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

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.

INBORN ERRORS OF METABOLISM IN ASIA

JOURNAL OF INHERITED METABOLIC DISEASE.  2012.  35  (Suppl1): S169-S169.

Phenotypic and mutation spectrums of Thai patients with isovaleric acidemia
Pediatrics International.  2011.  53  (6): 990-994.

Glutaric aciduria type 2, late onset type in Thai siblings with myopathy
Pediatric Neurology.  2010.  43  (4): 279-282.

An infant with cartilage-hair hypoplasia due to a novel homozygous mutation in the promoter region of the RMRP gene associated with chondrodysplasia and severe immunodeficiency
Journal of Applied Genetics.  2010.  51  (4): 523-528.

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

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

Novel mutation affecting the pterin-binding site of PTS gene and review of PTS mutations in Thai patients with 6-pyruvoyltetrahydropterin synthase deficiency
Journal of Inherited Metabolic Disease.  2009.  1-4.

Down syndrome parents' support group in Thailand Siriraj Hospital, fifteen years experience: A review
Journal of the Medical Association of Thailand.  2009.  92  (9): 1256-1262.