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.

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

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):

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

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