Stancanelli C - Search Results

1

Psychosocial impact of sport activity in neuromuscular disorders.

Vita GL, Stancanelli C, La Foresta S, Faraone C, Sframeli M, Ferrero A, Fattore C, Galbo R, Ferraro M, Ricci G, Cotti Piccinelli S, Pizzighello S, Filosto M, Martinuzzi A, Padua L, Trimarchi G, Siciliano G, Mongini T, Lombardo ME, Berardinelli A, Vita G. Vita GL, et al. Among authors: stancanelli c. Neurol Sci. 2020 Sep;41(9):2561-2567. doi: 10.1007/s10072-020-04345-1. Epub 2020 Apr 4. Neurol Sci. 2020. PMID: 32246354

2

Genetic neuromuscular disorders: living the era of a therapeutic revolution. Part 1: peripheral neuropathies.

Vita G, Vita GL, Stancanelli C, Gentile L, Russo M, Mazzeo A. Vita G, et al. Among authors: stancanelli c. Neurol Sci. 2019 Apr;40(4):661-669. doi: 10.1007/s10072-019-03778-7. Epub 2019 Mar 1. Neurol Sci. 2019. PMID: 30847674 Review.

3

Unilateral hyperhidrosis as persistently isolated feature of syringomyelia and Arnold Chiari type 1.

Stancanelli C, Mazzeo A, Gentile L, Vita G. Stancanelli C, et al. Neurol Sci. 2018 Sep;39(9):1607-1608. doi: 10.1007/s10072-018-3403-5. Epub 2018 Apr 10. Neurol Sci. 2018. PMID: 29637451 No abstract available.

4

Parenteral nutrition improves nutritional status, autonomic symptoms and quality of life in transthyretin amyloid polyneuropathy.

Russo M, Vita GL, Stancanelli C, Mazzeo A, Vita G, Messina S. Russo M, et al. Among authors: stancanelli c. Neuromuscul Disord. 2016 Jun;26(6):374-7. doi: 10.1016/j.nmd.2016.03.006. Epub 2016 Mar 30. Neuromuscul Disord. 2016. PMID: 27132122

5

Phenotypic variability of TTR Val122Ile mutation: a Caucasian patient with axonal neuropathy and normal heart.

Stancanelli C, Gentile L, Di Bella G, Minutoli F, Russo M, Vita G, Mazzeo A. Stancanelli C, et al. Neurol Sci. 2017 Mar;38(3):525-526. doi: 10.1007/s10072-016-2767-7. Epub 2016 Nov 12. Neurol Sci. 2017. PMID: 27838833 No abstract available.

6

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: stancanelli c. 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.

7

Charcot-Marie-Tooth 2F: phenotypic presentation of the Arg136Leu HSP27 mutation in a multigenerational family.

Stancanelli C, Fabrizi GM, Ferrarini M, Cavallaro T, Taioli F, Di Leo R, Russo M, Gentile L, Toscano A, Vita G, Mazzeo A. Stancanelli C, et al. Neurol Sci. 2015 Jun;36(6):1003-6. doi: 10.1007/s10072-014-2050-8. Epub 2014 Dec 30. Neurol Sci. 2015. PMID: 25547330

8

The Spinal Muscular Atrophy Health Index: Italian validation of a disease-specific outcome measure.

Sansone VA, Pirola A, Lizio A, Greco LC, Coratti G, Casiraghi J, Pane M, Pera MC, Italiano C, Messina S, Pozzi S, Sframeli M, D'Amico A, Bertini E, Bruno C, Mauro L, Salmin F, Stancanelli C, Pedemonte M, Albamonte E, Zizzi C, Heatwole C, Mercuri E; ISMAC group. Sansone VA, et al. Among authors: stancanelli c. Neuromuscul Disord. 2021 May;31(5):409-418. doi: 10.1016/j.nmd.2021.02.006. Epub 2021 Feb 9. Neuromuscul Disord. 2021. PMID: 33773884

9

Autonomic involvement in subacute and chronic immune-mediated neuropathies.

Mazzeo A, Stancanelli C, Di Leo R, Vita G. Mazzeo A, et al. Among authors: stancanelli c. Autoimmune Dis. 2013;2013:549465. doi: 10.1155/2013/549465. Epub 2013 Jun 18. Autoimmune Dis. 2013. PMID: 23853716 Free PMC article.

10

Transthyretin-Related Familial Amyloid Polyneuropathy (TTR-FAP): A Single-Center Experience in Sicily, an Italian Endemic Area.

Mazzeo A, Russo M, Di Bella G, Minutoli F, Stancanelli C, Gentile L, Baldari S, Carerj S, Toscano A, Vita G. Mazzeo A, et al. Among authors: stancanelli c. J Neuromuscul Dis. 2015 Jul 22;2(s2):S39-S48. doi: 10.3233/JND-150091. J Neuromuscul Dis. 2015. PMID: 27858761 Free PMC article.

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