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

Year Number of Results
1990 1
1993 4
1994 2
1997 3
1998 1
1999 5
2000 1
2002 4
2003 2
2004 2
2005 3
2006 2
2007 1
2008 1
2009 4
2010 7
2011 7
2012 3
2013 5
2014 3
2015 2
2016 2
2017 5
2018 7
2019 5
2020 5
2021 2
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73 results
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Page 1
Under-recognized Hypoparathyroidism in Thalassemia.
Tangngam H, Mahachoklertwattana P, Poomthavorn P, Chuansumrit A, Sirachainan N, Chailurkit L, Khlairit P. Tangngam H, et al. Among authors: mahachoklertwattana p. J Clin Res Pediatr Endocrinol. 2018 Nov 29;10(4):324-330. doi: 10.4274/jcrpe.0020. Epub 2018 May 4. J Clin Res Pediatr Endocrinol. 2018. PMID: 29726397 Free PMC article.
Eponym : de Quervain thyroiditis.
Engkakul P, Mahachoklertwattana P, Poomthavorn P. Engkakul P, et al. Among authors: mahachoklertwattana p. Eur J Pediatr. 2011 Apr;170(4):427-31. doi: 10.1007/s00431-010-1306-4. Epub 2010 Oct 1. Eur J Pediatr. 2011. PMID: 20886353 Review.
DUOX2 variants are a frequent cause of congenital primary hypothyroidism in Thai patients.
Sorapipatcharoen K, Tim-Aroon T, Mahachoklertwattana P, Chantratita W, Iemwimangsa N, Sensorn I, Panthan B, Jiaranai P, Noojarern S, Khlairit P, Pongratanakul S, Suprasongsin C, Korwutthikulrangsri M, Sriphrapradang C, Poomthavorn P. Sorapipatcharoen K, et al. Among authors: mahachoklertwattana p. Endocr Connect. 2020 Nov;9(11):1121-1134. doi: 10.1530/EC-20-0411. Endocr Connect. 2020. PMID: 33310921 Free PMC article.
Effect of vitamin D on lung function assessed by forced oscillation technique in asthmatic children with vitamin D deficiency: A randomized double-blind placebo-controlled trial.
Swangtrakul N, Manuyakorn W, Mahachoklertwattana P, Kiewngam P, Sasisakulporn C, Jotikasthirapa W, Kamchaisatian W, Benjaponpitak S. Swangtrakul N, et al. Among authors: mahachoklertwattana p. Asian Pac J Allergy Immunol. 2019 Dec 14. doi: 10.12932/AP-010519-0553. Online ahead of print. Asian Pac J Allergy Immunol. 2019. PMID: 31837209 Free article.
Successful parathyroidectomy with intra-operative parathyroid hormone monitoring in a neonate with severe primary hyperparathyroidism caused by homozygous mutation in CASR gene.
Sorapipatcharoen K, Mahachoklertwattana P, Tim-Aroon T, Wattanasirichaigoon D, Karanes S, Molagool S, Poomthavorn P. Sorapipatcharoen K, et al. Among authors: mahachoklertwattana p. J Paediatr Child Health. 2020 Jul;56(7):1144-1146. doi: 10.1111/jpc.14757. Epub 2019 Dec 28. J Paediatr Child Health. 2020. PMID: 31883284 No abstract available.
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