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

Year Number of Results
1963 2
1964 1
1966 1
1967 1
1969 1
1970 1
1973 2
1978 1
1979 3
1981 4
1982 1
1983 2
1984 1
1985 1
1986 2
1987 1
1988 2
1989 3
1990 4
1991 4
1992 8
1993 3
1994 2
1995 3
1996 4
1997 1
1999 1
2000 1
2001 1
2002 1
2003 2
2004 3
2005 7
2006 8
2007 7
2008 13
2009 10
2010 8
2011 5
2012 5
2013 6
2014 12
2015 17
2016 15
2017 11
2018 15
2019 17
2020 18
2021 17
2022 30
2023 19
2024 8

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277 results

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Page 1
Nanoparticles' interactions with vasculature in diseases.
Tee JK , Yip LX , Tan ES , Santitewagun S , Prasath A , Ke PC , Ho HK , Leong DT . Tee JK , et al. Among authors: tan es. Chem Soc Rev. 2019 Oct 28;48(21):5381-5407. doi: 10.1039/c9cs00309f. Chem Soc Rev. 2019. PMID: 31495856 Review.
Nail psoriasis: a review.
Tan ES, Chong WS, Tey HL. Tan ES, et al. Am J Clin Dermatol. 2012 Dec 1;13(6):375-88. doi: 10.2165/11597000-000000000-00000. Am J Clin Dermatol. 2012. PMID: 22784035 Review.
The diabetes-atrial fibrillation paradox.
Tan ESJ, Tay WT, Teng TK, Richards AM, Doughty RN, Lam CSP. Tan ESJ, et al. Heart. 2019 Jun;105(11):893. doi: 10.1136/heartjnl-2019-315018. Heart. 2019. PMID: 31092681 No abstract available.
Hemiplegia and rehabilitation.
Tan ES. Tan ES. Nurs J Singapore. 1983 Oct-Nov;23:46-7. Nurs J Singapore. 1983. PMID: 6560405 No abstract available.
Inactivation of DRG1, encoding a translation factor GTPase, causes a recessive neurodevelopmental disorder.
Westrip CAE, Paul F, Al-Murshedi F, Qaitoon H, Cham B, Fletcher SC, Hendrix E, Boora U, Ng AYJ, Bonnard C, Najafi M, Alawbathani S, Lambert I, Fox G, Venkatesh B, Bertoli-Avella A, Tan ES, Al-Maawali A, Reversade B, Coleman ML. Westrip CAE, et al. Among authors: tan es. Genet Med. 2023 Sep;25(9):100893. doi: 10.1016/j.gim.2023.100893. Epub 2023 May 11. Genet Med. 2023. PMID: 37179472 Free article.
Williams-Beuren syndrome in diverse populations.
Kruszka P, Porras AR, de Souza DH, Moresco A, Huckstadt V, Gill AD, Boyle AP, Hu T, Addissie YA, Mok GTK, Tekendo-Ngongang C, Fieggen K, Prijoles EJ, Tanpaiboon P, Honey E, Luk HM, Lo IFM, Thong MK, Muthukumarasamy P, Jones KL, Belhassan K, Ouldim K, El Bouchikhi I, Bouguenouch L, Shukla A, Girisha KM, Sirisena ND, Dissanayake VHW, Paththinige CS, Mishra R, Kisling MS, Ferreira CR, de Herreros MB, Lee NC, Jamuar SS, Lai A, Tan ES, Ying Lim J, Wen-Min CB, Gupta N, Lotz-Esquivel S, Badilla-Porras R, Hussen DF, El Ruby MO, Ashaat EA, Patil SJ, Dowsett L, Eaton A, Innes AM, Shotelersuk V, Badoe Ë, Wonkam A, Obregon MG, Chung BHY, Trubnykova M, La Serna J, Gallardo Jugo BE, Chávez Pastor M, Abarca Barriga HH, Megarbane A, Kozel BA, van Haelst MM, Stevenson RE, Summar M, Adeyemo AA, Morris CA, Moretti-Ferreira D, Linguraru MG, Muenke M. Kruszka P, et al. Among authors: tan es. Am J Med Genet A. 2018 May;176(5):1128-1136. doi: 10.1002/ajmg.a.38672. Am J Med Genet A. 2018. PMID: 29681090 Free PMC article.
Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome.
Cousin MA, Veale EL, Dsouza NR, Tripathi S, Holden RG, Arelin M, Beek G, Bekheirnia MR, Beygo J, Bhambhani V, Bialer M, Bigoni S, Boelman C, Carmichael J, Courtin T, Cogne B, Dabaj I, Doummar D, Fazilleau L, Ferlini A, Gavrilova RH, Graham JM Jr, Haack TB, Juusola J, Kant SG, Kayani S, Keren B, Ketteler P, Klöckner C, Koopmann TT, Kruisselbrink TM, Kuechler A, Lambert L, Latypova X, Lebel RR, Leduc MS, Leonardi E, Lewis AM, Liew W, Machol K, Mardini S, McWalter K, Mignot C, McLaughlin J, Murgia A, Narayanan V, Nava C, Neuser S, Nizon M, Ognibene D, Park J, Platzer K, Poirsier C, Radtke M, Ramsey K, Runke CK, Guillen Sacoto MJ, Scaglia F, Shinawi M, Spranger S, Tan ES, Taylor J, Trentesaux AS, Vairo F, Willaert R, Zadeh N, Urrutia R, Babovic-Vuksanovic D, Zimmermann MT, Mathie A, Klee EW. Cousin MA, et al. Among authors: tan es. Genome Med. 2022 Jun 13;14(1):62. doi: 10.1186/s13073-022-01064-4. Genome Med. 2022. PMID: 35698242 Free PMC article.
277 results