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Journal of the Medical Association of Thailand = Chotmaihet Thangphaet|October 9, 2008
Factors influencing development of Down syndrome children in the first three years of life: Siriraj experiencePornswan Wasant, Boonchai Boonyawat, Samruay Tritilanunt, et al.
Biochemical Genetics|September 16, 2015
Analysis of Novel Mutations and Methylmalonyl-CoA Mutase Levels in Thai Patients with Isolated Methylmalonic AcidemiaPhannee Sawangareetrakul, James R Ketudat Cairns, Nithiwat Vatanavicharn, et al.
Brain & Development|December 3, 2014
Carnitine-acylcarnitine translocase deficiency: Two neonatal cases with common splicing mutation and in vitro bezafibrate responseNithiwat Vatanavicharn, Kenji Yamada, Yuka Aoyama, et al.
Biochemical Genetics|April 6, 2007
Novel mutations found in two genes of thai patients with isolated methylmalonic acidemiaSiriporn Keeratichamroen, James R Ketudat Cairns, Phannee Sawangareetrakul, et al.
Plos One|August 11, 2015
An Economic Evaluation of Neonatal Screening for Inborn Errors of Metabolism Using Tandem Mass Spectrometry in ThailandKittiphong Thiboonboon, Pattara Leelahavarong, Duangrurdee Wattanasirichaigoon, et al.
Molecular Biology Reports|March 7, 2021
Molecular characterization of Thai patients with phenylalanine hydroxylase deficiency and in vitro functional study of two novel PAH variantsLukana Ngiwsara, Nithiwat Vatanavicharn, Phannee Sawangareetrakul, et al.
The Southeast Asian Journal of Tropical Medicine and Public Health|January 28, 2006
The molecular basis of mucopolysaccharidosis type I in two Thai patientsJames R Ketudat Cairns, Siriporn Keeratichamroen, Supattra Sukcharoen, et al.
Molecular Genetics and Metabolism|June 15, 2012
Clinical and molecular findings in Thai patients with isolated methylmalonic acidemiaNithiwat Vatanavicharn, Voraratt Champattanachai, Somporn Liammongkolkul, et al.
International Journal of Molecular Sciences|June 27, 2024
Homozygosity for a Rare <i>Plec</i> Variant Suggests a Contributory Role in Congenital Insensitivity to PainPiranit Kantaputra, Teerada Daroontum, Kantapong Kitiyamas, et al.
Molecular Genetics and Metabolism|August 7, 2012
Current diagnosis and management of mucopolysaccharidosis VI in the Asia-Pacific regionWuh-Liang Hwu, Torayuki Okuyama, Wai Man But, et al.
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