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Transfusion Medicine (Oxford, England)|September 30, 2023
How do we translate gaps and unmet needs of blood management for thalassemia into a collaborative implementation framework?Chanin Limwongse, Ponlapat Rojnuckarin, Pawinee Kupatawintu, et al.
Journal of the Medical Association of Thailand = Chotmaihet Thangphaet|July 5, 2011
Genetic polymorphism of low-density lipoprotein receptor did not affect treatment outcome of chronic hepatitis C genotype 3Tawesak Tanwandee, Manop Pithukpakorn, Noppawan Vipatakul, et al.
Dementia and Geriatric Cognitive Disorders Extra|May 31, 2021
Etiology of Dementia in Thai PatientsPornpatr A Dharmasaroja, Jintana Assanasen, Sunsanee Pongpakdee, et al.
Clinical and Translational Science|September 18, 2025
Bridging Pharmacokinetics and Pharmacodynamics: A PBPK/PD Model-Based Approach for Deferasirox Dosing in Transfusion-Dependent ThalassemiaWatchara Sakares, Udomsak Udomnilobol, Xian Pan, et al.
Human Mutation|May 20, 2008
Thailand mutation and variation database (ThaiMUT)Uttapong Ruangrit, Metawee Srikummool, Anunchai Assawamakin, et al.
Clinical Neurology and Neurosurgery|June 5, 2009
Novel DYSF mutations in Thai patients with distal myopathyTeerin Liewluck, Sunsanee Pongpakdee, Rawiphan Witoonpanich, et al.
Antiviral Therapy|December 14, 2011
Pharmacokinetics and safety of a new paediatric fixed-dose combination of zidovudine/lamivudine/nevirapine in HIV-infected childrenKulkanya Chokephaibulkit, Tim R Cressey, Edmund Capparelli, et al.
Human Genetics|April 22, 2010
Genome-wide linkage scan and association study of PARL to the expression of LHON families in ThailandNopasak Phasukkijwatana, Bussaraporn Kunhapan, Jim Stankovich, et al.
NPJ Genomic Medicine|February 14, 2024
Germline mutations of 4567 patients with hereditary breast-ovarian cancer spectrum in ThailandChalermkiat Kansuttiviwat, Pongtawat Lertwilaiwittaya, Ekkapong Roothumnong, et al.
Hematology (Amsterdam, Netherlands)|March 20, 2023
Whole exome sequencing and rare variant association study to identify genetic modifiers, <i>KLF1</i> mutations, and a novel double mutation in Thai patients with hemoglobin E/beta-thalassemiaChattree Hantaweepant, Bhoom Suktitipat, Manop Pithukpakorn, et al.
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