Moggio M - Search Results

1

POLG1 mutations and stroke like episodes: a distinct clinical entity rather than an atypical MELAS syndrome.

Cheldi A, Ronchi D, Bordoni A, Bordo B, Lanfranconi S, Bellotti MG, Corti S, Lucchini V, Sciacco M, Moggio M, Baron P, Comi GP, Colombo A, Bersano A; Lombardia GENS collaborators. Cheldi A, et al. Among authors: moggio m. BMC Neurol. 2013 Jan 15;13:8. doi: 10.1186/1471-2377-13-8. BMC Neurol. 2013. PMID: 23324391 Free PMC article.

2

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: moggio m. Int J Dev Neurosci. 1991;9(6):607-12. doi: 10.1016/0736-5748(91)90022-e. Int J Dev Neurosci. 1991. PMID: 1803857

3

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: moggio m. Am J Hum Genet. 1990 Dec;47(6):904-14. Am J Hum Genet. 1990. PMID: 1978558 Free PMC article.

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: moggio m. 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

Muscle glucose-6-phosphate dehydrogenase deficiency.

Bresolin N, Bet L, Moggio M, Meola G, Fortunato F, Comi G, Adobbati L, Geremia L, Pittalis S, Scarlato G. Bresolin N, et al. Among authors: moggio m. J Neurol. 1989 May;236(4):193-8. doi: 10.1007/BF00314498. J Neurol. 1989. PMID: 2760630

6

Immunological and biochemical studies and pilot therapeutic trial with ubidecarenone in Kearns-Sayre patients.

Bresolin N, Bet L, Ferrante C, Binda A, Carenzi A, Moggio M, Comi G, Scarlato G. Bresolin N, et al. Among authors: moggio m. Adv Neurol. 1988;48:239-56. Adv Neurol. 1988. PMID: 3334786 No abstract available.

7

Clinical and biochemical correlations in mitochondrial myopathies treated with coenzyme Q10.

Bresolin N, Bet L, Binda A, Moggio M, Comi G, Nador F, Ferrante C, Carenzi A, Scarlato G. Bresolin N, et al. Among authors: moggio m. Neurology. 1988 Jun;38(6):892-9. doi: 10.1212/wnl.38.6.892. Neurology. 1988. PMID: 3368070

8

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

9

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

10

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

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