Vatanavicharn N - Search Results

1

An Economic Evaluation of Neonatal Screening for Inborn Errors of Metabolism Using Tandem Mass Spectrometry in Thailand.

Thiboonboon K, Leelahavarong P, Wattanasirichaigoon D, Vatanavicharn N, Wasant P, Shotelersuk V, Pangkanon S, Kuptanon C, Chaisomchit S, Teerawattananon Y. Thiboonboon K, et al. Among authors: vatanavicharn n. PLoS One. 2015 Aug 10;10(8):e0134782. doi: 10.1371/journal.pone.0134782. eCollection 2015. PLoS One. 2015. PMID: 26258410 Free PMC article.

2

Retrospective study of patients with suspected inborn errors of metabolism at Siriraj Hospital, Bangkok, Thailand (1997-2001).

Wasant P, Vatanavicharn N, Srisomsap C, Sawangareetrakul P, Liammongkolkul S, Svasti J. Wasant P, et al. Among authors: vatanavicharn n. J Med Assoc Thai. 2005 Jun;88(6):746-53. J Med Assoc Thai. 2005. PMID: 16083213

3

Organic acid disorders detected by urine organic acid analysis: twelve cases in Thailand over three-year experience.

Wasant P, Liammongkolkul S, Kuptanon C, Vatanavicharn N, Sathienkijakanchai A, Shinka T. Wasant P, et al. Among authors: vatanavicharn n. Clin Chim Acta. 2008 Jun;392(1-2):63-8. doi: 10.1016/j.cca.2008.02.015. Epub 2008 Feb 23. Clin Chim Acta. 2008. PMID: 18339316

4

Factors influencing development of Down syndrome children in the first three years of life: Siriraj experience.

Wasant P, Boonyawat B, Tritilanunt S, Vatanavicharn N, Sathienkijakanchai A, Ratanarak P, Malilum O, Liammongkolkul S. Wasant P, et al. Among authors: vatanavicharn n. J Med Assoc Thai. 2008 Jul;91(7):1030-7. J Med Assoc Thai. 2008. PMID: 18839841

5

Novel mutation affecting the pterin-binding site of PTS gene and review of PTS mutations in Thai patients with 6-pyruvoyltetrahydropterin synthase deficiency.

Vatanavicharn N, Kuptanon C, Liammongkolkul S, Liu TT, Hsiao KJ, Ratanarak P, Blau N, Wasant P. Vatanavicharn N, et al. J Inherit Metab Dis. 2009 Dec;32 Suppl 1:S279-82. doi: 10.1007/s10545-009-1221-x. Epub 2009 Oct 13. J Inherit Metab Dis. 2009. PMID: 19830588 Review.

6

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.

Vatanavicharn N, Visitsunthorn N, Pho-iam T, Jirapongsananuruk O, Pacharn P, Chokephaibulkit K, Limwongse C, Wasant P. Vatanavicharn N, et al. J Appl Genet. 2010;51(4):523-8. doi: 10.1007/BF03208884. J Appl Genet. 2010. PMID: 21063072

7

Phenotypic and mutation spectrums of Thai patients with isovaleric acidemia.

Vatanavicharn N, Liammongkolkul S, Sakamoto O, Sathienkijkanchai A, Wasant P. Vatanavicharn N, et al. Pediatr Int. 2011 Dec;53(6):990-4. doi: 10.1111/j.1442-200X.2011.03488.x. Pediatr Int. 2011. PMID: 22004070

8

Amino acid disorders detected by quantitative amino acid HPLC analysis in Thailand: an eight-year experience.

Vatanavicharn N, Ratanarak P, Liammongkolkul S, Sathienkijkanchai A, Wasant P. Vatanavicharn N, et al. Clin Chim Acta. 2012 Jul 11;413(13-14):1141-4. doi: 10.1016/j.cca.2012.03.014. Epub 2012 Mar 23. Clin Chim Acta. 2012. PMID: 22465081

9

Clinical and molecular findings in Thai patients with isolated methylmalonic acidemia.

Vatanavicharn N, Champattanachai V, Liammongkolkul S, Sawangareetrakul P, Keeratichamroen S, Ketudat Cairns JR, Srisomsap C, Sathienkijkanchai A, Shotelersuk V, Kamolsilp M, Wattanasirichaigoon D, Svasti J, Wasant P. Vatanavicharn N, et al. Mol Genet Metab. 2012 Aug;106(4):424-9. doi: 10.1016/j.ymgme.2012.05.012. Epub 2012 May 29. Mol Genet Metab. 2012. PMID: 22695176

10

Clinical characteristics and mutation analysis of propionic acidemia in Thailand.

Vatanavicharn N, Liammongkolkul S, Sakamoto O, Kamolsilp M, Sathienkijkanchai A, Wasant P. Vatanavicharn N, et al. World J Pediatr. 2014 Feb;10(1):64-8. doi: 10.1007/s12519-014-0454-4. Epub 2014 Jan 25. World J Pediatr. 2014. PMID: 24464666

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