin chain variant with Hb E [β26(B8)Glu→Lys] and a deletional α+-thalassemia. European Journal of Haematology 87:1, pages 68-72.
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Nichathorn Panomai, Kanokwan Sanchaisuriya, Supawadee Yamsri, Pattara Sanchaisuriya, Goonnapa Fucharoen, Supan Fucharoen & Frank P. Schelp. (2010) Thalassemia and iron deficiency in a group of northeast Thai school children: relationship to the occurrence of anemia. European Journal of Pediatrics 169:11, pages 1317-1322.
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Vichai Laosombat, Vip Viprakasit, Thirachit Chotsampancharoen, Malai Wongchanchailert, Sudarat Khodchawan, Worawut Chinchang & Benjamas Sattayasevana. (2009) Clinical features and molecular analysis in Thai patients with HbH disease. Annals of Hematology 88:12, pages 1185-1192.
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Jaruwan Tritipsombut, Kanokwan Sanchaisuriya, Supan Fucharoen, Goonnapa Fucharoen, Nirut Siriratmanawong, Charnchai Pinmuang-ngam & Pattara Sanchaisuriya. (2008) Hemoglobin Profiles and Hematologic Features of Thalassemic Newborns: Application to Screening of α-Thalassemia 1 and Hemoglobin E. Archives of Pathology & Laboratory Medicine 132:11, pages 1739-1745.
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Kanokwan Sanchaisuriya, Sunisa Chirakul, Hataichanok Srivorakun, Goonnapa Fucharoen, Supan Fucharoen, Yossombat Changtrakul & Pattara Sanchaisuriya. (2008) Effective screening for double heterozygosity of Hb E/α0-thalassemia. Annals of Hematology 87:11, pages 911-914.
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Chulaporn Chaisue, Suttiphan Kitcharoen, Prapon Wilairat, Arunee Jetsrisuparb, Goonnapa Fucharoen & Supan Fucharoen. (2007) α/β-Globin mRNA ratio determination by multiplex quantitative real-time reverse transcription-polymerase chain reaction as an indicator of globin gene function. Clinical Biochemistry 40:18, pages 1373-1377.
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Sanita Singsanan, Goonnapa Fucharoen, Onekham Savongsy, Kanokwan Sanchaisuriya & Supan Fucharoen. (2007) Molecular characterization and origins of Hb Constant Spring and Hb Paksé in Southeast Asian populations. Annals of Hematology 86:9, pages 665-669.
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Thanyachai Sura, Objoon Trachoo, Vip Viprakasit, Prin Vathesatogkit, Atchara Tunteeratum, Manisa Busabaratana, Raewadee Wisedpanichkij & Parttraporn Isarangkura. (2007) Hemoglobin H disease induced by the common SEA deletion and the rare hemoglobin Quong Sze in a Thai female: longitudinal clinical course, molecular characterization, and development of a PCR/RFLP-based detection method. Annals of Hematology 86:9, pages 659-663.
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Kanokwan Sanchaisuriya, Supan Fucharoen, Thawalwong Ratanasiri, Pattara Sanchaisuriya, Goonnapa Fucharoen, Ekkehart Dietz & Frank P Schelp. (2007) Effect of the maternal βE-globin gene on hematologic responses to iron supplementation during pregnancy. The American Journal of Clinical Nutrition 85:2, pages 474-479.
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Kanokwan Sanchaisuriya, Supan Fucharoen, Thawalwong Ratanasiri, Pattara Sanchaisuriya, Goonnapa Fucharoen, Ekkahart Dietz & Frank P. Schelp. (2006) Thalassemia and hemoglobinopathies rather than iron deficiency are major causes of pregnancy-related anemia in northeast Thailand. Blood Cells, Molecules, and Diseases 37:1, pages 8-11.
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Goonnapa Fucharoen, Jaruwan Trithipsombat, Suparerk Sirithawee, Supawadee Yamsri, Yossombat Changtrakul, Kanokwan Sanchaisuriya & Supan Fucharoen. (2006) Molecular and hematological profiles of hemoglobin EE disease with different forms of α-thalassemia. Annals of Hematology 85:7, pages 450-454.
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Arunee Jetsrisuparb, Kanokwan Sanchaisuriya, Goonnapa Fucharoen, Supan Fucharoen, Surapon Wiangnon, Charoon Jetsrisuparb, Jittima Sirijirachai & Kanchana Chansoong. (2006) Development of Severe Anemia During Fever Episodes in Patients With Hemoglobin E Trait and Hemoglobin H Disease Combinations. Journal of Pediatric Hematology/Oncology 28:4, pages 249-253.
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Pranee Sutcharitchan, Wen Wang, Rung Settapiboon, Supaporn Amornsiriwat, Arnold SC TanSamuel S Chong–. (2005) Hemoglobin H Disease Classification by Isoelectric Focusing: Molecular Verification of 110 Cases from Thailand. Clinical Chemistry 51:3, pages 641-644.
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Kanokwan Sanchaisuriya, Sunisa Chunpanich, Supan Fucharoen, Goonnapa Fucharoen, Pattara Sanchaisuriya & Yossombat Changtrakun. (2005) Association of Hb Q-Thailand with homozygous Hb E and heterozygous Hb Constant Spring in pregnancy. European Journal of Haematology 74:3, pages 221-227.
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Kanokwan Sanchaisuriya, Supan Fucharoen, Goonnapa Fucharoen, Thawalwong Ratanasiri, Pattara Sanchaisuriya, Yossombat Changtrakul, Uthai Ukosanakarn, Wichai Ussawaphark & Frank P. Schelp. (2005) A Reliable Screening Protocol for Thalassemia and Hemoglobinopathies in Pregnancy. American Journal of Clinical Pathology 123:1, pages 113-118.
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S. Chunpanich, K. Ayukarn, K. Sanchaisuriya, G. Fucharoen & S. Fucharoen. (2004) Laboratory diagnosis of a compound heterozygosity for Hb Hekinan [alpha27(B8) Glu-Asp] and a deletional alpha-thalassaemia 2 in Thailand. Clinical and Laboratory Haematology 26:5, pages 355-358.
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Chairat Turbpaiboon, Atchasai Siritantikorn, Wanna Thongnoppakhun, Duangkamon Bunditworapoom, Chanin Limwongse, Pa-thai Yenchitsomanus, Noppadol Siritanaratkul & Prapon Wilairat. (2004) Hemoglobin Pakse: Presence on Red Blood Cell Membrane and Detection by Polymerase Chain Reaction-Single-Strand Conformational Polymorphism. International Journal of Hematology 80:2, pages 136-139.
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Supap Boonsa, Kanokwan Sanchaisuriya, Goonnapa Fucharoen, Surapon Wiangnon, Arunee Jetsrisuparb & Supan Fucharoen. (2004) The Diverse Molecular Basis and Hematological Features of Hb H and AEBart’s Diseases in Northeast Thailand. Acta Haematologica 111:3, pages 149-154.
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Supan Fucharoen, Yossombat Changtrakun, Thawalwong Ratanasiri, Goonnapa Fucharoen & Kanokwan Sanchaisuriya. (2003) Complex interaction of Hb Hekinan [α27(B8) Glu-Asp] and Hb E [β26(B8) Glu-Lys] with a deletional α-thalassemia 1 in a Thai family. European Journal of Haematology 70:5, pages 304-309.
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David H. K. ChuiSuthat FucharoenVivian Chan. (2003) Hemoglobin H disease: not necessarily a benign disorder. Blood 101:3, pages 791-800.
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