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A novel case of inclusion body myositis and myasthenia gravis.
Lambrianides S, Kinnis E, Cleanthous M, Papacharalambous R, Panayiotou E, Zamba-Papanicolaou E, Kyriakides T. Lambrianides S, et al. Neuromuscul Disord. 2019 Oct;29(10):771-775. doi: 10.1016/j.nmd.2019.09.004. Epub 2019 Sep 6. Neuromuscul Disord. 2019. PMID: 31604651
Long-term safety and efficacy of patisiran for hereditary transthyretin-mediated amyloidosis with polyneuropathy: 12-month results of an open-label extension study.
Adams D, Polydefkis M, González-Duarte A, Wixner J, Kristen AV, Schmidt HH, Berk JL, Losada López IA, Dispenzieri A, Quan D, Conceição IM, Slama MS, Gillmore JD, Kyriakides T, Ajroud-Driss S, Waddington-Cruz M, Mezei MM, Planté-Bordeneuve V, Attarian S, Mauricio E, Brannagan TH 3rd, Ueda M, Aldinc E, Wang JJ, White MT, Vest J, Berber E, Sweetser MT, Coelho T; patisiran Global OLE study group. Adams D, et al. Lancet Neurol. 2021 Jan;20(1):49-59. doi: 10.1016/S1474-4422(20)30368-9. Epub 2020 Nov 16. Lancet Neurol. 2021. PMID: 33212063 Clinical Trial.
Parkes Weber syndrome: a rare cause of foot drop.
Kyriakides DE, Michaelides D, Lambrianides S. Kyriakides DE, et al. Among authors: lambrianides s. BMJ Case Rep. 2023 Oct 4;16(10):e254455. doi: 10.1136/bcr-2022-254455. BMJ Case Rep. 2023. PMID: 37793841