Moggio M - Search Results

1

Mitochondrial DNA G8363A mutation in the tRNA Lys gene: clinical, biochemical and pathological study.

Virgilio R, Ronchi D, Bordoni A, Fassone E, Bonato S, Donadoni C, Torgano G, Moggio M, Corti S, Bresolin N, Comi GP. Virgilio R, et al. Among authors: moggio m. J Neurol Sci. 2009 Jun 15;281(1-2):85-92. doi: 10.1016/j.jns.2009.01.025. Epub 2009 Mar 10. J Neurol Sci. 2009. PMID: 19278689 Review.

2

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: moggio m. Neuromuscul Disord. 1992;2(3):169-75. doi: 10.1016/0960-8966(92)90003-o. Neuromuscul Disord. 1992. PMID: 1483042

3

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

4

Leber's hereditary optic neuropathy: genetic, biochemical, and phosphorus magnetic resonance spectroscopy study in an Italian family.

Cortelli P, Montagna P, Avoni P, Sangiorgi S, Bresolin N, Moggio M, Zaniol P, Mantovani V, Barboni P, Barbiroli B, et al. Cortelli P, et al. Among authors: moggio m. Neurology. 1991 Aug;41(8):1211-5. doi: 10.1212/wnl.41.8.1211. Neurology. 1991. PMID: 1866007

5

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: moggio m. Clin Neuropathol. 1991 Jul-Aug;10(4):171-6. Clin Neuropathol. 1991. PMID: 1884524

6

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.

7

A case of mitochondrial myopathy, lactic acidosis and complex I deficiency.

Bet L, Bresolin N, Moggio M, Meola G, Prelle A, Schapira AH, Binzoni T, Chomyn A, Fortunato F, Cerretelli P, et al. Bet L, et al. Among authors: moggio m. J Neurol. 1990 Nov;237(7):399-404. doi: 10.1007/BF00314729. J Neurol. 1990. PMID: 2125637

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: 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

9

[Mitochondrial encephalomyopathy].

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

10

Normal muscle mitochondrial function in Ramsay-Hunt syndrome.

Sacquegna T, Montagna P, Moggio M, De Carolis P, Agati R, Bresolin N. Sacquegna T, et al. Among authors: moggio m. Ital J Neurol Sci. 1989 Feb;10(1):73-5. doi: 10.1007/BF02333875. Ital J Neurol Sci. 1989. PMID: 2925347

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