Pellegrini G - Search Results

1

Biochemical and immunologic studies in a case of congenital myopathy with unusual morphologic features.

Biral D, Damiani E, Scarpini E, Bet L, Bresolin N, Moggio M, Pellegrini G, Barbieri S, Scarlato G. Biral D, et al. Among authors: pellegrini g. Neurology. 1987 Oct;37(10):1658-62. doi: 10.1212/wnl.37.10.1658. Neurology. 1987. PMID: 3309721

2

A hereditary case of lipid storage myopathy with carnitine deficiency. Ultrastructural observation of muscle tissue in parents.

Pellegrini G, Scarlato G, Moggio M. Pellegrini G, et al. J Neurol. 1980;223(2):73-84. doi: 10.1007/BF00313171. J Neurol. 1980. PMID: 6157005

3

Fast to slow change of myosin in nemaline myopathy: electrophoretic and immunologic evidence.

Volpe P, Damiani E, Margreth A, Pellegrini G, Scarlato G. Volpe P, et al. Among authors: pellegrini g. Neurology. 1982 Jan;32(1):37-41. doi: 10.1212/wnl.32.1.37. Neurology. 1982. PMID: 7198731

4

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. Among authors: pellegrini g. J Neurol. 1979 Jul 11;221(1):25-37. doi: 10.1007/BF00313167. J Neurol. 1979. PMID: 92534

5

Morphologic and metabolic studies in a case of oculo-cranio-somatic neuromuscular disease.

Scarlato G, Pellegrini G, Veicsteinas A. Scarlato G, et al. Among authors: pellegrini g. J Neuropathol Exp Neurol. 1978 Jan;37(1):1-12. doi: 10.1097/00005072-197801000-00001. J Neuropathol Exp Neurol. 1978. PMID: 619006

6

Progressive cytochrome c oxidase deficiency in a case of Kearns-Sayre syndrome: morphological, immunological, and biochemical studies in muscle biopsies and autopsy tissues.

Bresolin N, Moggio M, Bet L, Gallanti A, Prelle A, Nobile-Orazio E, Adobbati L, Ferrante C, Pellegrini G, Scarlato G. Bresolin N, et al. Among authors: pellegrini g. Ann Neurol. 1987 Jun;21(6):564-72. doi: 10.1002/ana.410210607. Ann Neurol. 1987. PMID: 3037990

7

A case of congenital neuromuscular disease with uniform type I fibers, abnormal mitochondrial network and jagged Z-line.

Pellegrini G, Barbieri S, Moggio M, Cheldi A, Scarlato G, Minetti C. Pellegrini G, et al. Neuropediatrics. 1985 Aug;16(3):162-6. doi: 10.1055/s-2008-1059533. Neuropediatrics. 1985. PMID: 4047349

8

Bilateral exophthalmic ophthalmoplegia. A case report.

Scarlato G, Pellegrini G. Scarlato G, et al. Among authors: pellegrini g. Eur Neurol. 1969;2(5):285-95. doi: 10.1159/000113805. Eur Neurol. 1969. PMID: 5394300 No abstract available.

9

[Hypothyroid myopathy: histochemical and ultrastructural features with physiopatological correlations (author's transl)].

Pellegrini G, Moggio M. Pellegrini G, et al. Riv Patol Nerv Ment. 1979 Jun;99(5):275-88. Riv Patol Nerv Ment. 1979. PMID: 159485 Italian.

10

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

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