Bresolin N - Search Results

1

Clinical and genetic features of a cohort of patients with MFN2-related neuropathy.

Abati E, Manini A, Velardo D, Del Bo R, Napoli L, Rizzo F, Moggio M, Bresolin N, Bellone E, Bassi MT, D'Angelo MG, Comi GP, Corti S. Abati E, et al. Among authors: bresolin n. Sci Rep. 2022 Apr 13;12(1):6181. doi: 10.1038/s41598-022-10220-0. Sci Rep. 2022. PMID: 35418194 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 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

4

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.

5

Immunological and biochemical studies and pilot therapeutic trial with ubidecarenone in Kearns-Sayre patients.

Bresolin N, Bet L, Ferrante C, Binda A, Carenzi A, Moggio M, Comi G, Scarlato G. Bresolin N, et al. Adv Neurol. 1988;48:239-56. Adv Neurol. 1988. PMID: 3334786 No abstract available.

6

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

7

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: bresolin n. Clin Neuropathol. 1994 Sep-Oct;13(5):286-91. Clin Neuropathol. 1994. PMID: 7805313

8

Multiple deletions of mitochondrial DNA in sporadic and atypical cases of encephalomyopathy.

Checcarelli N, Prelle A, Moggio M, Comi G, Bresolin N, Papadimitriou A, Fagiolari G, Bordoni A, Scarlato G. Checcarelli N, et al. Among authors: bresolin n. J Neurol Sci. 1994 May;123(1-2):74-9. doi: 10.1016/0022-510x(94)90206-2. J Neurol Sci. 1994. PMID: 8064325

9

Clinical variability in Becker muscular dystrophy. Genetic, biochemical and immunohistochemical correlates.

Comi GP, Prelle A, Bresolin N, Moggio M, Bardoni A, Gallanti A, Vita G, Toscano A, Ferro MT, Bordoni A, et al. Comi GP, et al. Among authors: bresolin n. Brain. 1994 Feb;117 ( Pt 1):1-14. doi: 10.1093/brain/117.1.1-a. Brain. 1994. PMID: 8149204

10

Multiple deletions of mitochondrial DNA in a patient with periodic attacks of paralysis.

Prelle A, Moggio M, Checcarelli N, Comi G, Bresolin N, Battistel A, Bordoni A, Scarlato G. Prelle A, et al. Among authors: bresolin n. J Neurol Sci. 1993 Jul;117(1-2):24-7. doi: 10.1016/0022-510x(93)90149-s. J Neurol Sci. 1993. PMID: 8410061

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