Bresolin N - Search Results

1

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. Neurology. 1988 Jun;38(6):892-9. doi: 10.1212/wnl.38.6.892. Neurology. 1988. PMID: 3368070

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

[Expression of a defect in the respiratory chain in cultured human cells].

Meola G, Rotondo G, Velicogna M, Toppi R, Sansone V, Bresolin N, Comi G, Bordoni A, Amati P, Ausenda C, et al. Meola G, et al. Among authors: bresolin n. Riv Neurol. 1991 Jul-Aug;61(4):122-34. Riv Neurol. 1991. PMID: 1667713 Italian.

6

Glucose-6-phosphate dehydrogenase Lodi844C: a study on its expression in blood cells and muscle.

Ninfali P, Bresolin N, Baronciani L, Fortunato F, Comi G, Magnani M, Scarlato G. Ninfali P, et al. Among authors: bresolin n. Enzyme. 1991;45(4):180-7. doi: 10.1159/000468887. Enzyme. 1991. PMID: 1823863

7

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.

8

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

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

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