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Down's syndrome fibroblasts anticipate the accumulation of specific ageing-related mtDNA mutations.
Del Bo R, Comi GP, Perini MP, Strazzer S, Bresolin N, Scarlato G. Del Bo R, et al. Ann Neurol. 2001 Jan;49(1):137-8. doi: 10.1002/1531-8249(200101)49:1<137::aid-ana26>;2-i. Ann Neurol. 2001. PMID: 11198288 No abstract available.
Evidence and age-related distribution of mtDNA D-loop point mutations in skeletal muscle from healthy subjects and mitochondrial patients.
Del Bo R, Bordoni A, Martinelli Boneschi F, Crimi M, Sciacco M, Bresolin N, Scarlato G, Comi GP. Del Bo R, et al. J Neurol Sci. 2002 Oct 15;202(1-2):85-91. doi: 10.1016/s0022-510x(02)00247-2. J Neurol Sci. 2002. PMID: 12220698
A collection of 33 novel human mtDNA homoplasmic variants.
Crimi M, Sciacco M, Galbiati S, Bordoni A, Malferrari G, Del Bo R, Biunno I, Bresolin N, Comi GP. Crimi M, et al. Hum Mutat. 2002 Nov;20(5):409. doi: 10.1002/humu.9079. Hum Mutat. 2002. PMID: 12402350
Modulated generation of neuronal cells from bone marrow by expansion and mobilization of circulating stem cells with in vivo cytokine treatment.
Corti S, Locatelli F, Strazzer S, Salani S, Del Bo R, Soligo D, Bossolasco P, Bresolin N, Scarlato G, Comi GP. Corti S, et al. Exp Neurol. 2002 Oct;177(2):443-52. doi: 10.1006/exnr.2002.8004. Exp Neurol. 2002. PMID: 12429190
The 129 codon polymorphism of the prion protein gene influences earlier cognitive performance in Down syndrome subjects.
Del Bo R, Comi GP, Giorda R, Crimi M, Locatelli F, Martinelli-Boneschi F, Pozzoli U, Castelli E, Bresolin N, Scarlato G. Del Bo R, et al. J Neurol. 2003 Jun;250(6):688-92. doi: 10.1007/s00415-003-1057-5. J Neurol. 2003. PMID: 12796830
High mutational burden in the mtDNA control region from aged muscles: a single-fiber study.
Del Bo R, Crimi M, Sciacco M, Malferrari G, Bordoni A, Napoli L, Prelle A, Biunno I, Moggio M, Bresolin N, Scarlato G, Pietro Comi G. Del Bo R, et al. Neurobiol Aging. 2003 Oct;24(6):829-38. doi: 10.1016/s0197-4580(02)00233-6. Neurobiol Aging. 2003. PMID: 12927765
POLG mutations in sporadic mitochondrial disorders with multiple mtDNA deletions.
Di Fonzo A, Bordoni A, Crimi M, Sara G, Del Bo R, Bresolin N, Comi GP. Di Fonzo A, et al. Hum Mutat. 2003 Dec;22(6):498-9. doi: 10.1002/humu.9203. Hum Mutat. 2003. PMID: 14635118
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