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No major progranulin genetic variability contribution to disease etiopathogenesis in an ALS Italian cohort.
Del Bo R, Corti S, Santoro D, Ghione I, Fenoglio C, Ghezzi S, Ranieri M, Galimberti D, Mancuso M, Siciliano G, Briani C, Murri L, Scarpini E, Schymick JC, Traynor BJ, Bresolin N, Comi GP. Del Bo R, et al. Among authors: bresolin n. Neurobiol Aging. 2011 Jun;32(6):1157-8. doi: 10.1016/j.neurobiolaging.2009.06.006. Epub 2009 Jul 25. Neurobiol Aging. 2011. PMID: 19632744 Free PMC article.
A G+1-->A transversion at the 5' splice site of intron 69 of the dystrophin gene causing the absence of peripheral nerve Dp116 and severe clinical involvement in a DMD patient.
Comi GP, Ciafaloni E, de Silva HA, Prelle A, Bardoni A, Rigoletto C, Robotti M, Bresolin N, Moggio M, Fortunato F. Comi GP, et al. Among authors: bresolin n. Hum Mol Genet. 1995 Nov;4(11):2171-4. doi: 10.1093/hmg/4.11.2171. Hum Mol Genet. 1995. PMID: 8589698 No abstract available.
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: bresolin n. 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.
Novel donor splice site mutations of AGL gene in glycogen storage disease type IIIa.
Hadjigeorgiou GM, Comi GP, Bordoni A, Shen J, Chen YT, Salani S, Toscano A, Fortunato F, Lucchiari S, Bresolin N, Rodolico C, Piscaglia MG, Franceschina L, Papadimitriou A, Scarlato G. Hadjigeorgiou GM, et al. Among authors: bresolin n. J Inherit Metab Dis. 1999 Aug;22(6):762-3. doi: 10.1023/a:1005572906807. J Inherit Metab Dis. 1999. PMID: 10472540 No abstract available.
593 results