Bresolin N - Search Results

1

Optic atrophy plus phenotype due to mutations in the OPA1 gene: two more Italian families.

Ranieri M, Del Bo R, Bordoni A, Ronchi D, Colombo I, Riboldi G, Cosi A, Servida M, Magri F, Moggio M, Bresolin N, Comi GP, Corti S. Ranieri M, et al. Among authors: bresolin n. J Neurol Sci. 2012 Apr 15;315(1-2):146-9. doi: 10.1016/j.jns.2011.12.002. Epub 2011 Dec 22. J Neurol Sci. 2012. PMID: 22197506 Free PMC article.

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

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

6

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

7

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.

8

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.

9

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.

10

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: bresolin n. J Neurol Sci. 1990 May;96(2-3):207-10. doi: 10.1016/0022-510x(90)90133-8. J Neurol Sci. 1990. PMID: 2376752

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