ภาควิชากุมารเวชศาสตร์ | คณะแพทยศาสตร์ศิริราชพยาบาล มหาวิทยาลัยมหิดล

11.

Vatanavicharn, N; Champattanachai, V; Liammongkolkul, S; Sawangareetrakul, P; Keeratichamroen, S; Cairns, JRK; Srisomsap, C; Sathienkijkanchai, A; Svasti, J; Wasant, P

GENETIC ANALYSIS OF MUT, MMAA, AND MMAB IN THAI PATIENTS WITH ISOLATED METHYLMALONIC ACIDEMIA
JOURNAL OF INHERITED METABOLIC DISEASE. 2010. 33 S42-S42.

12.

Wasant, P; Sathienkijkanchai, A; Vattanavicham, N; Liammongkolkul, S; Keeratichamroen, S; Ketudat-Cairns, JR; Svasti, J; Kolodny, EH

MUCOPOLYSACCHARIDOSES IN THAILAND: SIRIRAJ EXPERIENCE
JOURNAL OF INHERITED METABOLIC DISEASE. 2010. 33 S138-S138.

13.

Goldfarb, C. A. Sathienkijkanchai, A. Robin, N. H.

Amniotic constriction band: a multidisciplinary assessment of etiology and clinical presentation
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME. 2009. 91 Suppl 4 68-75.

14.

Messiaen, L. Yao, S. Brems, H. Callens, T. Sathienkijkanchai, A. Denayer, E. Spencer, E. Arn, P. Babovic-Vuksanovic, D. Bay, C. Bobele, G. Cohen, B. H. Escobar, L. Eunpu, D. Grebe, T. Greenstein, R. Hachen, R. Irons, M. Kronn, D. Lemire, E. Leppig, K. Lim, C. McDonald, M. Narayanan, V. Pearn, A. Pedersen, R. Powell, B. Shapiro, L. R. Skidmore, D. Tegay, D. Thiese, H. Zackai, E. H. Vijzelaar, R. Taniguchi, K. Ayada, T. Okamoto, F. Yoshimura, A. Parret, A. Korf, B. Legius, E.

Clinical and mutational spectrum of neurofibromatosis type 1-like syndrome
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION. 2009. 302 (19): 2111-2118.

15.

Wasant, P; Liammongkolkul, S; Vattanavicharn, N; Sathienkijkanchai, A; Shinka, T

FUMARASE DEFICIENCY IN A THAI INFANT
MOLECULAR GENETICS AND METABOLISM. 2009. 98 (1-2): 635-635.

16.

Sathienkijkanchai A., Prucka S.K., Grant J.H., Robin N.H.

Isolated facial hemihyperplasia: Manifestation of beckwith-wiedemann syndrome
Journal of Craniofacial Surgery. 2008. 19 (1): 279-283.

17.

Mikhail F.M., Sathienkijkanchai A., Robin N.H., Prucka S., Biggerstaff J.S., Komorowski J., Andersson R., Bruder C.E., Piotrowski A., de St?hl T.D., Dumanski J.P., Carroll A.J.

Overlapping phenotype of Wolf-Hirschhorn and Beckwith-Wiedemann syndromes in a girl with der(4)t(4;11)(pter;pter
American Journal of Medical Genetics. 2007. 143 (15):

18.

Robin N.H., Sathienkijkanchai A., Anthony Herndon C.D.

A genetic model for cloacal exstrophy, the extreme cloacal malformation
Journal of Pediatric Urology. 2007. 3 (3):

19.

Wasant P., Sathienkijkanchai A.

Congenital defect of glycosylation (CDG) in Thai infants: Report of 2 cases
Journal of Inherited Metabolic Disease. 2006. 29 (Suppl 1):

20.

Wasant P., Liammongkolkul S., Ratanarak P., Sathienkijkanchai A., Watanavicharn N.

Nonketotic hyperglycinemia in Thai infants: Report of 5 cases
Journal of Inherited Metabolic Disease. 2006. 29 (Suppl 1):

ผลงานที่ได้รับการตีพิมพ์

ผศ.พญ. อัจฉรา เสถียรกิจการชัย