Bresolin N - Search Results

1

Gene therapy rescues disease phenotype in a spinal muscular atrophy with respiratory distress type 1 (SMARD1) mouse model.

Nizzardo M, Simone C, Rizzo F, Salani S, Dametti S, Rinchetti P, Del Bo R, Foust K, Kaspar BK, Bresolin N, Comi GP, Corti S. Nizzardo M, et al. Among authors: bresolin n. Sci Adv. 2015 Mar 13;1(2):e1500078. doi: 10.1126/sciadv.1500078. eCollection 2015 Mar. Sci Adv. 2015. PMID: 26601156 Free PMC article.

2

Multicenter trial with ubidecarenone: treatment of 44 patients with mitochondrial myopathies.

Scarlato G, Bresolin N, Moroni I, Doriguzzi C, Castelli E, Comi G, Angelini C, Carenzi A. Scarlato G, et al. Among authors: bresolin n. Rev Neurol (Paris). 1991;147(6-7):542-8. Rev Neurol (Paris). 1991. PMID: 1962062 Clinical Trial.

3

Immunological and biochemical studies and pilot therapeutic trial with ubidecarenone in Kearns-Sayre patients.

Bresolin N, Bet L, Ferrante C, Binda A, Carenzi A, Moggio M, Comi G, Scarlato G. Bresolin N, et al. Adv Neurol. 1988;48:239-56. Adv Neurol. 1988. PMID: 3334786 No abstract available.

4

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

5

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

6

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. Among authors: bresolin n. 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.

7

In vivo biolistic technique in control and mdx dystrophic mice.

Ausenda CD, Bresolin N, De Liso A, D'Angelo MG, Moggio M, Del Bo R, Gallanti A, Comi GP, Torrente Y, Bordoni A, Scarlato G. Ausenda CD, et al. Among authors: bresolin n. Muscle Nerve. 1996 Jul;19(7):912-4. doi: 10.1002/(SICI)1097-4598(199607)19:7<912::AID-MUS18>3.0.CO;2-K. Muscle Nerve. 1996. PMID: 8965850 No abstract available.

8

Intra-aortic injection of myoblasts in mdx mice: genetic and technetium-99m cell labeling and biodistribution.

Bresolin N, Ausenda CD, Casati R, Torrente Y, DeLiso A, D'Angelo MG, Benti R, Moggio M, Baldessari S, Comi GP, Colombo F, Gerundini P, Scarlato G. Bresolin N, et al. Muscle Nerve. 1997 Jun;20(6):757-9. doi: 10.1002/(sici)1097-4598(199706)20:6<757::aid-mus17>3.0.co;2-r. Muscle Nerve. 1997. PMID: 9149087 No abstract available.

9

Cytochrome c oxidase subunit I microdeletion in a patient with motor neuron disease.

Comi GP, Bordoni A, Salani S, Franceschina L, Sciacco M, Prelle A, Fortunato F, Zeviani M, Napoli L, Bresolin N, Moggio M, Ausenda CD, Taanman JW, Scarlato G. Comi GP, et al. Among authors: bresolin n. Ann Neurol. 1998 Jan;43(1):110-6. doi: 10.1002/ana.410430119. Ann Neurol. 1998. PMID: 9450776

10

Partial depletion and multiple deletions of muscle mtDNA in familial MNGIE syndrome.

Papadimitriou A, Comi GP, Hadjigeorgiou GM, Bordoni A, Sciacco M, Napoli L, Prelle A, Moggio M, Fagiolari G, Bresolin N, Salani S, Anastasopoulos I, Giassakis G, Divari R, Scarlato G. Papadimitriou A, et al. Among authors: bresolin n. Neurology. 1998 Oct;51(4):1086-92. doi: 10.1212/wnl.51.4.1086. Neurology. 1998. PMID: 9781534

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