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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1988 1
2004 1
2006 2
2009 1
2012 1
2021 0
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6 results
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Page 1
High prevalence of V37I genetic variant in the connexin-26 (GJB2) gene among non-syndromic hearing-impaired and control Thai individuals.
Wattanasirichaigoon D, Limwongse C, Jariengprasert C, Yenchitsomanus PT, Tocharoenthanaphol C, Thongnoppakhun W, Thawil C, Charoenpipop D, Pho-iam T, Thongpradit S, Duggal P. Wattanasirichaigoon D, et al. Among authors: charoenpipop d. Clin Genet. 2004 Nov;66(5):452-60. doi: 10.1111/j.1399-0004.2004.00325.x. Clin Genet. 2004. PMID: 15479191
Pericardial effusion in primary systemic carnitine deficiency.
Wattanasirichaigoon D, Khowsathit P, Visudtibhan A, Suthutvoravut U, Charoenpipop D, Kim SZ, Levy HL, Shih VE. Wattanasirichaigoon D, et al. Among authors: charoenpipop d. J Inherit Metab Dis. 2006 Aug;29(4):589. doi: 10.1007/s10545-006-0335-7. Epub 2006 Jul 8. J Inherit Metab Dis. 2006. PMID: 16830263
Novel missense mutations of SAR1B gene in an infant with chylomicron retention disease.
Treepongkaruna S, Chongviriyaphan N, Suthutvoravut U, Charoenpipop D, Choubtum L, Wattanasirichaigoon D. Treepongkaruna S, et al. Among authors: charoenpipop d. J Pediatr Gastroenterol Nutr. 2009 Mar;48(3):370-3. doi: 10.1097/mpg.0b013e318183188f. J Pediatr Gastroenterol Nutr. 2009. PMID: 19274794 No abstract available.