Prelle A - Search Results

1

Lack of apoptosis in patients with progressive external ophthalmoplegia and mutated adenine nucleotide translocator-1 gene.

Fagiolari G, Sciacco M, Chiveri L, Lamperti C, Comi GP, Scarlato G, Moggio M, Prelle A. Fagiolari G, et al. Among authors: prelle a. Muscle Nerve. 2002 Aug;26(2):265-9. doi: 10.1002/mus.10172. Muscle Nerve. 2002. PMID: 12210391

2

Desmin and vimentin as markers of regeneration in muscle diseases.

Gallanti A, Prelle A, Moggio M, Ciscato P, Checcarelli N, Sciacco M, Comini A, Scarlato G. Gallanti A, et al. Among authors: prelle a. Acta Neuropathol. 1992;85(1):88-92. doi: 10.1007/BF00304637. Acta Neuropathol. 1992. PMID: 1285499

3

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

4

Dystrophin deficiency in a case of congenital myopathy.

Prelle A, Medori R, Moggio M, Chan HW, Gallanti A, Scarlato G, Bonilla E. Prelle A, et al. J Neurol. 1992 Feb;239(2):76-8. doi: 10.1007/BF00862976. J Neurol. 1992. PMID: 1552307

5

Lack of anionic phospholipid calcium binding sites in Duchenne muscular dystrophy.

Moggio M, Fagiolari G, Prelle A, Gallanti A, Sciacco M, Scarlato G. Moggio M, et al. Among authors: prelle a. Muscle Nerve. 1992 Mar;15(3):325-31. doi: 10.1002/mus.880150311. Muscle Nerve. 1992. PMID: 1557080

6

Congenital myopathy with type 2A muscle fiber uniformity and smallness.

Gallanti A, Prelle A, Chianese L, Barbieri S, Jann S, Schiaffino S, Comini A, Scarpini E, Pellegrini G, Moggio M, et al. Gallanti A, et al. Among authors: prelle a. Neuropediatrics. 1992 Feb;23(1):10-3. doi: 10.1055/s-2008-1071303. Neuropediatrics. 1992. PMID: 1565211

7

Appearance and localization of dystrophin in normal human fetal muscle.

Prelle A, Chianese L, Moggio M, Gallanti A, Sciacco M, Checcarelli N, Comi G, Scarpini E, Bonilla E, Scarlato G. Prelle A, et al. Int J Dev Neurosci. 1991;9(6):607-12. doi: 10.1016/0736-5748(91)90022-e. Int J Dev Neurosci. 1991. PMID: 1803857

8

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

9

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

10

Characterization of SV40-transformed human cells by immunofluorescence and fluorescent in situ hybridization techniques.

Prelle A, Moggio M, Fagiolari G, Scarlato G, Miranda A, Bonilla E. Prelle A, et al. Basic Appl Histochem. 1989;33(3):179-83. Basic Appl Histochem. 1989. PMID: 2554869

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