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A novel homozygous PLA2G6 mutation causes dystonia-parkinsonism.
Malaguti MC, Melzi V, Di Giacopo R, Monfrini E, Di Biase E, Franco G, Borellini L, Trezzi I, Monzio Compagnoni G, Fortis P, Feraco P, Orrico D, Cucurachi L, Donner D, Rizzuti M, Ronchi D, Bonato S, Bresolin N, Corti S, Comi GP, Di Fonzo A. Malaguti MC, et al. Among authors: comi gp. Parkinsonism Relat Disord. 2015 Mar;21(3):337-9. doi: 10.1016/j.parkreldis.2015.01.001. Epub 2015 Jan 10. Parkinsonism Relat Disord. 2015. PMID: 25601130 No abstract available.
Cognitive impairment in Duchenne muscular dystrophy.
Bresolin N, Castelli E, Comi GP, Felisari G, Bardoni A, Perani D, Grassi F, Turconi A, Mazzucchelli F, Gallotti D, et al. Bresolin N, et al. Among authors: comi gp. Neuromuscul Disord. 1994 Jul;4(4):359-69. doi: 10.1016/0960-8966(94)90072-8. Neuromuscul Disord. 1994. PMID: 7981593
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.
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: comi gp. 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.
514 results