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TARDBP mutations in frontotemporal lobar degeneration: frequency, clinical features, and disease course.
Rejuvenation Res. 2010 Oct;13(5):509-17. doi: 10.1089/rej.2010.1017. Epub 2010 Jul 20.
Rejuvenation Res. 2010.
PMID: 20645878
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. Among authors: pietro comi g.
Neurobiol Aging. 2003 Oct;24(6):829-38. doi: 10.1016/s0197-4580(02)00233-6.
Neurobiol Aging. 2003.
PMID: 12927765
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Skeletal muscle differentiation potential of human adult bone marrow cells.
Bossolasco P, Corti S, Strazzer S, Borsotti C, Del Bo R, Fortunato F, Salani S, Quirici N, Bertolini F, Gobbi A, Deliliers GL, Pietro Comi G, Soligo D.
Bossolasco P, et al. Among authors: pietro comi g.
Exp Cell Res. 2004 Apr 15;295(1):66-78. doi: 10.1016/j.yexcr.2003.12.015.
Exp Cell Res. 2004.
PMID: 15051491
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Reply: DGUOK recessive mutations in patients with CPEO, mitochondrial myopathy, parkinsonism and mtDNA deletions.
Ronchi D, Piga D, Lamberti S, Sciacco M, Corti S, Moggio M, Bresolin N, Pietro Comi G.
Ronchi D, et al. Among authors: pietro comi g.
Brain. 2018 Jan 1;141(1):e4. doi: 10.1093/brain/awx302.
Brain. 2018.
PMID: 29228135
Free article.
No abstract available.
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Diagnostic and prognostic value of CSF neurofilaments in a cohort of patients with motor neuron disease: A cross-sectional study.
Gagliardi D, Faravelli I, Meneri M, Saccomanno D, Govoni A, Magri F, Ricci G, Siciliano G, Pietro Comi G, Corti S.
Gagliardi D, et al. Among authors: pietro comi g.
J Cell Mol Med. 2021 Apr;25(8):3765-3771. doi: 10.1111/jcmm.16240. Epub 2021 Feb 20.
J Cell Mol Med. 2021.
PMID: 33609080
Free PMC article.
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