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514 results

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Page 1
Ataluren treatment of patients with nonsense mutation dystrophinopathy.
Bushby K, Finkel R, Wong B, Barohn R, Campbell C, Comi GP, Connolly AM, Day JW, Flanigan KM, Goemans N, Jones KJ, Mercuri E, Quinlivan R, Renfroe JB, Russman B, Ryan MM, Tulinius M, Voit T, Moore SA, Lee Sweeney H, Abresch RT, Coleman KL, Eagle M, Florence J, Gappmaier E, Glanzman AM, Henricson E, Barth J, Elfring GL, Reha A, Spiegel RJ, O'donnell MW, Peltz SW, Mcdonald CM; PTC124-GD-007-DMD STUDY GROUP. Bushby K, et al. Among authors: comi gp. Muscle Nerve. 2014 Oct;50(4):477-87. doi: 10.1002/mus.24332. Muscle Nerve. 2014. PMID: 25042182 Free PMC article. Clinical Trial.
In vivo biolistic technique in control and mdx dystrophic mice.
Ausenda CD, Bresolin N, De Liso A, D'Angelo MG, Moggio M, Del Bo R, Gallanti A, Comi GP, Torrente Y, Bordoni A, Scarlato G. Ausenda CD, et al. Among authors: comi gp. Muscle Nerve. 1996 Jul;19(7):912-4. doi: 10.1002/(SICI)1097-4598(199607)19:7<912::AID-MUS18>3.0.CO;2-K. Muscle Nerve. 1996. PMID: 8965850 No abstract available.
Intra-aortic injection of myoblasts in mdx mice: genetic and technetium-99m cell labeling and biodistribution.
Bresolin N, Ausenda CD, Casati R, Torrente Y, DeLiso A, D'Angelo MG, Benti R, Moggio M, Baldessari S, Comi GP, Colombo F, Gerundini P, Scarlato G. Bresolin N, et al. Among authors: comi gp. Muscle Nerve. 1997 Jun;20(6):757-9. doi: 10.1002/(sici)1097-4598(199706)20:6<757::aid-mus17>3.0.co;2-r. Muscle Nerve. 1997. PMID: 9149087 No abstract available.
Genotype and phenotype characterization in a large dystrophinopathic cohort with extended follow-up.
Magri F, Govoni A, D'Angelo MG, Del Bo R, Ghezzi S, Sandra G, Turconi AC, Sciacco M, Ciscato P, Bordoni A, Tedeschi S, Fortunato F, Lucchini V, Bonato S, Lamperti C, Coviello D, Torrente Y, Corti S, Moggio M, Bresolin N, Comi GP. Magri F, et al. Among authors: comi gp. J Neurol. 2011 Sep;258(9):1610-23. doi: 10.1007/s00415-011-5979-z. Epub 2011 Mar 12. J Neurol. 2011. PMID: 21399986
Neurocognitive profiles in Duchenne muscular dystrophy and gene mutation site.
D'Angelo MG, Lorusso ML, Civati F, Comi GP, Magri F, Del Bo R, Guglieri M, Molteni M, Turconi AC, Bresolin N. D'Angelo MG, et al. Among authors: comi gp. Pediatr Neurol. 2011 Nov;45(5):292-9. doi: 10.1016/j.pediatrneurol.2011.08.003. Pediatr Neurol. 2011. PMID: 22000308 Free PMC article.
Frequency and characterisation of anoctamin 5 mutations in a cohort of Italian limb-girdle muscular dystrophy patients.
Magri F, Del Bo R, D'Angelo MG, Sciacco M, Gandossini S, Govoni A, Napoli L, Ciscato P, Fortunato F, Brighina E, Bonato S, Bordoni A, Lucchini V, Corti S, Moggio M, Bresolin N, Comi GP. Magri F, et al. Among authors: comi gp. Neuromuscul Disord. 2012 Nov;22(11):934-43. doi: 10.1016/j.nmd.2012.05.001. Epub 2012 Jun 27. Neuromuscul Disord. 2012. PMID: 22742934 Free PMC article.
514 results