Mantegazza R - Search Results

1

Multidisciplinary study of a new ClC-1 mutation causing myotonia congenita: a paradigm to understand and treat ion channelopathies.

Imbrici P, Altamura C, Camerino GM, Mangiatordi GF, Conte E, Maggi L, Brugnoni R, Musaraj K, Caloiero R, Alberga D, Marsano RM, Ricci G, Siciliano G, Nicolotti O, Mora M, Bernasconi P, Desaphy JF, Mantegazza R, Camerino DC. Imbrici P, et al. Among authors: mantegazza r. FASEB J. 2016 Oct;30(10):3285-3295. doi: 10.1096/fj.201500079R. Epub 2016 Jun 20. FASEB J. 2016. PMID: 27324117 Free PMC article.

., Camerino, G. M., Mangiatordi, G. F., Conte, E., Maggi, L., Brugnoni, R., Musaraj, K., Caloiero, R., Alberga, D., Marsano, R. M., Ricci, G., Siciliano, G., Nicolotti, O., Mora, M., Bernasconi, P., Desaphy, J.-F., Mantegazza, R., Camerino, D. C …

., Camerino, G. M., Mangiatordi, G. F., Conte, E., Maggi, L., Brugnoni, R., Musaraj, K., Caloiero, R., Alberga, D., Marsano, …

2

Chloroquine myopathy and myasthenia-like syndrome.

Sghirlanzoni A, Mantegazza R, Mora M, Pareyson D, Cornelio F. Sghirlanzoni A, et al. Among authors: mantegazza r. Muscle Nerve. 1988 Feb;11(2):114-9. doi: 10.1002/mus.880110205. Muscle Nerve. 1988. PMID: 3343986

3

Lack of mRNA and dystrophin expression in DMD patients three months after myoblast transfer.

Morandi L, Bernasconi P, Gebbia M, Mora M, Crosti F, Mantegazza R, Cornelio F. Morandi L, et al. Among authors: mantegazza r. Neuromuscul Disord. 1995 Jul;5(4):291-5. doi: 10.1016/0960-8966(94)00070-p. Neuromuscul Disord. 1995. PMID: 7580241

4

Expression of transforming growth factor-beta 1 in dystrophic patient muscles correlates with fibrosis. Pathogenetic role of a fibrogenic cytokine.

Bernasconi P, Torchiana E, Confalonieri P, Brugnoni R, Barresi R, Mora M, Cornelio F, Morandi L, Mantegazza R. Bernasconi P, et al. Among authors: mantegazza r. J Clin Invest. 1995 Aug;96(2):1137-44. doi: 10.1172/JCI118101. J Clin Invest. 1995. PMID: 7635950 Free PMC article.

5

T-cell receptor-CDR3 sequences of polymyositis muscle-infiltrating T-lymphocytes indicate a conventional antigen as target.

Bernasconi P, Torchiana E, Baggi F, Andreetta F, Cornelio F, Mantegazza R. Bernasconi P, et al. Among authors: mantegazza r. Ann N Y Acad Sci. 1995 Jul 7;756:414-7. doi: 10.1111/j.1749-6632.1995.tb44549.x. Ann N Y Acad Sci. 1995. PMID: 7645861 No abstract available.

6

T-cell infiltration in polymyositis is characterized by coexpression of cytotoxic and T-cell-activating cytokine transcripts.

Andreetta F, Bernasconi P, Torchiana E, Baggi F, Cornelio F, Mantegazza R. Andreetta F, et al. Among authors: mantegazza r. Ann N Y Acad Sci. 1995 Jul 7;756:418-20. doi: 10.1111/j.1749-6632.1995.tb44550.x. Ann N Y Acad Sci. 1995. PMID: 7645862 No abstract available.

7

Cellular aspects of myositis.

Mantegazza R, Bernasconi P. Mantegazza R, et al. Curr Opin Rheumatol. 1994 Nov;6(6):568-74. doi: 10.1097/00002281-199411000-00004. Curr Opin Rheumatol. 1994. PMID: 7865375 Review.

8

Very small dystrophin molecule in a family with a mild form of Becker dystrophy.

Morandi L, Mora M, Bernasconi P, Mantegazza R, Gebbia M, Balestrini MR, Cornelio F. Morandi L, et al. Among authors: mantegazza r. Neuromuscul Disord. 1993 Jan;3(1):65-70. doi: 10.1016/0960-8966(93)90043-j. Neuromuscul Disord. 1993. PMID: 8329891

9

Analysis of T cell receptor repertoire of muscle-infiltrating T lymphocytes in polymyositis. Restricted V alpha/beta rearrangements may indicate antigen-driven selection.

Mantegazza R, Andreetta F, Bernasconi P, Baggi F, Oksenberg JR, Simoncini O, Mora M, Cornelio F, Steinman L. Mantegazza R, et al. J Clin Invest. 1993 Jun;91(6):2880-6. doi: 10.1172/JCI116533. J Clin Invest. 1993. PMID: 8514895 Free PMC article.

10

Dystrophin characterization in BMD patients: correlation of abnormal protein with clinical phenotype.

Morandi L, Mora M, Confalonieri V, Barresi R, Di Blasi C, Brugnoni R, Bernasconi P, Mantegazza R, Dworzak F, Antozzi C, et al. Morandi L, et al. Among authors: mantegazza r. J Neurol Sci. 1995 Oct;132(2):146-55. doi: 10.1016/0022-510x(95)00147-t. J Neurol Sci. 1995. PMID: 8543940 Clinical Trial.

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