Checcarelli N - Search Results

1

Multiple sclerosis and mitochondrial myopathy: an unusual combination of diseases.

Bet L, Moggio M, Comi GP, Mariani C, Prelle A, Checcarelli N, Bordoni A, Bresolin N, Scarpini E, Scarlato G. Bet L, et al. Among authors: checcarelli n. J Neurol. 1994 Jul;241(8):511-6. doi: 10.1007/BF00919714. J Neurol. 1994. PMID: 7964921

2

Mitochondrial myopathy: correlation between oxidative defect and mitochondrial DNA deletions at single fiber level.

Prelle A, Fagiolari G, Checcarelli N, Moggio M, Battistel A, Comi GP, Bazzi P, Bordoni A, Zeviani M, Scarlato G. Prelle A, et al. Among authors: checcarelli n. Acta Neuropathol. 1994;87(4):371-6. doi: 10.1007/BF00313606. Acta Neuropathol. 1994. PMID: 8017172

3

Multiple deletions of mitochondrial DNA in sporadic and atypical cases of encephalomyopathy.

Checcarelli N, Prelle A, Moggio M, Comi G, Bresolin N, Papadimitriou A, Fagiolari G, Bordoni A, Scarlato G. Checcarelli N, et al. J Neurol Sci. 1994 May;123(1-2):74-9. doi: 10.1016/0022-510x(94)90206-2. J Neurol Sci. 1994. PMID: 8064325

4

Muscle mitochondria investigation in myotonic dystrophy.

Vita G, Toscano A, Prelle A, Bordoni A, Checcarelli N, Bresolin N, Baradello A, Messina C. Vita G, et al. Among authors: checcarelli n. Eur Neurol. 1993;33(6):423-7. doi: 10.1159/000116987. Eur Neurol. 1993. PMID: 8307063

5

Multiple deletions of mitochondrial DNA in a patient with periodic attacks of paralysis.

Prelle A, Moggio M, Checcarelli N, Comi G, Bresolin N, Battistel A, Bordoni A, Scarlato G. Prelle A, et al. Among authors: checcarelli n. J Neurol Sci. 1993 Jul;117(1-2):24-7. doi: 10.1016/0022-510x(93)90149-s. J Neurol Sci. 1993. PMID: 8410061

6

Congenital myopathy associated with abnormal accumulation of desmin and dystrophin.

Prelle A, Moggio M, Comi GP, Gallanti A, Checcarelli N, Bresolin N, Ciscato P, Fortunato F, Scarlato G. Prelle A, et al. Among authors: checcarelli n. Neuromuscul Disord. 1992;2(3):169-75. doi: 10.1016/0960-8966(92)90003-o. Neuromuscul Disord. 1992. PMID: 1483042

7

Desmin and vimentin as markers of regeneration in muscle diseases.

Gallanti A, Prelle A, Moggio M, Ciscato P, Checcarelli N, Sciacco M, Comini A, Scarlato G. Gallanti A, et al. Among authors: checcarelli n. Acta Neuropathol. 1992;85(1):88-92. doi: 10.1007/BF00304637. Acta Neuropathol. 1992. PMID: 1285499

8

Appearance and localization of dystrophin in normal human fetal muscle.

Prelle A, Chianese L, Moggio M, Gallanti A, Sciacco M, Checcarelli N, Comi G, Scarpini E, Bonilla E, Scarlato G. Prelle A, et al. Among authors: checcarelli n. Int J Dev Neurosci. 1991;9(6):607-12. doi: 10.1016/0736-5748(91)90022-e. Int J Dev Neurosci. 1991. PMID: 1803857

9

Anionic phospholipids calcium binding sites in Duchenne and murine X-linked muscular dystrophy.

Moggio M, Prelle A, Fagiolari G, Checcarelli N, Sciacco M, Ciscato P, Scarlato G. Moggio M, et al. Among authors: checcarelli n. Muscle Nerve. 1994 May;17(5):485-8. doi: 10.1002/mus.880170503. Muscle Nerve. 1994. PMID: 8159177

10

Critically ill patients: immunological evidence of inflammation in muscle biopsy.

Bazzi P, Moggio M, Prelle A, Sciacco M, Messina S, Barbieri S, Tonin P, Tomelleri G, Battistel A, Adobbati L, Checcarelli N, Veschi G, Scarlato G. Bazzi P, et al. Among authors: checcarelli n. Clin Neuropathol. 1999 Jan-Feb;18(1):23-30. Clin Neuropathol. 1999. PMID: 9988135

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