Comi GP - Search Results

1

Autologous transplantation of muscle-derived CD133+ stem cells in Duchenne muscle patients.

Torrente Y, Belicchi M, Marchesi C, D'Antona G, Cogiamanian F, Pisati F, Gavina M, Giordano R, Tonlorenzi R, Fagiolari G, Lamperti C, Porretti L, Lopa R, Sampaolesi M, Vicentini L, Grimoldi N, Tiberio F, Songa V, Baratta P, Prelle A, Forzenigo L, Guglieri M, Pansarasa O, Rinaldi C, Mouly V, Butler-Browne GS, Comi GP, Biondetti P, Moggio M, Gaini SM, Stocchetti N, Priori A, D'Angelo MG, Turconi A, Bottinelli R, Cossu G, Rebulla P, Bresolin N. Torrente Y, et al. Among authors: comi gp. Cell Transplant. 2007;16(6):563-77. doi: 10.3727/000000007783465064. Cell Transplant. 2007. PMID: 17912948 Free article. Clinical Trial.

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

3

Muscle mitochondrial DNA deletion and 31P-NMR spectroscopy alterations in a migraine patient.

Bresolin N, Martinelli P, Barbiroli B, Zaniol P, Ausenda C, Montagna P, Gallanti A, Comi GP, Scarlato G, Lugaresi E. Bresolin N, et al. Among authors: comi gp. J Neurol Sci. 1991 Aug;104(2):182-9. doi: 10.1016/0022-510x(91)90308-t. J Neurol Sci. 1991. PMID: 1658240

4

Multiple sclerosis and mitochondrial myopathy: an unusual combination of diseases.

Bet L, Moggio M, Comi GP, Mariani C, Prelle A, Checcarelli N, Bordoni A, Bresolin N, Scarpini E, Scarlato G. Bet L, et al. Among authors: comi gp. J Neurol. 1994 Jul;241(8):511-6. doi: 10.1007/BF00919714. J Neurol. 1994. PMID: 7964921

5

Cognitive impairment in Duchenne muscular dystrophy.

Bresolin N, Castelli E, Comi GP, Felisari G, Bardoni A, Perani D, Grassi F, Turconi A, Mazzucchelli F, Gallotti D, et al. Bresolin N, et al. Among authors: comi gp. Neuromuscul Disord. 1994 Jul;4(4):359-69. doi: 10.1016/0960-8966(94)90072-8. Neuromuscul Disord. 1994. PMID: 7981593

6

Mitochondrial myopathy: correlation between oxidative defect and mitochondrial DNA deletions at single fiber level.

Prelle A, Fagiolari G, Checcarelli N, Moggio M, Battistel A, Comi GP, Bazzi P, Bordoni A, Zeviani M, Scarlato G. Prelle A, et al. Among authors: comi gp. Acta Neuropathol. 1994;87(4):371-6. doi: 10.1007/BF00313606. Acta Neuropathol. 1994. PMID: 8017172

7

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. Brain. 1994 Feb;117 ( Pt 1):1-14. doi: 10.1093/brain/117.1.1-a. Brain. 1994. PMID: 8149204

8

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: comi gp. J Neurol. 1993 May;240(5):272-7. doi: 10.1007/BF00838160. J Neurol. 1993. PMID: 8326330

9

A G+1-->A transversion at the 5' splice site of intron 69 of the dystrophin gene causing the absence of peripheral nerve Dp116 and severe clinical involvement in a DMD patient.

Comi GP, Ciafaloni E, de Silva HA, Prelle A, Bardoni A, Rigoletto C, Robotti M, Bresolin N, Moggio M, Fortunato F. Comi GP, et al. Hum Mol Genet. 1995 Nov;4(11):2171-4. doi: 10.1093/hmg/4.11.2171. Hum Mol Genet. 1995. PMID: 8589698 No abstract available.

10

Asymptomatic familial hyperCKemia associated with desmin accumulation in skeletal muscle.

Prelle A, Rigoletto C, Moggio M, Sciacco M, Comi GP, Ciscato P, Fagiolari G, Rapuzzi S, Bignotti V, Scarlato G. Prelle A, et al. Among authors: comi gp. J Neurol Sci. 1996 Sep 1;140(1-2):132-6. doi: 10.1016/0022-510x(96)00129-3. J Neurol Sci. 1996. PMID: 8866439

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