Gentile L - Search Results

1

Diagnostic utility of Sudoscan for detecting bortezomib-induced painful neuropathy: a study on 18 patients with multiple myeloma.

Allegra A, Rizzo V, Innao V, Alibrandi A, Mazzeo A, Leanza R, Terranova C, Gentile L, Girlanda P, Allegra AG, Alonci A, Musolino C. Allegra A, et al. Among authors: gentile l. Arch Med Sci. 2021 Jan 11;18(3):696-703. doi: 10.5114/aoms/114269. eCollection 2022. Arch Med Sci. 2021. PMID: 35591819 Free PMC article.

2

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. Among authors: gentile l. 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

3

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: gentile l. 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

4

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. 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.

5

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. Among authors: gentile l. Neurol Sci. 2015 Jun;36(6):1003-6. doi: 10.1007/s10072-014-2050-8. Epub 2014 Dec 30. Neurol Sci. 2015. PMID: 25547330

6

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. Among authors: gentile l. 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.

7

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: gentile l. J Neuromuscul Dis. 2015 Jul 22;2(s2):S39-S48. doi: 10.3233/JND-150091. J Neuromuscul Dis. 2015. PMID: 27858761 Free PMC article.

8

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. Among authors: gentile l. 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.

9

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: gentile l. 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.

10

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: gentile l. 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.

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