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Browsing by Author Kanda Fanhchaksai

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Issue DateTitleAuthor(s)
1-Jun-2020Leukocyte telomere length in patients with transfusion-dependent thalassemiaNithita Nanthatanti; Adisak Tantiworawit; Pokpong Piriyakhuntorn; Thanawat Rattanathammethee; Sasinee Hantrakool; Chatree Chai-Adisaksopha; Ekarat Rattarittamrong; Lalita Norasetthada; Wirote Tuntiwechapikul; Kanda Fanhchaksai; Pimlak Charoenkwan; Sirinart Kumfu; Nipon Chattipakorn
1-Jan-2022The Long-Term Efficacy of Deferiprone in Thalassemia Patients With Iron Overload: Real-World Data from the Registry DatabaseTeerajed Kittipoom; Adisak Tantiworawit; Teerachat Punnachet; Nonthakorn Hantrakun; Pokpong Piriyakhuntorn; Thanawat Rattanathammethee; Sasinee Hantrakool; Chatree Chai-Adisaksopha; Ekarat Rattarittamrong; Lalita Norasetthada; Kanda Fanhchaksai; Pimlak Charoenkwan
1-Jan-2018Novel mutations in SPTA1 and SPTB identified by whole exome sequencing in eight Thai families with hereditary pyropoikilocytosis presenting with severe fetal and neonatal anaemiaChupong Ittiwut; Rungrote Natesirinilkul; Fuanglada Tongprasert; Lalita Sathitsamitphong; Chane Choed-amphai; Kanda Fanhchaksai; Pimlak Charoenkwan; Kanya Suphapeetiporn; Vorasuk Shotelersuk
1-Jan-2019A randomized, open-labeled, prospective controlled study to assess the efficacy of frontline empirical intravenous piperacillin/tazobactam monotherapy in comparison with ceftazidime plus amikacin for febrile neutropenia in pediatric oncology patientsRuchirek Kamonrattana; Lalita Sathitsamitphong; Worawut Choeyprasert; Pimlak Charoenkwan; Rungrote Natesirinilkul; Kanda Fanhchaksai
1-Aug-2021Severe neonatal haemolytic anaemia caused by compound heterozygous KLF1 mutations: report of four families and literature reviewTanu Tangsricharoen; Rungrote Natesirinilkul; Arunee Phusua; Kanda Fanhchaksai; Chupong Ittiwut; Wanna Chetruengchai; Monthana Juntharaniyom; Pimlak Charoenkwan; Vip Viprakasit; Chureerat Phokaew; Vorasuk Shotelersuk
Showing results 16 to 20 of 20 < previous