Two novel splice mutations of P gene in a Thai-Chinese patient with oculocutaneous albinism type II (OCA2)

بواسطة Duangrurdee Wattanasirichaigoon, Pim Suwannarat, Supranee Thongpradit
منشور في 2018

Gut microbiota characteristics in children after the use of proton pump inhibitors

بواسطة Lila Simakachorn, Pornthep Tanpowpong, Suwanee Chanprasertyothin, Supranee Thongpradit, Suporn Treepongkaruna
منشور في 2022

Effects of 8-Year Treatment of Long-Acting Testosterone Undecanoate on Metabolic Parameters, Urinary Symptoms, Bone Mineral Density, and Sexual Function in Men With Late-Onset Hypo...

بواسطة Sompol Permpongkosol, Kalayanee Khupulsup, Supatra Leelaphiwat, Sarawan Pavavattananusorn, Supranee Thongpradit, Thanom Petchthong
منشور في 2018

The Detection of SARS-CoV2 Antigen in Wastewater Using an Automated Chemiluminescence Enzyme Immunoassay

بواسطة Supranee Thongpradit, Somsak Prasongtanakij, Supanart Srisala, Suwannee Chanprasertyothin, Ekawat Pasomsub, Boonsong Ongphiphadhanakul
منشور في 2022

MITF variants cause nonsyndromic sensorineural hearing loss with autosomal recessive inheritance

بواسطة Supranee Thongpradit, Natini Jinawath, Asif Javed, Saisuda Noojarern, Arthaporn Khongkraparn, Thipwimol Tim-Aroon, Krisna Lertsukprasert, Bhoom Suktitipat, Laran T. Jensen, Duangrurdee Wattanasirichaigoon
منشور في 2020

Novel SOX10 Mutations in Waardenburg Syndrome: Functional Characterization and Genotype-Phenotype Analysis

بواسطة Supranee Thongpradit, Natini Jinawath, Asif Javed, Laran T. Jensen, Issarapa Chunsuwan, Kitiwan Rojnueangnit, Thipwimol Tim-Aroon, Krisna Lertsukprasert, Meng Shin Shiao, Nongnuch Sirachainan, Duangrurdee Wattanasirichaigoon
منشور في 2021

A Simple Method to Detect SARS-CoV-2 in Wastewater at Low Virus Concentration

بواسطة Supranee Thongpradit, Somsak Prasongtanakij, Supanart Srisala, Yothin Kumsang, Suwannee Chanprasertyothin, Pairoj Boonkongchuen, Dhanesh Pitidhammabhorn, Parnrudee Manomaipiboon, Peeraya Somchaiyanon, Siriwan Chandanachulaka, Taiyatach Hirunrueng, Boonsong Ongphiphadhanakul
منشور في 2022

Infantile onset Sandhoff disease: clinical manifestation and a novel common mutation in Thai patients

بواسطة Thipwimol Tim-Aroon, Khunton Wichajarn, Kamornwan Katanyuwong, Pranoot Tanpaiboon, Nithiwat Vatanavicharn, Kullasate Sakpichaisakul, Arthaporn Kongkrapan, Jakris Eu-ahsunthornwattana, Supranee Thongpradit, Kanya Moolsuwan, Nusara Satproedprai, Surakameth Mahasirimongkol, Tassanee Lerksuthirat, Bhoom Suktitipat, Natini Jinawath, Duangrurdee Wattanasirichaigoon
منشور في 2022