ภาควิชากุมารเวชศาสตร์ | คณะแพทยศาสตร์ศิริราชพยาบาล มหาวิทยาลัยมหิดล

1.

Rattanavipapong W.; Anothaisintawee T.; Isaranuwatchai W.; Wattanasirichaigoon D.; Tim-Aroon T.; Wichajarn K.; Sathienkijkanchai A.; Charoenkwan P.; Suphapeetiporn K.; Traivaree C.; Kuptanon C.; Teerawattananon Y.

Assessing the Value for Money of Enzyme Replacement Therapy in Gaucher Disease Types 1 and 3b: Can Expanded Coverage Be Justified?
PharmacoEconomics - Open. 2025.

2.

Chaisrisawadisuk S, Rattana-Arpa S, Vathanophas V, Sathienkijkanchai A.

Hyaline Fibromatosis Syndrome: Early Outcomes Following Major Craniofacial Mass Excision
Journal of Craniofacial Surgery. 2024.

3.

Kantaputra P.; Daroontum T.; Kitiyamas K.; Piyakhunakorn P.; Kawasaki K.; Sathienkijkanchai A.; Wasant P.; Vatanavicharn N.; Yasanga T.; Kaewgahya M.; Tongsima S.; Cox T.C.; Arold S.T.; Ohazama A.; Ngamphiw C.

Homozygosity for a Rare Plec Variant Suggests a Contributory Role in Congenital Insensitivity to Pain
International Journal of Molecular Sciences. 2024. 25 (12):

4.

Chaisrisawadisuk S, Khampalikit I, Moore MH, Sathienkijkanchai A.

Metopic and Sagittal Craniosynostosis in Williams Syndrome
J Craniofac Surg. 2023.

5.

Phetthong T., Tim-Aroon T., Khongkraparn A., Noojarern S., Kuptanon C., Wichajarn K., Sathienkijkanchai A., Suphapeetiporn K., Charoenkwan P., Tantiworawit A., Noentong N., Wattanasirichaigoon D.

Gaucher disease: clinical phenotypes and refining GBA mutational spectrum in Thai patients
Orphanet Journal of Rare Diseases. 2021. 16 (1):

6.

Suksawat Y., Sathienkijkanchai A., Veskitkul J., Jirapongsananuruk O., Visitsunthorn N., Vichyanond P., Pacharn P.

Resolution of Primary Immune Defect in 22q11.2 Deletion Syndrome
Journal of Clinical Immunology. 2017. 37 (4): 375-382.

7.

Vatanavicharn N., Liammongkolkul S., Sakamoto O., Kamolsilp M., Sathienkijkanchai A., Wasant P.

Clinical characteristics and mutation analysis of propionic acidemia in Thailand
World Journal of Pediatrics. 2014. 10 (1): 64-68.

8.

Vatanavicharn N, Yamada K, Aoyama Y, Fukao T, Densupsoontorn N, Jirapinyo P, Sathienkijkanchai A, Yamaguchi S, Wasant P.

Carnitine-acylcarnitine translocase deficiency: Two neonatal cases with common splicing mutation and in vitro bezafibrate response.
Brain Dev. 2014.

9.

Vatanavicharn, N. Champattanachai, V. Liammongkolkul, S. Sawangareetrakul, P. Keeratichamroen, S. Ketudat Cairns, J. R. Srisomsap, C. Sathienkijkanchai, A. Shotelersuk, V. Kamolsilp, M. Wattanasirichaigoon, D. Svasti, J. Wasant, P.

Clinical and molecular findings in Thai patients with isolated methylmalonic acidemia
MOLECULAR GENETICS AND METABOLISM. 2012. 106 (4): 424-429.

10.

Vatanavicharn, N; Ratanarak, P; Liammongkolkul, S; Sathienkijkanchai, A; Wasant, P

Amino acid disorders detected by quantitative amino acid HPLC analysis in Thailand: An eight-year experience
CLINICA CHIMICA ACTA. 2012. 413 (13-14): 1141-1141 1144.

ผลงานที่ได้รับการตีพิมพ์

ผศ.พญ. อัจฉรา เสถียรกิจการชัย