Fortunato F - Search Results

1

A G+1-->A transversion at the 5' splice site of intron 69 of the dystrophin gene causing the absence of peripheral nerve Dp116 and severe clinical involvement in a DMD patient.

Comi GP, Ciafaloni E, de Silva HA, Prelle A, Bardoni A, Rigoletto C, Robotti M, Bresolin N, Moggio M, Fortunato F. Comi GP, et al. Among authors: fortunato f. Hum Mol Genet. 1995 Nov;4(11):2171-4. doi: 10.1093/hmg/4.11.2171. Hum Mol Genet. 1995. PMID: 8589698 No abstract available.

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

Bezafibrate-induced myopathy: no evidence for defects in muscle metabolism.

Vita G, Toscano A, Mileto G, Pitrone F, Ferrò MT, Gagliardi E, Bresolin N, Fortunato F, Messina C. Vita G, et al. Among authors: fortunato f. Eur Neurol. 1993;33(2):168-72. doi: 10.1159/000116927. Eur Neurol. 1993. PMID: 8467827

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