Scarlato G - Search Results

1

The apolipoprotein E epsilon4 allele causes a faster decline of cognitive performances in Down's syndrome subjects.

Del Bo R, Comi GP, Bresolin N, Castelli E, Conti E, Degiuli A, Ausenda CD, Scarlato G. Del Bo R, et al. Among authors: scarlato g. J Neurol Sci. 1997 Jan;145(1):87-91. doi: 10.1016/s0022-510x(96)00249-3. J Neurol Sci. 1997. PMID: 9073034

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

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. Among authors: scarlato g. J Neurol. 2003 Jun;250(6):688-92. doi: 10.1007/s00415-003-1057-5. J Neurol. 2003. PMID: 12796830

4

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

5

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

6

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

7

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. Among authors: scarlato g. Ann Neurol. 2001 Jan;49(1):137-8. doi: 10.1002/1531-8249(200101)49:1<137::aid-ana26>3.0.co;2-i. Ann Neurol. 2001. PMID: 11198288 No abstract available.

8

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

9

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

10

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

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