Moggio M - Search Results

1

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

2

Progressive extrinsic ophthalmoplegia with peripheral neuropathy and storage of muscle glycogen.

Moggio M, Valli G, Cerri C, Scarlato G, Pellegrini G. Moggio M, et al. J Neurol. 1979 Jul 11;221(1):25-37. doi: 10.1007/BF00313167. J Neurol. 1979. PMID: 92534

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

4

Phenotypic and proliferative properties of Schwann cells from nerves of diabetic patients.

Scarpini E, Doronzo R, Baron P, Moggio M, Basellini A, Scarlato G. Scarpini E, et al. Among authors: moggio m. Int J Clin Pharmacol Res. 1992;12(5-6):211-5. Int J Clin Pharmacol Res. 1992. PMID: 1301402

5

Sural nerve immunoreactivity for nerve growth factor receptor in a case of localized hypertrophic neuropathy.

Sciacco M, Scarpini E, Baron PL, Doronzo R, Moggio M, Passerini D, Scarlato G. Sciacco M, et al. Among authors: moggio m. Acta Neuropathol. 1992;83(5):547-53. doi: 10.1007/BF00310035. Acta Neuropathol. 1992. PMID: 1320324

6

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

7

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: moggio m. J Neurol. 1992 Feb;239(2):76-8. doi: 10.1007/BF00862976. J Neurol. 1992. PMID: 1552307

8

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

9

Dystrophin deficiency in young girls with sporadic myopathy and normal karyotype.

Minetti C, Chang HW, Medori R, Prelle A, Moggio M, Johnsen SD, Bonilla E. Minetti C, et al. Among authors: moggio m. Neurology. 1991 Aug;41(8):1288-92. doi: 10.1212/wnl.41.8.1288. Neurology. 1991. PMID: 1714059

10

Lysosomotropic agents induce morphological and functional changes in human muscle cells in vitro.

Baron PL, Meola G, Scarpini E, Moggio M, Santilli I, Scarlato G. Baron PL, et al. Among authors: moggio m. Eur J Basic Appl Histochem. 1991;35(4):423-32. Eur J Basic Appl Histochem. 1991. PMID: 1801935

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