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

Year Number of Results
1973 1
1989 1
1991 1
1995 2
1997 2
1998 2
1999 5
2001 3
2002 2
2003 9
2004 5
2005 5
2006 5
2007 7
2008 2
2009 3
2010 5
2011 3
2012 5
2013 4
2014 4
2015 7
2016 8
2017 9
2018 6
2019 9
2020 11
2021 10
2022 10
2023 9
2024 9

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143 results

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Page 1
European consensus statement on phenotypes of pustular psoriasis.
Navarini AA, Burden AD, Capon F, Mrowietz U, Puig L, Köks S, Kingo K, Smith C, Barker JN; ERASPEN Network. Navarini AA, et al. J Eur Acad Dermatol Venereol. 2017 Nov;31(11):1792-1799. doi: 10.1111/jdv.14386. Epub 2017 Aug 29. J Eur Acad Dermatol Venereol. 2017. PMID: 28585342 Free article. Review.
Rosacea fulminans.
Koh HY, Ng SK, Tan WP. Koh HY, et al. Indian J Dermatol Venereol Leprol. 2014 May-Jun;80(3):272-4. doi: 10.4103/0378-6323.132267. Indian J Dermatol Venereol Leprol. 2014. PMID: 24823417 Free article. No abstract available.
Genotypes and phenotypes of DNM1 encephalopathy.
Kim J, Teng LY, Shaker B, Na D, Koh HY, Kwon SS, Lee JS, Kim HD, Kang HC, Kim SH. Kim J, et al. Among authors: koh hy. J Med Genet. 2023 Nov;60(11):1076-1083. doi: 10.1136/jmg-2023-109233. Epub 2023 May 29. J Med Genet. 2023. PMID: 37248033
Brain Somatic Mutations in Epileptic Disorders.
Koh HY, Lee JH. Koh HY, et al. Mol Cells. 2018 Oct 31;41(10):881-888. doi: 10.14348/molcells.2018.0247. Epub 2018 Oct 10. Mol Cells. 2018. PMID: 30352490 Free PMC article. Review.
Utility of Exome Sequencing for Diagnosis in Unexplained Pediatric-Onset Epilepsy.
Koh HY, Smith L, Wiltrout KN, Podury A, Chourasia N, D'Gama AM, Park M, Knight D, Sexton EL, Koh JJ, Oby B, Pinsky R, Shao DD, French CE, Shao W, Rockowitz S, Sliz P, Zhang B, Mahida S, Moufawad El Achkar C, Yuskaitis CJ, Olson HE, Sheidley BR, Poduri AH; BCH Neurology Referral and Phenotyping Group. Koh HY, et al. JAMA Netw Open. 2023 Jul 3;6(7):e2324380. doi: 10.1001/jamanetworkopen.2023.24380. JAMA Netw Open. 2023. PMID: 37471090 Free PMC article.
Somatic variants in diverse genes leads to a spectrum of focal cortical malformations.
Lai D, Gade M, Yang E, Koh HY, Lu J, Walley NM, Buckley AF, Sands TT, Akman CI, Mikati MA, McKhann GM, Goldman JE, Canoll P, Alexander AL, Park KL, Von Allmen GK, Rodziyevska O, Bhattacharjee MB, Lidov HGW, Vogel H, Grant GA, Porter BE, Poduri AH, Crino PB, Heinzen EL. Lai D, et al. Among authors: koh hy. Brain. 2022 Aug 27;145(8):2704-2720. doi: 10.1093/brain/awac117. Brain. 2022. PMID: 35441233 Free PMC article.
143 results