Fortunato F - Search Results

1

Mitochondrial respiratory chain dysfunction in muscle from patients with amyotrophic lateral sclerosis.

Crugnola V, Lamperti C, Lucchini V, Ronchi D, Peverelli L, Prelle A, Sciacco M, Bordoni A, Fassone E, Fortunato F, Corti S, Silani V, Bresolin N, Di Mauro S, Comi GP, Moggio M. Crugnola V, et al. Among authors: fortunato f. Arch Neurol. 2010 Jul;67(7):849-54. doi: 10.1001/archneurol.2010.128. Arch Neurol. 2010. PMID: 20625092

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

Muscle phosphoglycerate mutase (PGAM) deficiency in the first Caucasian patient: biochemistry, muscle culture and 31P-MR spectroscopy.

Vita G, Toscano A, Bresolin N, Meola G, Fortunato F, Baradello A, Barbiroli B, Frassineti C, Zaniol P, Messina C. Vita G, et al. Among authors: fortunato f. J Neurol. 1994 Mar;241(5):289-94. doi: 10.1007/BF00868435. J Neurol. 1994. PMID: 8006681

9

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

10

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

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