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

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

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.

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

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.

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.

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

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