ภาควิชากุมารเวชศาสตร์ | คณะแพทยศาสตร์ศิริราชพยาบาล มหาวิทยาลัยมหิดล

1.

Youngkong, S.; Thavorncharoensap, M.; Chaikledkaew, U.; Luangsinsiri, C.; Tim-Aroon, T.; Kuptanon, C.; Sathienkijkanchai, A.; Rojnueangnit, K.; Wichajarn, K.; Boonyawat, B.; Suphapeetiporn, K.; Wattanasirichaigoon, D.

Impacts and Economic Burden of Pompe Disease on Patients and Families in Thailand: A Mixed Method Study
ClinicoEconomics and Outcomes Research. 2026. 18 1-11.

2.

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

Posterior Cranial Decompression in ERF-Mutated Multisuture Craniosynostosis
J Craniofac Surg. 2026.

3.

Chaisrisawadisuk S, Khampalikit I, Sathienkijkanchai A.

Sagittal Craniosynostosis Associated With Chromosome 16p13.3 Duplication
J Craniofac Surg. 2026.

4.

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.

5.

Chaisrisawadisuk S, Tunkijjaroen T, Sathienkijkanchai A, Vatanavicharn N, Moore MH.

VACTERL Association and Unilateral Lambdoid Craniosynostosis
Cleft Palate Craniofacial Journal. 2025.

6.

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

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

7.

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):

8.

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

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

9.

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):

10.

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.

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