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Elife|May 24, 2019
Estimating the burden of α-thalassaemia in Thailand using a comprehensive prevalence database for Southeast AsiaCarinna Hockham, Supachai Ekwattanakit, Samir Bhatt, et al.
Annals of Hematology|May 16, 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 methodThanyachai Sura, Objoon Trachoo, Vip Viprakasit, et al.
Plos One|May 23, 2014
A normal reference of bone mineral density (BMD) measured by dual energy X-ray absorptiometry in healthy thai children and adolescents aged 5-18 years: a new reference for Southeast Asian PopulationsPairunyar Nakavachara, Julaporn Pooliam, Linda Weerakulwattana, et al.
Asian Pacific Journal of Allergy and Immunology|July 4, 2008
Successful treatment of disseminated BCG infection in a SCID patient with granulocyte colony stimulating factorWipada Pariyaprasert, Punchama Pacharn, Nualanong Visitsunthorn, et al.
Journal of the Medical Association of Thailand = Chotmaihet Thangphaet|October 31, 2002
Effect of red blood cell glucose-6-phosphate dehydrogenase deficiency on patients with dengue hemorrhagic feverVoravarn S Tanphaichitr, Rachaneekorn Chonlasin, Lerlugsn Suwantol, et al.
Mediterranean Journal of Hematology and Infectious Diseases|November 22, 2021
Long-Term Effectiveness, Safety, and Tolerability of Twice-Daily Dosing with Deferasirox in Children with Transfusion-Dependent Thalassemias Unresponsive to Standard Once-Daily DosingJassada Buaboonnam, Chayamon Takpradit, Vip Viprakasit, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|August 29, 2020
Using of deferasirox and deferoxamine in refractory iron overload thalassemiaChayamon Takpradit, Vip Viprakasit, Nattee Narkbunnam, et al.
Acta Haematologica|October 2, 2013
Clinical presentation and molecular identification of four uncommon alpha globin variants in Thailand. Initiation codon mutation of α2-globin Gene (HBA2:c.1delA), donor splice site mutation of α1-globin gene (IVSI-1, HBA1:c.95 + 1G>A), hemoglobin Queens Park/Chao Pra Ya (HBA1:c.98T>A) and hemoglobin Westmead (HBA2:c.369C>G)Vip Viprakasit, Supachai Ekwattanakit, Nipon Chalaow, et al.
Haematologica|February 12, 2002
Clinical phenotypes and molecular characterization of Hb H-Paksé diseaseVip Viprakasit, Voravarn S Tanphaichitr, Parichat Pung-Amritt, et al.
Hemoglobin|July 23, 2014
Incidence of ototoxicity in pediatric patients with transfusion-dependent thalassemia who are less well-chelated by mono- and combined therapy of iron chelating agentsArchwin Tanphaichitr, Thisarat Kusuwan, Siriporn Limviriyakul, et al.
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