A First Case Report of Subependymoma in PTPN11 Mutation-Associated Noonan Syndrome by Boonchai Boonyawat, Mongkon Charoenpitakchai, Piradee Suwanpakdee

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Genotype-Phenotype Correlation of G6PD Mutations among Central Thai Children with G6PD Deficiency by Boonchai Boonyawat, Tim Phetthong, Nithipun Suksumek, Chanchai Traivaree

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Recurrent Rhabdomyolysis in a Medical Cadet during Military Training as a Rare Initial Presentation in Calpainopathy by Sethapong Lertsakulbunlue, Boonsub Sakboonyarat, Piradee Suwanpakdee, Boonchai Boonyawat

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X-Linked Chronic Granulomatous Disease: Initial Presentation with Intracranial Hemorrhage from Vitamin K Deficiency in Infant by Boonchai Boonyawat, Yiwa Suksawat, Punchama Pacharn, Piradee Suwanpakdee, Chanchai Traivaree

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Exploring molecular spectrum in thai patients with maple syrup urine disease: unveiling a common variant by Panisara Lakkhana, Thipwimol Tim-Aroon, Arthaporn Khongkraparn, Saisuda Noojarern, Parith Wongkittichote, Khunton Wichajarn, Chulaluck Kuptanon, Boonchai Boonyawat, Kanya Suphapeetiporn, Karn Wejaphikul, GoHun Seo, Duangrurdee Wattanasirichaigoon

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