Gallanti A - Search Results

1

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. Neuropediatrics. 1992 Feb;23(1):10-3. doi: 10.1055/s-2008-1071303. Neuropediatrics. 1992. PMID: 1565211

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

3

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. Acta Neuropathol. 1992;85(1):88-92. doi: 10.1007/BF00304637. Acta Neuropathol. 1992. PMID: 1285499

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. Among authors: gallanti a. J Neurol. 1992 Feb;239(2):76-8. doi: 10.1007/BF00862976. J Neurol. 1992. PMID: 1552307

5

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. Among authors: gallanti a. Int J Dev Neurosci. 1991;9(6):607-12. doi: 10.1016/0736-5748(91)90022-e. Int J Dev Neurosci. 1991. PMID: 1803857

6

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

7

Ultrastructural localization of calcium binding sites on human muscle cell surface.

Moggio M, Jann S, Adobbati L, Prelle A, Gallanti A, Fagiolari G, Pellegrini G, Scarlato G. Moggio M, et al. Among authors: gallanti a. Muscle Nerve. 1989 Nov;12(11):910-4. doi: 10.1002/mus.880121107. Muscle Nerve. 1989. PMID: 2558316

8

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: gallanti a. Muscle Nerve. 1992 Mar;15(3):325-31. doi: 10.1002/mus.880150311. Muscle Nerve. 1992. PMID: 1557080

9

Clinical variability in Becker muscular dystrophy. Genetic, biochemical and immunohistochemical correlates.

Comi GP, Prelle A, Bresolin N, Moggio M, Bardoni A, Gallanti A, Vita G, Toscano A, Ferro MT, Bordoni A, et al. Comi GP, et al. Among authors: gallanti a. Brain. 1994 Feb;117 ( Pt 1):1-14. doi: 10.1093/brain/117.1.1-a. Brain. 1994. PMID: 8149204

10

Clinical, morphological and immunological evaluation of six patients with dysferlin deficiency.

Prelle A, Sciacco M, Tancredi L, Fagiolari G, Comi GP, Ciscato P, Serafini M, Fortunato F, Zecca C, Gallanti A, Chiveri L, Bresolin N, Scarlato G, Moggio M. Prelle A, et al. Among authors: gallanti a. Acta Neuropathol. 2003 Jun;105(6):537-42. doi: 10.1007/s00401-002-0654-1. Epub 2003 Mar 4. Acta Neuropathol. 2003. PMID: 12734659

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