Fortunato F - Search Results

1

Sarcoglycan deficiency in a large Italian population of myopathic patients.

Prelle A, Comi GP, Tancredi L, Rigoletto C, Ciscato P, Fortunato F, Nesti S, Sciacco M, Robotti M, Bazzi P, Felisari G, Moggio M, Scarlato G. Prelle A, et al. Among authors: fortunato f. Acta Neuropathol. 1998 Nov;96(5):509-14. doi: 10.1007/s004010050926. Acta Neuropathol. 1998. PMID: 9829815

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: fortunato f. Neuromuscul Disord. 1992;2(3):169-75. doi: 10.1016/0960-8966(92)90003-o. Neuromuscul Disord. 1992. PMID: 1483042

3

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: fortunato f. Enzyme. 1991;45(4):180-7. doi: 10.1159/000468887. Enzyme. 1991. PMID: 1823863

4

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

5

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: fortunato f. Int J Dev Neurosci. 1989;7(1):5-14. doi: 10.1016/0736-5748(89)90040-3. Int J Dev Neurosci. 1989. PMID: 2540623

6

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: fortunato f. J Neurol. 1989 May;236(4):193-8. doi: 10.1007/BF00314498. J Neurol. 1989. PMID: 2760630

7

Recessive carnitine palmityl transferase deficiency: biochemical studies in tissue cultures and platelets.

Meola G, Bresolin N, Rimoldi M, Velicogna M, Fortunato F, Scarlato G. Meola G, et al. Among authors: fortunato f. J Neurol. 1987 Dec;235(2):74-9. doi: 10.1007/BF00718013. J Neurol. 1987. PMID: 3430194

8

Chronic progressive external ophthalmoplegia: a correlative study of quantitative molecular data and histochemical and biochemical profile.

Fassati A, Bordoni A, Amboni P, Fortunato F, Fagiolari G, Bresolin N, Prelle A, Comi G, Scarlato G. Fassati A, et al. Among authors: fortunato f. J Neurol Sci. 1994 May;123(1-2):140-6. doi: 10.1016/0022-510x(94)90216-x. J Neurol Sci. 1994. PMID: 8064307

9

Clinical and biochemical evidence of skeletal muscle involvement in galactose-1-phosphate uridyl transferase deficiency.

Bresolin N, Comi GP, Fortunato F, Meola G, Gallanti A, Tajana A, Velicogna M, Gonano EF, Ninfali P, Pifferi S, et al. Bresolin N, et al. Among authors: fortunato f. J Neurol. 1993 May;240(5):272-7. doi: 10.1007/BF00838160. J Neurol. 1993. PMID: 8326330

10

Utrophin expression during human fetal development.

Rigoletto C, Prelle A, Ciscato P, Moggio M, Comi G, Fortunato F, Scarlato G. Rigoletto C, et al. Among authors: fortunato f. Int J Dev Neurosci. 1995 Oct;13(6):585-93. doi: 10.1016/0736-5748(95)00039-j. Int J Dev Neurosci. 1995. PMID: 8553893

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