Thanatophoric dysplasia: Roentgenographic findings and detection of a de novo mutation of FGFR3 gene in a Thai patient

by Duangrurdee Wattanasirichaigoon, Dussadee Charoenpipop
Published 2018

Strokes in Thai children : Etiology and outcome

by Pongsakdi Visudhiphan, Surang Chiemchanya, Duangrurdee Wattanasirichaigoon
Published 2018

A Novel Homozygous PKP2 Variant in Severe Neonatal Non-compaction and Concomitant Ventricular Septal Defect: A Case Report

by Poomiporn Katanyuwong, Arthaporn Khongkraparn, Duangrurdee Wattanasirichaigoon
Published 2022

5'UTR Repeat Polymorphisms of the BMPR2 gene in Children with Pulmonary Hypertension associated with Congenital Heart Disease

by Alisa Limsuwan, Lulin Choubtum, Duangrurdee Wattanasirichaigoon
Published 2018

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

by Duangrurdee Wattanasirichaigoon, Pim Suwannarat, Supranee Thongpradit
Published 2018

A new case of maternal lupus-associated chondrodysplasia punctata with extensive spinal anomalies

by Thipwimol Tim-aroon, Suphaneewan Jaovisidha, Duangrurdee Wattanasirichaigoon
Published 2018

Isolated lissencephaly sequence with contiguous gene deletion detected by FISH analysis: A case report

by Duangrurdee Wattanasirichaigoon, Chintana Tocharoenthanaphol, Anannit Visudtibhan, Surang Chiemchanya
Published 2018

Clinical and laboratory findings and outcomes of classic organic acidurias in children from north-eastern Thailand: A 5-year retrospective study

by Khunton Wichajarn, Somporn Liammongkolkul, Nithiwat Vatanavicharn, Duangrurdee Wattanasirichaigoon
Published 2018

Prediction of the functional effect of novel SLC25A13 variants using a S. cerevisiae model of AGC2 deficiency

by Parith Wongkittichote, Sumalee Tungpradabkul, Duangrurdee Wattanasirichaigoon, Laran T. Jensen
Published 2018

Mutations of ATP7B gene in two Thai siblings with Wilson disease

by Suporn Treepongkaruna, Paneeya Pienvichit, Pornpimon Phuapradit, Porawee Kodcharin, Duangrurdee Wattanasirichaigoon
Published 2018

Expanding the phenotypic spectrum of Lenz-Majewski syndrome: Facial palsy, cleft palate and hydrocephalus

by Duangrurdee Wattanasirichaigoon, Anannit Visudtibhan, Suphaneewan Jaovisidha, Jiraporn Laothamatas, Amornsri Chunharas
Published 2018

Carnitine levels and cardiac functions in children with solid malignancies receiving doxorubicin therapy

by Anant Khositseth, Suwadee Jirasakpisarn, Samart Pakakasama, Lulin Choubtuym, Duangrurdee Wattanasirichaigoon
Published 2018

Development of food products using fish maw (Pangasius hypophthalmus) and roasted sunflower kernel (Helianthus annuus) for branched-chain organic acidurias patients

by Suthida Chatvuttinun, Visith Chavasit, Duangrurdee Wattanasirichaigoon, Umaporn Suthutvoravut, Nalinee Chongviriyaphan
Published 2019

A novel mutation of cystathionine β-synthase gene in a thai boy with homocystinuria

by Nongnuch Sirachainan, Duangrurdee Wattanasirichaigoon, Pim Suwannarat, Werasak Sasanakul, Ampaiwan Chuansumrit
Published 2018

Correction to: Perspectives of adults with Klinefelter syndrome, unaffected adolescent males, and parents of affected children toward diagnosis disclosure: a Thai experience (Journ...

by Sukrit Suwannachat, Duangrurdee Wattanasirichaigoon, Jiraporn Arunakul, Vilawan Chirdkiatgumchai, Thipwimol Tim-Aroon
Published 2020

Genotype and age at diagnosis in Thai boys with Duchenne muscular dystrophy (DMD)

by Pattareeya Yamputchong, Theeraphong Pho-iam, Chanin Limwongse, Duangrurdee Wattanasirichaigoon, Oranee Sanmaneechai
Published 2020

Compound heterozygote of point mutation and chromosomal microdeletion involving otud6b coinciding with zmiz1 variant in syndromic intellectual disability

by Tim Phetthong, Arthaporn Khongkrapan, Natini Jinawath, Go Hun Seo, Duangrurdee Wattanasirichaigoon
Published 2022

Perspectives of adults with Klinefelter syndrome, unaffected adolescent males, and parents of affected children toward diagnosis disclosure: a Thai experience

by Sukrit Suwannachat, Duangrurdee Wattanasirichaigoon, Jiraporn Arunakul, Vilawan Chirdkiatgumchai, Thipwimol Tim-Aroon
Published 2020

Whole Exome Sequencing Revealing RYR1 Pathogenic Variant in an Exceptional Family with Malignant Hyperthermia Susceptibility

by Arthaporn Khongkraparn, Nitcha Khunin, Thipwimol Tim-Aroon, Tanit Virankabutra, Duangrurdee Wattanasirichaigoon
Published 2022

Kabuki syndrome with midgut malrotation and hyperinsulinemic hypoglycemia: A rare co-occurrence from Thailand

by Tim Phetthong, Thipwimol Tim-Aroon, Arthaporn Khongkrapan, Preamrudee Poomthavorn, Duangrurdee Wattanasirichaigoon
Published 2020