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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.
Epidemiological and genetic studies of myotonic dystrophy type 1 in Taiwan.
Hsiao KM, Chen SS, Li SY, Chiang SY, Lin HM, Pan H, Huang CC, Kuo HC, Jou SB, Su CC, Ro LS, Liu CS, Lo MC, Chen CM, Lin CC. Hsiao KM, et al. Among authors: ro ls. Neuroepidemiology. 2003 Sep-Oct;22(5):283-9. doi: 10.1159/000071191. Neuroepidemiology. 2003. PMID: 12902623
Long-term follow-up of spinal and bulbar muscular atrophy in Taiwan.
Fu SC, Kuo HC, Chu CC, Wu YR, Ro LS, Liu CS, Huang CC. Fu SC, et al. Among authors: ro ls. J Formos Med Assoc. 2013 Jun;112(6):326-31. doi: 10.1016/j.jfma.2012.03.008. Epub 2012 Jun 6. J Formos Med Assoc. 2013. PMID: 23787009 Free article.
165 results