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

Year Number of Results
1986 1
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2001 3
2002 4
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2005 5
2006 5
2007 6
2008 6
2009 7
2010 6
2011 6
2012 8
2013 10
2014 5
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2022 4
2023 8
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124 results

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Page 1
Correspondence.
Chen N, Hsiao MC, Wang NK. Chen N, et al. Among authors: hsiao mc. Retina. 2023 Feb 1;43(2):e9-e11. doi: 10.1097/IAE.0000000000003664. Retina. 2023. PMID: 36695807 Free PMC article. No abstract available.
Investigation into the genetics of fetal congenital lymphatic anomalies.
Rogerson D, Alkelai A, Giordano J, Pantrangi M, Hsiao MC, Nhan-Chang CL, Motelow JE, Aggarwal V, Goldstein D, Wapner R, Shawber CJ. Rogerson D, et al. Among authors: hsiao mc. Prenat Diagn. 2023 Jun;43(6):703-716. doi: 10.1002/pd.6345. Epub 2023 Apr 3. Prenat Diagn. 2023. PMID: 36959127 Free PMC article.
Decoding NF1 Intragenic Copy-Number Variations.
Hsiao MC, Piotrowski A, Callens T, Fu C, Wimmer K, Claes KB, Messiaen L. Hsiao MC, et al. Am J Hum Genet. 2015 Aug 6;97(2):238-49. doi: 10.1016/j.ajhg.2015.06.002. Epub 2015 Jul 16. Am J Hum Genet. 2015. PMID: 26189818 Free PMC article.
Taiwan consensus of pharmacological treatment for bipolar disorder.
Bai YM, Chang CJ, Tsai SY, Chen YC, Hsiao MC, Li CT, Tu P, Chang SW, Shen WW, Su TP. Bai YM, et al. Among authors: hsiao mc. J Chin Med Assoc. 2013 Oct;76(10):547-56. doi: 10.1016/j.jcma.2013.06.013. Epub 2013 Aug 8. J Chin Med Assoc. 2013. PMID: 23933343 Free article. Review.
Congenital Stationary Night Blindness: Clinical and Genetic Features.
Kim AH, Liu PK, Chang YH, Kang EY, Wang HH, Chen N, Tseng YJ, Seo GH, Lee H, Liu L, Chao AN, Chen KJ, Hwang YS, Wu WC, Lai CC, Tsang SH, Hsiao MC, Wang NK. Kim AH, et al. Among authors: hsiao mc. Int J Mol Sci. 2022 Nov 29;23(23):14965. doi: 10.3390/ijms232314965. Int J Mol Sci. 2022. PMID: 36499293 Free PMC article.
Unusual manifestations of premenstrual syndrome.
Hsiao MC, Liu CY. Hsiao MC, et al. Psychiatry Clin Neurosci. 2007 Feb;61(1):120-3. doi: 10.1111/j.1440-1819.2007.01620.x. Psychiatry Clin Neurosci. 2007. PMID: 17239049 Free article.
Maternal Mosaicism in SSBP1 Causing Optic Atrophy with Retinal Degeneration: Implications for Genetic Counseling.
Chang YH, Kang EY, Liu L, Jenny LA, Khang R, Seo GH, Lee H, Chen KJ, Wu WC, Hsiao MC, Wang NK. Chang YH, et al. Among authors: hsiao mc. Res Sq [Preprint]. 2023 Mar 15:rs.3.rs-2554402. doi: 10.21203/rs.3.rs-2554402/v1. Res Sq. 2023. Update in: Orphanet J Rare Dis. 2023 May 31;18(1):131. doi: 10.1186/s13023-023-02748-9. PMID: 36993412 Free PMC article. Updated. Preprint.
124 results