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

Year Number of Results
2001 3
2002 1
2003 2
2007 1
2008 1
2010 1
2011 4
2012 1
2014 1
2015 2
2016 3
2017 6
2018 5
2019 6
2020 10
2021 7
2022 3
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47 results
Results by year
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Page 1
Whole-Exome Sequencing Solved over 2-Decade Kidney Disease Enigma.
Isaranuwatchai S, Chanakul A, Ittiwut C, Srichomthong C, Shotelersuk V, Praditpornsilpa K, Suphapeetiporn K. Isaranuwatchai S, et al. Among authors: ittiwut c. Nephron. 2021;145(3):311-316. doi: 10.1159/000514293. Epub 2021 Mar 16. Nephron. 2021. PMID: 33725694
Targeted therapies for rare gynaecological cancers.
Manchana T, Ittiwut C, Mutirangura A, Kavanagh JJ. Manchana T, et al. Among authors: ittiwut c. Lancet Oncol. 2010 Jul;11(7):685-93. doi: 10.1016/S1470-2045(09)70368-7. Epub 2010 Mar 31. Lancet Oncol. 2010. PMID: 20362508 Review.
Expanding phenotypic and mutational spectra of mitochondrial HMG-CoA synthase deficiency.
Rojnueangnit K, Maneechai P, Thaweekul P, Piriyanon P, Khositseth S, Ittiwut C, Chetruengchai W, Kamolvisit W, Theerapanon T, Suphapeetiporn K, Porntaveetus T, Shotelersuk V. Rojnueangnit K, et al. Among authors: ittiwut c. Eur J Med Genet. 2020 Dec;63(12):104086. doi: 10.1016/j.ejmg.2020.104086. Epub 2020 Oct 9. Eur J Med Genet. 2020. PMID: 33045405
Whole exome sequencing for diagnosis of hereditary thrombocytopenia.
Mekchay P, Ittiwut C, Ittiwut R, Akkawat B, Le Grand SM, Leela-Adisorn N, Muanpetch S, Khovidhunkit W, Sosothikul D, Shotelersuk V, Suphapeetiporn K, Rojnuckarin P. Mekchay P, et al. Among authors: ittiwut c. Medicine (Baltimore). 2020 Nov 20;99(47):e23275. doi: 10.1097/MD.0000000000023275. Medicine (Baltimore). 2020. PMID: 33217855 Free PMC article.
A novel PITX2 mutation in non-syndromic orodental anomalies.
Intarak N, Theerapanon T, Ittiwut C, Suphapeetiporn K, Porntaveetus T, Shotelersuk V. Intarak N, et al. Among authors: ittiwut c. Oral Dis. 2018 May;24(4):611-618. doi: 10.1111/odi.12804. Epub 2018 Mar 13. Oral Dis. 2018. PMID: 29121437
Severe neonatal haemolytic anaemia caused by compound heterozygous KLF1 mutations: report of four families and literature review.
Tangsricharoen T, Natesirinilkul R, Phusua A, Fanhchaksai K, Ittiwut C, Chetruengchai W, Juntharaniyom M, Charoenkwan P, Viprakasit V, Phokaew C, Shotelersuk V. Tangsricharoen T, et al. Among authors: ittiwut c. Br J Haematol. 2021 Aug;194(3):626-634. doi: 10.1111/bjh.17616. Epub 2021 Jul 5. Br J Haematol. 2021. PMID: 34227100
Rapid exome sequencing as the first-tier investigation for diagnosis of acutely and severely ill children and adults in Thailand.
Kamolvisit W, Phowthongkum P, Boonsimma P, Kuptanon C, Rojnueangnit K, Wattanasirichaigoon D, Chanvanichtrakool M, Phuaksaman C, Wiromrat P, Srichomthong C, Ittiwut C, Phokaew C, Ittiwut R, Assawapitaksakul A, Chetruengchai W, Buasong A, Suphapeetiporn K, Shotelersuk V. Kamolvisit W, et al. Among authors: ittiwut c. Clin Genet. 2021 Jul;100(1):100-105. doi: 10.1111/cge.13963. Epub 2021 Apr 13. Clin Genet. 2021. PMID: 33822359
47 results