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167 results

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Page 1
Eplontersen for Hereditary Transthyretin Amyloidosis With Polyneuropathy.
Coelho T, Marques W Jr, Dasgupta NR, Chao CC, Parman Y, França MC Jr, Guo YC, Wixner J, Ro LS, Calandra CR, Kowacs PA, Berk JL, Obici L, Barroso FA, Weiler M, Conceição I, Jung SW, Buchele G, Brambatti M, Chen J, Hughes SG, Schneider E, Viney NJ, Masri A, Gertz MR, Ando Y, Gillmore JD, Khella S, Dyck PJB, Waddington Cruz M; NEURO-TTRansform Investigators. Coelho T, et al. Among authors: ro ls. JAMA. 2023 Oct 17;330(15):1448-1458. doi: 10.1001/jama.2023.18688. JAMA. 2023. PMID: 37768671 Free PMC article.
Biomarkers for neuromyelitis optica.
Chang KH, Ro LS, Lyu RK, Chen CM. Chang KH, et al. Among authors: ro ls. Clin Chim Acta. 2015 Feb 2;440:64-71. doi: 10.1016/j.cca.2014.11.004. Epub 2014 Nov 7. Clin Chim Acta. 2015. PMID: 25444748 Review.
The benefits and challenges of family genetic testing in rare genetic diseases-lessons from Fabry disease.
Germain DP, Moiseev S, Suárez-Obando F, Al Ismaili F, Al Khawaja H, Altarescu G, Barreto FC, Haddoum F, Hadipour F, Maksimova I, Kramis M, Nampoothiri S, Nguyen KN, Niu DM, Politei J, Ro LS, Vu Chi D, Chen N, Kutsev S. Germain DP, et al. Among authors: ro ls. Mol Genet Genomic Med. 2021 May;9(5):e1666. doi: 10.1002/mgg3.1666. Epub 2021 Apr 9. Mol Genet Genomic Med. 2021. PMID: 33835733 Free PMC article. Review.
Electrophysiological features of Hirayama disease.
Lyu RK, Huang YC, Wu YR, Kuo HC, Ro LS, Chen CM, Chang HS. Lyu RK, et al. Among authors: ro ls. Muscle Nerve. 2011 Aug;44(2):185-90. doi: 10.1002/mus.22028. Muscle Nerve. 2011. PMID: 21755506
Painful ophthalmoplegia with normal cranial imaging.
Hung CH, Chang KH, Chu CC, Liao MF, Chang HS, Lyu RK, Wu YM, Chen YL, Lai CL, Tseng HJ, Ro LS. Hung CH, et al. Among authors: ro ls. BMC Neurol. 2014 Jan 9;14:7. doi: 10.1186/1471-2377-14-7. BMC Neurol. 2014. PMID: 24400984 Free PMC article.
167 results