Luigetti M - Search Results

1

Long-term treatment of hereditary transthyretin amyloidosis with patisiran: multicentre, real-world experience in Italy.

Gentile L, Mazzeo A, Briani C, Casagrande S, De Luca M, Fabrizi GM, Gagliardi C, Gemelli C, Forcina F, Grandis M, Guglielmino V, Iabichella G, Leonardi L, Lozza A, Manganelli F, Mussinelli R, My F, Occhipinti G, Fenu S, Russo M, Romano A, Salvalaggio A, Tagliapietra M, Tozza S, Palladini G, Obici L, Luigetti M. Gentile L, et al. Among authors: luigetti m. Neurol Sci. 2024 Sep;45(9):4563-4571. doi: 10.1007/s10072-024-07494-9. Epub 2024 Apr 16. Neurol Sci. 2024. PMID: 38622453 Free PMC article.

2

A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype.

Luigetti M, Fabrizi GM, Madia F, Ferrarini M, Conte A, Del Grande A, Tasca G, Tonali PA, Sabatelli M. Luigetti M, et al. J Neurol Sci. 2010 Nov 15;298(1-2):114-7. doi: 10.1016/j.jns.2010.09.008. Epub 2010 Sep 25. J Neurol Sci. 2010. PMID: 20870250

3

Clinical, electrophysiological and pathological findings of a patient with CMT2 due to the p.Ala738Val mitofusin 2 mutation.

Luigetti M, Fabrizi GM, Taioli F, Conte A, Del Grande A, Sabatelli M. Luigetti M, et al. J Neurol Sci. 2011 Aug 15;307(1-2):168-70. doi: 10.1016/j.jns.2011.04.025. Epub 2011 May 20. J Neurol Sci. 2011. PMID: 21601224

4

Sural nerve pathology in ALS patients: a single-centre experience.

Luigetti M, Conte A, Del Grande A, Bisogni G, Romano A, Sabatelli M. Luigetti M, et al. Neurol Sci. 2012 Oct;33(5):1095-9. doi: 10.1007/s10072-011-0909-5. Epub 2011 Dec 28. Neurol Sci. 2012. PMID: 22203334

5

Luigetti M, Conte A, Del Grande A, Bisogni G, Madia F, Lo Monaco M, Laurenti L, Obici L, Merlini G, Sabatelli M. Luigetti M, et al. Neurol Sci. 2013 Jul;34(7):1057-63. doi: 10.1007/s10072-012-1105-y. Epub 2012 May 17. Neurol Sci. 2013. PMID: 22592564

6

Inherited neuropathies and deafness caused by a PMP22 point mutation: a case report and a review of the literature.

Luigetti M, Zollino M, Conti G, Romano A, Sabatelli M. Luigetti M, et al. Neurol Sci. 2013 Sep;34(9):1705-7. doi: 10.1007/s10072-012-1277-5. Epub 2012 Dec 24. Neurol Sci. 2013. PMID: 23263778 Review. No abstract available.

7

Influence of comorbidities on the phenotype of patients affected by Charcot-Marie-Tooth neuropathy type 1A.

Ursino G, Alberti MA, Grandis M, Reni L, Pareyson D, Bellone E, Gemelli C, Sabatelli M, Pisciotta C, Luigetti M, Santoro L, Massollo L, Schenone A. Ursino G, et al. Among authors: luigetti m. Neuromuscul Disord. 2013 Nov;23(11):902-6. doi: 10.1016/j.nmd.2013.07.002. Epub 2013 Jul 23. Neuromuscul Disord. 2013. PMID: 23891256

8

Heterogeneity of root and nerve ultrasound pattern in CIDP patients.

Padua L, Granata G, Sabatelli M, Inghilleri M, Lucchetta M, Luigetti M, Coraci D, Martinoli C, Briani C. Padua L, et al. Among authors: luigetti m. Clin Neurophysiol. 2014 Jan;125(1):160-5. doi: 10.1016/j.clinph.2013.07.023. Epub 2013 Oct 5. Clin Neurophysiol. 2014. PMID: 24099922

9

Ultrasound evaluation in transthyretin-related amyloid neuropathy.

Granata G, Luigetti M, Coraci D, Del Grande A, Romano A, Bisogni G, Bramanti P, Rossini PM, Sabatelli M, Padua L. Granata G, et al. Among authors: luigetti m. Muscle Nerve. 2014 Sep;50(3):372-6. doi: 10.1002/mus.24168. Epub 2014 Jun 16. Muscle Nerve. 2014. PMID: 24395461

10

Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: a single-centre experience.

Luigetti M, Del Grande A, Conte A, Lo Monaco M, Bisogni G, Romano A, Zollino M, Rossini PM, Sabatelli M. Luigetti M, et al. J Neurol Sci. 2014 Jun 15;341(1-2):46-50. doi: 10.1016/j.jns.2014.03.046. Epub 2014 Mar 31. J Neurol Sci. 2014. PMID: 24726093

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