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2006 1
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2019 3
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28 results

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Page 1
Nusinersen versus Sham Control in Infantile-Onset Spinal Muscular Atrophy.
Finkel RS, Mercuri E, Darras BT, Connolly AM, Kuntz NL, Kirschner J, Chiriboga CA, Saito K, Servais L, Tizzano E, Topaloglu H, Tulinius M, Montes J, Glanzman AM, Bishop K, Zhong ZJ, Gheuens S, Bennett CF, Schneider E, Farwell W, De Vivo DC; ENDEAR Study Group. Finkel RS, et al. N Engl J Med. 2017 Nov 2;377(18):1723-1732. doi: 10.1056/NEJMoa1702752. N Engl J Med. 2017. PMID: 29091570 Free article. Clinical Trial.
Intrathecal onasemnogene abeparvovec for treatment-experienced patients with spinal muscular atrophy: a phase 3b, open-label trial.
Kwon JM, Munell F, Le Goff L, Yuge K, Kato T, Cances C, De Waele L, Woodcock IR, Mercuri EM, Proud CM, Darras BT, Hayes LH, Oskoui M, Visootsak J, Williams G, Ilić A, Yang L, van der Pol WL. Kwon JM, et al. Among authors: woodcock ir. Nat Med. 2026 Feb;32(2):488-493. doi: 10.1038/s41591-025-04119-2. Epub 2025 Dec 8. Nat Med. 2026. PMID: 41360995 Free PMC article. Clinical Trial.
Recessive MYH7-related myopathy in two families.
Beecroft SJ, van de Locht M, de Winter JM, Ottenheijm CA, Sewry CA, Mohammed S, Ryan MM, Woodcock IR, Sanders L, Gooding R, Davis MR, Oates EC, Laing NG, Ravenscroft G, McLean CA, Jungbluth H. Beecroft SJ, et al. Among authors: woodcock ir. Neuromuscul Disord. 2019 Jun;29(6):456-467. doi: 10.1016/j.nmd.2019.04.002. Epub 2019 Apr 12. Neuromuscul Disord. 2019. PMID: 31130376
Survival in Duchenne muscular dystrophy in Australia: a 50 year retrospective cohort study.
Davidson ZE, Vidmar S, Griffiths A, Howard ME, Berlowitz DJ, Jones EF, Scully T, Treanor D, Singh B, Prior D, Frost MG, Forbes R, Billich N, Adams J, Carroll K, Al Lawati T, Bourne H, Kornberg AJ, Ryan MM, Woodcock IR, Yiu EM, Cheung MMH. Davidson ZE, et al. Among authors: woodcock ir. Lancet Reg Health West Pac. 2025 May 8;58:101568. doi: 10.1016/j.lanwpc.2025.101568. eCollection 2025 May. Lancet Reg Health West Pac. 2025. PMID: 40470523 Free PMC article.
Nusinersen for SMA: expanded access programme.
Farrar MA, Teoh HL, Carey KA, Cairns A, Forbes R, Herbert K, Holland S, Jones KJ, Menezes MP, Morrison M, Munro K, Villano D, Webster R, Woodcock IR, Yiu EM, Sampaio H, Ryan MM. Farrar MA, et al. Among authors: woodcock ir. J Neurol Neurosurg Psychiatry. 2018 Sep;89(9):937-942. doi: 10.1136/jnnp-2017-317412. Epub 2018 Mar 16. J Neurol Neurosurg Psychiatry. 2018. PMID: 29549190
Effect of creatine monohydrate on motor function in children with facioscapulohumeral muscular dystrophy: A multicenter, randomized, double-blind placebo-controlled crossover trial.
Woodcock IR, de Valle K, Cairns A, Davidson ZE, Kean M, Varma N, Grobler A, Metz D, Carroll K, Dilek N, Heatwole C, Ryan MM, Delatycki MB, Yiu EM. Woodcock IR, et al. Pharmacotherapy. 2025 Jun;45(6):341-351. doi: 10.1002/phar.70025. Epub 2025 May 14. Pharmacotherapy. 2025. PMID: 40366059 Free PMC article. Clinical Trial.
Delivering multidisciplinary neuromuscular care for children via telehealth.
Carroll K, Adams J, de Valle K, Forbes R, Kennedy RA, Kornberg AJ, Vandeleur M, Villano D, Woodcock IR, Yiu EM, Ryan MM, Davidson Z. Carroll K, et al. Among authors: woodcock ir. Muscle Nerve. 2022 Jul;66(1):31-38. doi: 10.1002/mus.27557. Epub 2022 Apr 29. Muscle Nerve. 2022. PMID: 35426158 Free PMC article.
279th ENMC international workshop: Classification, clinical care, outcome measures and biomarkers in childhood onset facioscapulohumeral dystrophy: towards standardizing clinical care and ensuring clinical trial readiness. Hoofddorp, The Netherlands, 1-3 November 2024.
Dijkstra JN, Henzi BC, Mathews KD, Erasmus CE, Knox R, Willis T, de Valle K; ENMC 279th Workshop Study Group. Dijkstra JN, et al. Neuromuscul Disord. 2025 Oct;55:106236. doi: 10.1016/j.nmd.2025.106236. Epub 2025 Oct 1. Neuromuscul Disord. 2025. PMID: 41100957
28 results