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21.

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.

22.

Wasant P., Liammongkolkul S., Kuptanon C., Vatanavicharn N., Sathienkijakanchai A., Shinka T.

Organic acid disorders detected by urine organic acid analysis: Twelve cases in Thailand over three-year experience
Clinica Chimica Acta. 2008. 392 (1-2): 63-68.

23.

Wasant P., Boonyawat B., Tritilanunt S., Vatanavicharn N., Sathienkijakanchai A., Ratanarak P., Malilum O., Liammongkolkul S.

Factors influencing development of down syndrome children in the first three years of life: Siriraj experience
Journal of the Medical Association of Thailand. 2008. 91 (7): 1030-1037.

24.

Keeratichamroen S., Ketudat Cairns J.R., Wattanasirichaigoon D., Wasant P., Ngiwsara L., Suwannarat P., Pangkanon S., Kuptanon J., Tanpaiboon P., Rujirawat T., Liammongkolkul S., Svasti J.

Molecular analysis of the iduronate-2-sulfatase gene in Thai patients with Hunter syndrome
Journal of Inherited Metabolic Disease. 2008. 1-9.

25.

Promkan M., Teingtat S., Stheinkijkarnchai A., Wasant P., Patmasiriwat P.

Highest accuracy of combined consensus clinical criteria and SNRPN gene molecular markers in diagnosis of Prader-Willi syndrome in Thai patients
Clinical Chemistry and Laboratory Medicine. 2007. 45 (8):

26.

Wasant P., Liammongkolkul S., Kuptanon C., Yamaguchi S.

Glutaric aciduria type II - late-onset form in Thai siblings - First reported cases in Thailand
Journal of Inherited Metabolic Disease . 2007. 30

27.

Wasant P., Liammongkolkul S., Kuptanon C., Yamaguchi S.

Primary systemic carnitine deficiency (SCD) in Thailand - A report of 2 cases
Journal of Inherited Metabolic Disease . 2007. 30

28.

Keeratichamroen S., Cairns J.R.K., Sawangareetrakul P., Liammongkolkul S., Champattanachai V., Srisomsap C., Kamolsilp M., Wasant P., Svasti J.

Novel mutations found in two genes of Thai patients with isolated methylmalonic acidemia
Biochemical Genetics. 2007. 45 (39238): 421-430.

29.

Wasant P., Liammongkolkul S., Ratanarak P.

A report of phenylketonuria in 2 Thai infants
Journal of Inherited Metabolic Disease. 2006. 29 (Suppl 1):

30.

Wasant P., Liammongkolkul S., Matsumoto I.

Alkaptonuria in a Thai infant: First reported case
Journal of Inherited Metabolic Disease. 2006. 29 (Suppl 1):

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