Bresolin N - Search Results

1

A G+1-->A transversion at the 5' splice site of intron 69 of the dystrophin gene causing the absence of peripheral nerve Dp116 and severe clinical involvement in a DMD patient.

Comi GP, Ciafaloni E, de Silva HA, Prelle A, Bardoni A, Rigoletto C, Robotti M, Bresolin N, Moggio M, Fortunato F. Comi GP, et al. Among authors: bresolin n. Hum Mol Genet. 1995 Nov;4(11):2171-4. doi: 10.1093/hmg/4.11.2171. Hum Mol Genet. 1995. PMID: 8589698 No abstract available.

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

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

4

[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.

5

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

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

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: bresolin n. J Neurol. 1990 Nov;237(7):399-404. doi: 10.1007/BF00314729. J Neurol. 1990. PMID: 2125637

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