Browsing by Author Chupong Ittiwut

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
or enter first few letters:  
Showing results 1 to 7 of 7
Issue DateTitleAuthor(s)
1-Jul-2021Coinherited Hemoglobin H/Constant Spring Disease and Heterozygous Hemoglobin Tak Causing Severe Hemolytic Anemia in a Thai BoyChane Choed-Amphai; Arunee Phusua; Chupong Ittiwut; Pimlak Charoenkwan; Kanya Suphapeetiporn; Vorasuk Shotelersuk
1-Jan-2019Discrepancy in the degree of polycythemia in a family with a novel nonsense EPOR mutationChitsanupong Ratarat; Chupong Ittiwut; Rungrote Natesirinilkul; Lalita Sathitsamitpong; Kanda Fanhchaksai; Pimlak Charoenkwan; Kanya Suphapeetiporn; Vorasuk Shotelersuk
1-Jan-2022Genetic basis of sudden death after COVID-19 vaccination in ThailandChupong Ittiwut; Surakameth Mahasirimongkol; Smith Srisont; Rungnapa Ittiwut; Manoch Chockjamsai; Piya Durongkadech; Waritta Sawaengdee; Athiwat Khunphon; Kanidsorn Larpadisorn; Sukanya Wattanapokayakit; Suppachok Wetchaphanphesat; Surachet Arunotong; Suphot Srimahachota; Chakrarat Pittayawonganon; Panithee Thammawijaya; Derek Sutdan; Pawinee Doungngern; Apichai Khongphatthanayothin; Stephen J. Kerr; Vorasuk Shotelersuk
16-Sep-2017Massive parallel sequencing as a new diagnostic approach for phenylketonuria and tetrahydrobiopterin-deficiency in ThailandPongsathorn Chaiyasap; Chupong Ittiwut; Chalurmpon Srichomthong; Apiruk Sangsin; Kanya Suphapeetiporn; Vorasuk Shotelersuk
1-Jan-2019A Novel GNAS Mutation Causing Isolated Infantile Cushing's SyndromePrapai Dejkhamron; Chupong Ittiwut; Hataitip Tangngam; Kanokkarn Sunkonkit; Rungrote Natesirinilkul; Kanya Suphapeetiporn; Vorasuk Shotelersuk
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-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