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Year Number of Results
1994 1
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1998 3
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2002 2
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2004 8
2005 8
2006 10
2007 8
2008 9
2009 6
2010 5
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163 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.
Safety, tolerability, and efficacy of subcutaneous efgartigimod in patients with chronic inflammatory demyelinating polyradiculoneuropathy (ADHERE): a multicentre, randomised-withdrawal, double-blind, placebo-controlled, phase 2 trial.
Allen JA, Lin J, Basta I, Dysgaard T, Eggers C, Guptill JT, Gwathmey KG, Hewamadduma C, Hofman E, Hussain YM, Kuwabara S, Le Masson G, Leypoldt F, Chang T, Lipowska M, Lowe M, Lauria G, Querol L, Simu MA, Suresh N, Tse A, Ulrichts P, Van Hoorick B, Yamasaki R, Lewis RA, van Doorn PA; ADHERE Study Group. Allen JA, et al. Lancet Neurol. 2024 Oct;23(10):1013-1024. doi: 10.1016/S1474-4422(24)00309-0. Lancet Neurol. 2024. PMID: 39304241 Clinical Trial.
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.
Hirayama disease: MR diagnosis.
Chen CJ, Chen CM, Wu CL, Ro LS, Chen ST, Lee TH. Chen CJ, et al. Among authors: ro ls. AJNR Am J Neuroradiol. 1998 Feb;19(2):365-8. AJNR Am J Neuroradiol. 1998. PMID: 9504496 Free PMC article.
Balò's concentric sclerosis: MRI.
Chen CJ, Ro LS, Wang LJ, Wong YC. Chen CJ, et al. Among authors: ro ls. Neuroradiology. 1996 May;38(4):322-4. doi: 10.1007/BF00596578. Neuroradiology. 1996. PMID: 8738087
163 results