Scarlato G - Search Results

1

Nucleus-driven multiple large-scale deletions of the human mitochondrial genome: a new autosomal dominant disease.

Zeviani M, Bresolin N, Gellera C, Bordoni A, Pannacci M, Amati P, Moggio M, Servidei S, Scarlato G, DiDonato S. Zeviani M, et al. Among authors: scarlato g. Am J Hum Genet. 1990 Dec;47(6):904-14. Am J Hum Genet. 1990. PMID: 1978558 Free PMC article.

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

[Mitochondrial encephalomyopathy].

Scarlato G, Bresolin N, Moggio M, Bet L, Meola G. Scarlato G, et al. Recenti Prog Med. 1989 Dec;80(12):665-72. Recenti Prog Med. 1989. PMID: 2560839 Italian.

4

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

5

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

6

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

7

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

8

Retrospective study of a large population of patients affected with mitochondrial disorders: clinical, morphological and molecular genetic evaluation.

Sciacco M, Prelle A, Comi GP, Napoli L, Battistel A, Bresolin N, Tancredi L, Lamperti C, Bordoni A, Fagiolari G, Ciscato P, Chiveri L, Perini MP, Fortunato F, Adobbati L, Messina S, Toscano A, Martinelli-Boneschi F, Papadimitriou A, Scarlato G, Moggio M. Sciacco M, et al. Among authors: scarlato g. J Neurol. 2001 Sep;248(9):778-88. doi: 10.1007/s004150170094. J Neurol. 2001. PMID: 11596783

9

Muscle biopsy in Alzheimer's disease: morphological and biochemical findings.

Mariani C, Bresolin N, Farina E, Moggio M, Ferrante C, Ciafaloni E, Sertorelli S, Ciccone A, Scarlato G. Mariani C, et al. Among authors: scarlato g. Clin Neuropathol. 1991 Jul-Aug;10(4):171-6. Clin Neuropathol. 1991. PMID: 1884524

10

Multicenter trial with ubidecarenone: treatment of 44 patients with mitochondrial myopathies.

Scarlato G, Bresolin N, Moroni I, Doriguzzi C, Castelli E, Comi G, Angelini C, Carenzi A. Scarlato G, et al. Rev Neurol (Paris). 1991;147(6-7):542-8. Rev Neurol (Paris). 1991. PMID: 1962062 Clinical Trial.

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