Bardoni A - Search Results

1

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

2

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: bardoni a. Neuromuscul Disord. 1994 Jul;4(4):359-69. doi: 10.1016/0960-8966(94)90072-8. Neuromuscul Disord. 1994. PMID: 7981593

3

Duplication of dystrophin gene and dissimilar clinical phenotype in the same family.

Toscano A, Vitiello L, Comi GP, Galvagni F, Miorin M, Prelle A, Fortunato F, Bardoni A, Mora M, Fiumara A, et al. Toscano A, et al. Among authors: bardoni a. Neuromuscul Disord. 1995 Nov;5(6):475-81. doi: 10.1016/0960-8966(95)00008-b. Neuromuscul Disord. 1995. PMID: 8580729

4

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: bardoni a. 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.

5

Absence of brain Dp140 isoform and cognitive impairment in Becker muscular dystrophy.

Bardoni A, Sironi M, Felisari G, Comi GP, Bresolin N. Bardoni A, et al. Lancet. 1999 Mar 13;353(9156):897-8. doi: 10.1016/S0140-6736(98)05801-2. Lancet. 1999. PMID: 10093987 No abstract available.

6

Loss of Dp140 dystrophin isoform and intellectual impairment in Duchenne dystrophy.

Felisari G, Martinelli Boneschi F, Bardoni A, Sironi M, Comi GP, Robotti M, Turconi AC, Lai M, Corrao G, Bresolin N. Felisari G, et al. Among authors: bardoni a. Neurology. 2000 Aug 22;55(4):559-64. doi: 10.1212/wnl.55.4.559. Neurology. 2000. PMID: 10953192

7

Primary beta-sarcoglycanopathy manifesting as recurrent exercise-induced myoglobinuria.

Cagliani R, Comi GP, Tancredi L, Sironi M, Fortunato F, Giorda R, Bardoni A, Moggio M, Prelle A, Bresolin N, Scarlato G. Cagliani R, et al. Among authors: bardoni a. Neuromuscul Disord. 2001 May;11(4):389-94. doi: 10.1016/s0960-8966(00)00207-8. Neuromuscul Disord. 2001. PMID: 11369190

8

Transcriptional activation of the non-muscle, full-length dystrophin isoforms in Duchenne muscular dystrophy skeletal muscle.

Sironi M, Bardoni A, Felisari G, Cagliani R, Robotti M, Comi GP, Moggio M, Bresolin N. Sironi M, et al. Among authors: bardoni a. J Neurol Sci. 2001 May 1;186(1-2):51-7. doi: 10.1016/s0022-510x(01)00502-0. J Neurol Sci. 2001. PMID: 11412872

9

An intragenic deletion/inversion event in the DMD gene determines a novel exon creation and results in a BMD phenotype.

Cagliani R, Sironi M, Ciafaloni E, Bardoni A, Fortunato F, Prelle A, Serafini M, Bresolin N, Comi GP. Cagliani R, et al. Among authors: bardoni a. Hum Genet. 2004 Jun;115(1):13-8. doi: 10.1007/s00439-004-1118-6. Epub 2004 Apr 30. Hum Genet. 2004. PMID: 15118904

10

Loss of Dp140 regulatory sequences is associated with cognitive impairment in dystrophinopathies.

Bardoni A, Felisari G, Sironi M, Comi G, Lai M, Robotti M, Bresolin N. Bardoni A, et al. Neuromuscul Disord. 2000 Mar;10(3):194-9. doi: 10.1016/s0960-8966(99)00108-x. Neuromuscul Disord. 2000. PMID: 10734267

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