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Year Number of Results
2011 1
2015 3
2016 1
2017 5
2018 1
2019 5
2020 10
2021 2
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24 results
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Page 1
Klinefelter Syndrome Mosaicism 46,XX/47,XXY: A New Case and Literature Review.
Tangshewinsirikul C, Dulyaphat W, Tim-Aroon T, Parinayok R, Chareonsirisuthigul T, Korkiatsakul V, Waisayarat J, Sirisreetreerux P, Tingthanatikul Y, Wattanasirichaigoon D. Tangshewinsirikul C, et al. Among authors: tim aroon t. J Pediatr Genet. 2020 Dec;9(4):221-226. doi: 10.1055/s-0040-1713002. Epub 2020 Jun 17. J Pediatr Genet. 2020. PMID: 32733741
Two infants with abetalipoproteinemia: Classic versus atypical presentation.
Prachasitthisak N, Tanpowpong P, Tim-Aroon T, Treepongkaruna S, Chongviriyaphan N, Vithayasai N, Iamopas O, Wattanasirichaigoon D. Prachasitthisak N, et al. Among authors: tim aroon t. Pediatr Int. 2019 May;61(5):508-509. doi: 10.1111/ped.13822. Epub 2019 May 14. Pediatr Int. 2019. PMID: 31087595 No abstract available.
Growth charts for Thai children with Prader-Willi syndrome aged 0-18 years.
Mongkollarp N, Tim-Aroon T, Okascharoen C, Wichajarn K, Phosuwattanakul J, Chongviriyaphan N, Wattanasirichaigoon D. Mongkollarp N, et al. Among authors: tim aroon t. Orphanet J Rare Dis. 2020 May 6;15(1):111. doi: 10.1186/s13023-020-01388-7. Orphanet J Rare Dis. 2020. PMID: 32375863 Free PMC article.
Etiologies, Prognostic Factors, and Outcomes of Pediatric Acute Liver Failure in Thailand.
Getsuwan S, Lertudomphonwanit C, Tanpowpong P, Thirapattaraphan C, Tim-Aroon T, Wattanasirichaigoon D, Treepongkaruna S. Getsuwan S, et al. Among authors: tim aroon t. Pediatr Gastroenterol Hepatol Nutr. 2020 Nov;23(6):539-547. doi: 10.5223/pghn.2020.23.6.539. Epub 2020 Nov 5. Pediatr Gastroenterol Hepatol Nutr. 2020. PMID: 33215025 Free PMC article.
Clinical delineation of 18q11-q12 microdeletion: Intellectual disability, speech and behavioral disorders, and conotruncal heart defects.
Rojnueangnit K, Charalsawadi C, Thammachote W, Pradabmuksiri A, Tim-Aroon T, Novelli A, Loddo S, Briuglia S, Concetta CM, Wattanasirichaigoon D, Jinawath N. Rojnueangnit K, et al. Among authors: tim aroon t. Mol Genet Genomic Med. 2019 Sep;7(9):e896. doi: 10.1002/mgg3.896. Epub 2019 Aug 7. Mol Genet Genomic Med. 2019. PMID: 31390163 Free PMC article. Clinical Trial.
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: tim aroon t. Endocr Connect. 2020 Nov;9(11):1121-1134. doi: 10.1530/EC-20-0411. Endocr Connect. 2020. PMID: 33310921 Free PMC article.
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