Moggio M - Search Results

1

Neural regulation of acid maltase in an unusual adult onset deficiency.

Meola G, Sansone V, Rotondo G, Radice S, Sterlicchio M, Mauri M, Bresolin N, Moggio M. Meola G, et al. Among authors: moggio m. Clin Neuropathol. 1994 Sep-Oct;13(5):286-91. Clin Neuropathol. 1994. PMID: 7805313

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

Lysosomotropic agents induce morphological and functional changes in human muscle cells in vitro.

Baron PL, Meola G, Scarpini E, Moggio M, Santilli I, Scarlato G. Baron PL, et al. Among authors: moggio m. Eur J Basic Appl Histochem. 1991;35(4):423-32. Eur J Basic Appl Histochem. 1991. PMID: 1801935

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

Cytochrome c oxidase during human fetal development.

Moggio M, Bresolin N, Scarpini E, Adobbati L, Prelle A, Gallanti A, Bet L, Fortunato F, Pellegrini G, Scarlato G. Moggio M, et al. Int J Dev Neurosci. 1989;7(1):5-14. doi: 10.1016/0736-5748(89)90040-3. Int J Dev Neurosci. 1989. PMID: 2540623

10

[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.

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