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1992 1
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480 results

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Page 1
A defect in mitochondrial fatty acid synthesis impairs iron metabolism and causes elevated ceramide levels.
Dutta D, Kanca O, Byeon SK, Marcogliese PC, Zuo Z, Shridharan RV, Park JH; Undiagnosed Diseases Network; Lin G, Ge M, Heimer G, Kohler JN, Wheeler MT, Kaipparettu BA, Pandey A, Bellen HJ. Dutta D, et al. Among authors: byeon sk. Nat Metab. 2023 Sep;5(9):1595-1614. doi: 10.1038/s42255-023-00873-0. Epub 2023 Aug 31. Nat Metab. 2023. PMID: 37653044 Free PMC article.
Development of a multiomics model for identification of predictive biomarkers for COVID-19 severity: a retrospective cohort study.
Byeon SK, Madugundu AK, Garapati K, Ramarajan MG, Saraswat M, Kumar-M P, Hughes T, Shah R, Patnaik MM, Chia N, Ashrafzadeh-Kian S, Yao JD, Pritt BS, Cattaneo R, Salama ME, Zenka RM, Kipp BR, Grebe SKG, Singh RJ, Sadighi Akha AA, Algeciras-Schimnich A, Dasari S, Olson JE, Walsh JR, Venkatakrishnan AJ, Jenkinson G, O'Horo JC, Badley AD, Pandey A. Byeon SK, et al. Lancet Digit Health. 2022 Sep;4(9):e632-e645. doi: 10.1016/S2589-7500(22)00112-1. Epub 2022 Jul 11. Lancet Digit Health. 2022. PMID: 35835712 Free PMC article.
Pharmacokinetics.
Byeon SH, Kang SY. Byeon SH, et al. Ophthalmology. 2009 Jan;116(1):168-9; author reply 169-70. doi: 10.1016/j.ophtha.2008.09.016. Ophthalmology. 2009. PMID: 19118710 No abstract available.
Reply.
Lee DH, Han JW, Kim SS, Byeon SH, Koh HJ, Lee SC, Kim M. Lee DH, et al. Among authors: byeon sh. Am J Ophthalmol. 2018 Sep;193:252-253. doi: 10.1016/j.ajo.2018.06.014. Epub 2018 Jul 23. Am J Ophthalmol. 2018. PMID: 30049479 No abstract available.
Dome-shaped macula.
Byeon SH, Chu YK. Byeon SH, et al. Am J Ophthalmol. 2011 Jun;151(6):1101; author reply 1101-2. doi: 10.1016/j.ajo.2011.01.054. Am J Ophthalmol. 2011. PMID: 21616212 No abstract available.
Retinal Hemorrhage after SARS-CoV-2 Vaccination.
Park HS, Byun Y, Byeon SH, Kim SS, Kim YJ, Lee CS. Park HS, et al. Among authors: byeon sh. J Clin Med. 2021 Dec 5;10(23):5705. doi: 10.3390/jcm10235705. J Clin Med. 2021. PMID: 34884407 Free PMC article.
TRIT1 defect leads to a recognizable phenotype of myoclonic epilepsy, speech delay, strabismus, progressive spasticity, and normal lactate levels.
Muylle E, Jiang H, Johnsen C, Byeon SK, Ranatunga W, Garapati K, Zenka RM, Preston G, Pandey A, Kozicz T, Fang F, Morava E. Muylle E, et al. Among authors: byeon sk. J Inherit Metab Dis. 2022 Nov;45(6):1039-1047. doi: 10.1002/jimd.12550. Epub 2022 Sep 21. J Inherit Metab Dis. 2022. PMID: 36047296 Free PMC article. Review.
480 results