Russo M - Search Results

1

6MWT performance correlates with peripheral neuropathy but not with cardiac involvement in patients with hereditary transthyretin amyloidosis (hATTR).

Vita GL, Stancanelli C, Gentile L, Barcellona C, Russo M, Di Bella G, Vita G, Mazzeo A. Vita GL, et al. Among authors: russo m. Neuromuscul Disord. 2019 Mar;29(3):213-220. doi: 10.1016/j.nmd.2018.11.002. Epub 2018 Nov 14. Neuromuscul Disord. 2019. PMID: 30718023 Free article.

2

Expression of transglutaminase 2 does not differentiate focal myositis from generalized inflammatory myopathies.

Macaione V, Aguennouz M, Mazzeo A, De Pasquale MG, Russo M, Toscano A, De Luca G, Di Giorgio RM, Vita G, Rodolico C. Macaione V, et al. Among authors: russo m. Acta Neurol Scand. 2008 Jun;117(6):393-8. doi: 10.1111/j.1600-0404.2007.00957.x. Epub 2007 Nov 14. Acta Neurol Scand. 2008. PMID: 18005224

3

Psychosocial impact of presymptomatic genetic testing for transthyretin amyloidotic polyneuropathy.

Graceffa A, Russo M, Vita GL, Toscano A, Dattola R, Messina C, Vita G, Mazzeo A. Graceffa A, et al. Among authors: russo m. Neuromuscul Disord. 2009 Jan;19(1):44-8. doi: 10.1016/j.nmd.2008.09.017. Epub 2008 Dec 11. Neuromuscul Disord. 2009. PMID: 19084401

4

Flavocoxid counteracts muscle necrosis and improves functional properties in mdx mice: a comparison study with methylprednisolone.

Messina S, Bitto A, Aguennouz M, Mazzeo A, Migliorato A, Polito F, Irrera N, Altavilla D, Vita GL, Russo M, Naro A, De Pasquale MG, Rizzuto E, Musarò A, Squadrito F, Vita G. Messina S, et al. Among authors: russo m. Exp Neurol. 2009 Dec;220(2):349-58. doi: 10.1016/j.expneurol.2009.09.015. Epub 2009 Sep 25. Exp Neurol. 2009. PMID: 19786019

5

MRI of cardiac involvement in transthyretin familial amyloid polyneuropathy.

Di Bella G, Minutoli F, Mazzeo A, Vita G, Oreto G, Carerj S, Anfuso C, Russo M, Gaeta M. Di Bella G, et al. Among authors: russo m. AJR Am J Roentgenol. 2010 Dec;195(6):W394-9. doi: 10.2214/AJR.09.3721. AJR Am J Roentgenol. 2010. PMID: 21098170

6

Variable phenotypes are associated with PMP22 missense mutations.

Russo M, Laurá M, Polke JM, Davis MB, Blake J, Brandner S, Hughes RA, Houlden H, Bennett DL, Lunn MP, Reilly MM. Russo M, et al. Neuromuscul Disord. 2011 Feb;21(2):106-14. doi: 10.1016/j.nmd.2010.11.011. Epub 2010 Dec 30. Neuromuscul Disord. 2011. PMID: 21194947

7

Subacute inflammatory demyelinating polyneuropathy disclosed by massive nerve root enhancement in CMT1A.

Mazzeo A, Stancanelli C, Russo M, Granata F, Gentile L, Di Leo R, Vita G, Nobile-Orazio E, Toscano A. Mazzeo A, et al. Among authors: russo m. Muscle Nerve. 2012 Mar;45(3):451-2. doi: 10.1002/mus.22260. Epub 2011 Dec 15. Muscle Nerve. 2012. PMID: 22173780 No abstract available.

8

Transthyretin-related familial amyloidotic polyneuropathy: description of a cohort of patients with Leu64 mutation and late onset.

Russo M, Mazzeo A, Stancanelli C, Di Leo R, Gentile L, Di Bella G, Minutoli F, Baldari S, Vita G. Russo M, et al. J Peripher Nerv Syst. 2012 Dec;17(4):385-90. doi: 10.1111/j.1529-8027.2012.00436.x. J Peripher Nerv Syst. 2012. PMID: 23279339

9

Unusual features of central nervous system involvement in CMTX associated with a novel mutation of GJB1 gene.

Stancanelli C, Taioli F, Testi S, Fabrizi GM, Arena MG, Granata F, Russo M, Gentile L, Vita G, Mazzeo A. Stancanelli C, et al. Among authors: russo m. J Peripher Nerv Syst. 2012 Dec;17(4):407-11. doi: 10.1111/j.1529-8027.2012.00439.x. J Peripher Nerv Syst. 2012. PMID: 23279342

10

Considerable post-partum worsening in a patient with CMT2E.

Gentile L, Taioli F, Fabrizi GM, Russo M, Stancanelli C, Mazzeo A. Gentile L, et al. Among authors: russo m. Neurol Sci. 2013 Oct;34(10):1813-4. doi: 10.1007/s10072-013-1296-x. Epub 2013 Feb 15. Neurol Sci. 2013. PMID: 23412702 No abstract available.

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