Scarlato G - Search Results

1

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. Among authors: scarlato g. J Neurol Sci. 1994 May;123(1-2):74-9. doi: 10.1016/0022-510x(94)90206-2. J Neurol Sci. 1994. PMID: 8064325

2

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. Among authors: scarlato g. 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

3

Muscle mitochondrial DNA deletion and 31P-NMR spectroscopy alterations in a migraine patient.

Bresolin N, Martinelli P, Barbiroli B, Zaniol P, Ausenda C, Montagna P, Gallanti A, Comi GP, Scarlato G, Lugaresi E. Bresolin N, et al. Among authors: scarlato g. J Neurol Sci. 1991 Aug;104(2):182-9. doi: 10.1016/0022-510x(91)90308-t. J Neurol Sci. 1991. PMID: 1658240

4

Kearns-Sayre syndrome: different amounts of deleted mitochondrial DNA are present in several autoptic tissues.

Ponzetto C, Bresolin N, Bordoni A, Moggio M, Meola G, Bet L, Prelle A, Scarlato G. Ponzetto C, et al. Among authors: scarlato g. J Neurol Sci. 1990 May;96(2-3):207-10. doi: 10.1016/0022-510x(90)90133-8. J Neurol Sci. 1990. PMID: 2376752

5

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: scarlato g. J Neurol. 1994 Jul;241(8):511-6. doi: 10.1007/BF00919714. J Neurol. 1994. PMID: 7964921

6

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: scarlato g. Acta Neuropathol. 1994;87(4):371-6. doi: 10.1007/BF00313606. Acta Neuropathol. 1994. PMID: 8017172

7

Chronic progressive external ophthalmoplegia: a correlative study of quantitative molecular data and histochemical and biochemical profile.

Fassati A, Bordoni A, Amboni P, Fortunato F, Fagiolari G, Bresolin N, Prelle A, Comi G, Scarlato G. Fassati A, et al. Among authors: scarlato g. J Neurol Sci. 1994 May;123(1-2):140-6. doi: 10.1016/0022-510x(94)90216-x. J Neurol Sci. 1994. PMID: 8064307

8

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: scarlato g. J Neurol Sci. 1993 Jul;117(1-2):24-7. doi: 10.1016/0022-510x(93)90149-s. J Neurol Sci. 1993. PMID: 8410061

9

Asymptomatic familial hyperCKemia associated with desmin accumulation in skeletal muscle.

Prelle A, Rigoletto C, Moggio M, Sciacco M, Comi GP, Ciscato P, Fagiolari G, Rapuzzi S, Bignotti V, Scarlato G. Prelle A, et al. Among authors: scarlato g. J Neurol Sci. 1996 Sep 1;140(1-2):132-6. doi: 10.1016/0022-510x(96)00129-3. J Neurol Sci. 1996. PMID: 8866439

10

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: scarlato 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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