Bet L - Search Results

1

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. J Neurol. 1994 Jul;241(8):511-6. doi: 10.1007/BF00919714. J Neurol. 1994. PMID: 7964921

2

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

3

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. Among authors: bet l. J Neurol. 1989 May;236(4):193-8. doi: 10.1007/BF00314498. J Neurol. 1989. PMID: 2760630

4

Biochemical and immunologic studies in a case of congenital myopathy with unusual morphologic features.

Biral D, Damiani E, Scarpini E, Bet L, Bresolin N, Moggio M, Pellegrini G, Barbieri S, Scarlato G. Biral D, et al. Among authors: bet l. Neurology. 1987 Oct;37(10):1658-62. doi: 10.1212/wnl.37.10.1658. Neurology. 1987. PMID: 3309721

5

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

6

Early-onset cerebellar ataxia, myoclonus and hypogonadism in a case of mitochondrial complex III deficiency treated with vitamins K3 and C.

Toscano A, Fazio MC, Vita G, Cannavó S, Bresolin N, Bet L, Prelle A, Barbiroli B, Iotti S, Zaniol P, et al. Toscano A, et al. Among authors: bet l. J Neurol. 1995 Mar;242(4):203-9. doi: 10.1007/BF00919592. J Neurol. 1995. PMID: 7798118

7

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: bet l. Eur Neurol. 1992;32(3):170-6. doi: 10.1159/000116817. Eur Neurol. 1992. PMID: 1592075

8

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

9

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: bet l. 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.

10

Cytochrome c oxidase during human fetal development.

Moggio M, Bresolin N, Scarpini E, Adobbati L, Prelle A, Gallanti A, Bet L, Fortunato F, Pellegrini G, Scarlato G. Moggio M, et al. Among authors: bet l. Int J Dev Neurosci. 1989;7(1):5-14. doi: 10.1016/0736-5748(89)90040-3. Int J Dev Neurosci. 1989. PMID: 2540623

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