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Systemic administration of PRO051 in Duchenne's muscular dystrophy.
Goemans NM, Tulinius M, van den Akker JT, Burm BE, Ekhart PF, Heuvelmans N, Holling T, Janson AA, Platenburg GJ, Sipkens JA, Sitsen JM, Aartsma-Rus A, van Ommen GJ, Buyse G, Darin N, Verschuuren JJ, Campion GV, de Kimpe SJ, van Deutekom JC. Goemans NM, et al. Among authors: tulinius m. N Engl J Med. 2011 Apr 21;364(16):1513-22. doi: 10.1056/NEJMoa1011367. Epub 2011 Mar 23. N Engl J Med. 2011. PMID: 21428760 Free article. Clinical Trial.
Mitochondrial myopathy and cardiomyopathy in siblings.
Tulinius MH, Eriksson BO, Hjalmarson O, Holme E, Oldfors A. Tulinius MH, et al. Pediatr Neurol. 1989 May-Jun;5(3):182-8. doi: 10.1016/0887-8994(89)90069-6. Pediatr Neurol. 1989. PMID: 2742628
Early-onset myopathy with tubular aggregates.
Tulinius MH, Lundberg A, Oldfors A. Tulinius MH, et al. Pediatr Neurol. 1996 Jul;15(1):68-71. doi: 10.1016/0887-8994(96)00094-x. Pediatr Neurol. 1996. PMID: 8858706 Review.
Meta-analyses of deflazacort versus prednisone/prednisolone in patients with nonsense mutation Duchenne muscular dystrophy.
Shieh PB, Elfring G, Trifillis P, Santos C, Peltz SW, Parsons JA, Apkon S, Darras BT, Campbell C, McDonald CM; Members of the Ataluren Phase IIb Study Group; Members of the Ataluren Phase IIb Study Clinical Evaluator Training Group; Members of the ACT DMD Study Group; Members of the ACT DMD Clinical Evaluator Training Group. Shieh PB, et al. J Comp Eff Res. 2021 Dec;10(18):1337-1347. doi: 10.2217/cer-2021-0018. Epub 2021 Oct 25. J Comp Eff Res. 2021. PMID: 34693725 Free article.
149 results