Bresolin N - Search Results

1

Cognitive impairment in Duchenne muscular dystrophy.

Bresolin N, Castelli E, Comi GP, Felisari G, Bardoni A, Perani D, Grassi F, Turconi A, Mazzucchelli F, Gallotti D, et al. Bresolin N, et al. Neuromuscul Disord. 1994 Jul;4(4):359-69. doi: 10.1016/0960-8966(94)90072-8. Neuromuscul Disord. 1994. PMID: 7981593

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

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.

6

Endocrine involvement in mitochondrial encephalomyopathy with partial cytochrome c oxidase deficiency.

Doriguzzi C, Palmucci L, Mongini T, Bresolin N, Bet L, Comi G, Lala R. Doriguzzi C, et al. Among authors: bresolin n. J Neurol Neurosurg Psychiatry. 1989 Jan;52(1):122-5. doi: 10.1136/jnnp.52.1.122. J Neurol Neurosurg Psychiatry. 1989. PMID: 2540284 Free PMC article.

7

Muscle glucose-6-phosphate dehydrogenase deficiency.

Bresolin N, Bet L, Moggio M, Meola G, Fortunato F, Comi G, Adobbati L, Geremia L, Pittalis S, Scarlato G. Bresolin N, et al. J Neurol. 1989 May;236(4):193-8. doi: 10.1007/BF00314498. J Neurol. 1989. PMID: 2760630

8

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

9

Ryanodine receptor gene point mutation and malignant hyperthermia susceptibility.

Moroni I, Gonano EF, Comi GP, Tegazzin V, Prelle A, Bordoni A, Bresolin N, Scarlato G. Moroni I, et al. Among authors: bresolin n. J Neurol. 1995 Feb;242(3):127-33. doi: 10.1007/BF00936884. J Neurol. 1995. PMID: 7751854

10

Multiple sclerosis and mitochondrial myopathy: an unusual combination of diseases.

Bet L, Moggio M, Comi GP, Mariani C, Prelle A, Checcarelli N, Bordoni A, Bresolin N, Scarpini E, Scarlato G. Bet L, et al. Among authors: bresolin n. J Neurol. 1994 Jul;241(8):511-6. doi: 10.1007/BF00919714. J Neurol. 1994. PMID: 7964921

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