ผลงานที่ได้รับการตีพิมพ์

รศ.นพ. นิธิวัชร์ วัฒนวิจารณ์

  • 31.
    Vatanavicharn N., Salazar D., Mekikian P.B., Wilcox W.R.
    Outcomes and complications of CPT1A deficiency observed during the long-term follow up of 4 cases
    Molecular Genetics and Metabolism.  2007.  90  (3):
  • 32.
    Wasant P., Liammongkolkul S., Sathienkijkarnchai A., Vatanavicharn N.
    Propionic acidemia in Thai infants: A report of 2 cases
    Journal of Inherited Metabolic Disease.  2006.  29  (Suppl 1):
  • 33.
    Vatanavicharn N., Graham J.M., Dawson K., Kohlase J.
    Discordant monozygotic twins with Wildervanck syndrome: A proposed mode of inheritance
    Journal of Investigetive Medicine.  2006.  54  S100-S100.
  • 34.
    Wasant P., Vatanavicharn N., Srisomsap C., Sawangareetrakul P., Liammongkolkul S., Svasti J.
    Retrospective study of patients with suspected inborn errors of metabolism at Siriraj Hospital, Bangkok, Thailand (1997-2001)
    Journal of the Medical Association of Thailand.  2005.  88  (6): 746-753.