Bresolin N - Search Results

1

Progressive cytochrome c oxidase deficiency in a case of Kearns-Sayre syndrome: morphological, immunological, and biochemical studies in muscle biopsies and autopsy tissues.

Bresolin N, Moggio M, Bet L, Gallanti A, Prelle A, Nobile-Orazio E, Adobbati L, Ferrante C, Pellegrini G, Scarlato G. Bresolin N, et al. Ann Neurol. 1987 Jun;21(6):564-72. doi: 10.1002/ana.410210607. Ann Neurol. 1987. PMID: 3037990

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

3

Lipid storage myopathy in multiple acyl-CoA dehydrogenase deficiency: an adult case.

Mongini T, Doriguzzi C, Palmucci L, De Francesco A, Bet L, Manfredi L, Ponzetto C, Bresolin N. Mongini T, et al. Among authors: bresolin n. Eur Neurol. 1992;32(3):170-6. doi: 10.1159/000116817. Eur Neurol. 1992. PMID: 1592075

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. J Neurol Sci. 1991 Aug;104(2):182-9. doi: 10.1016/0022-510x(91)90308-t. J Neurol Sci. 1991. PMID: 1658240

5

In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria.

Chomyn A, Meola G, Bresolin N, Lai ST, Scarlato G, Attardi G. Chomyn A, et al. Among authors: bresolin n. Mol Cell Biol. 1991 Apr;11(4):2236-44. doi: 10.1128/mcb.11.4.2236-2244.1991. Mol Cell Biol. 1991. PMID: 1848674 Free PMC article.

6

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: bresolin n. Neurology. 1991 Aug;41(8):1211-5. doi: 10.1212/wnl.41.8.1211. Neurology. 1991. PMID: 1866007

7

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

8

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. Among authors: bresolin n. Rev Neurol (Paris). 1991;147(6-7):542-8. Rev Neurol (Paris). 1991. PMID: 1962062 Clinical Trial.

9

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

10

Ubidecarenone in the treatment of mitochondrial myopathies: a multi-center double-blind trial.

Bresolin N, Doriguzzi C, Ponzetto C, Angelini C, Moroni I, Castelli E, Cossutta E, Binda A, Gallanti A, Gabellini S, et al. Bresolin N, et al. J Neurol Sci. 1990 Dec;100(1-2):70-8. doi: 10.1016/0022-510x(90)90015-f. J Neurol Sci. 1990. PMID: 2089142 Clinical Trial.

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