Cavallaro T - Search Results

1

hATTR Pathology: Nerve Biopsy Results from Italian Referral Centers.

Luigetti M, Romozzi M, Bisogni G, Cardellini D, Cavallaro T, Di Paolantonio A, Fabrizi GM, Fenu S, Gentile L, Grandis M, Marucci G, Massucco S, Mazzeo A, Pareyson D, Romano A, Russo M, Schenone A, Tagliapietra M, Tozza S, Vita G, Sabatelli M. Luigetti M, et al. Among authors: cavallaro t. Brain Sci. 2020 Oct 26;10(11):780. doi: 10.3390/brainsci10110780. Brain Sci. 2020. PMID: 33114611 Free PMC article.

2

An unusual transthyretin gene missense mutation (TTR Phe33Val) linked to familial amyloidotic polyneuropathy.

Frigerio R, Fabrizi GM, Ferrarini M, Cavallaro T, Brighina L, Santoro P, Agostoni E, Cavaletti G, Rizzuto N, Ferrarese C. Frigerio R, et al. Among authors: cavallaro t. Amyloid. 2004 Jun;11(2):121-4. doi: 10.1080/13506120410001727767. Amyloid. 2004. PMID: 15478468

3

Charcot-Marie-Tooth disease type 2E, a disorder of the cytoskeleton.

Fabrizi GM, Cavallaro T, Angiari C, Cabrini I, Taioli F, Malerba G, Bertolasi L, Rizzuto N. Fabrizi GM, et al. Among authors: cavallaro t. Brain. 2007 Feb;130(Pt 2):394-403. doi: 10.1093/brain/awl284. Epub 2006 Oct 18. Brain. 2007. PMID: 17052987

4

A novel mutation of aprataxin associated with ataxia ocular apraxia type 1: phenotypical and genotypical characterization.

Ferrarini M, Squintani G, Cavallaro T, Ferrari S, Rizzuto N, Fabrizi GM. Ferrarini M, et al. Among authors: cavallaro t. J Neurol Sci. 2007 Sep 15;260(1-2):219-24. doi: 10.1016/j.jns.2007.05.015. Epub 2007 Jun 18. J Neurol Sci. 2007. PMID: 17572444

5

Correlation between clinical/neurophysiological findings and quality of life in Charcot-Marie-Tooth type 1A.

Padua L, Shy ME, Aprile I, Cavallaro T, Pareyson D, Quattrone A, Rizzuto N, Vita G, Tonali P, Schenone A. Padua L, et al. Among authors: cavallaro t. J Peripher Nerv Syst. 2008 Mar;13(1):64-70. doi: 10.1111/j.1529-8027.2008.00159.x. J Peripher Nerv Syst. 2008. PMID: 18346232

6

Charcot-Marie-Tooth and pain: correlations with neurophysiological, clinical, and disability findings.

Padua L, Cavallaro T, Pareyson D, Quattrone A, Vita G, Schenone A; Italian CMT QoL Study Group. Padua L, et al. Among authors: cavallaro t. Neurol Sci. 2008 Jun;29(3):193-4. doi: 10.1007/s10072-008-0935-0. Epub 2008 Jul 9. Neurol Sci. 2008. PMID: 18612771

7

Novel mutations in the GDAP1 gene in patients affected with early-onset axonal Charcot-Marie-Tooth type 4A.

Moroni I, Morbin M, Milani M, Ciano C, Bugiani M, Pagliano E, Cavallaro T, Pareyson D, Taroni F. Moroni I, et al. Among authors: cavallaro t. Neuromuscul Disord. 2009 Jul;19(7):476-80. doi: 10.1016/j.nmd.2009.04.014. Epub 2009 Jun 4. Neuromuscul Disord. 2009. PMID: 19500985

8

Inherited demyelinating neuropathies with micromutations of peripheral myelin protein 22 gene.

Taioli F, Cabrini I, Cavallaro T, Acler M, Fabrizi GM. Taioli F, et al. Among authors: cavallaro t. Brain. 2011 Feb;134(Pt 2):608-17. doi: 10.1093/brain/awq374. Epub 2011 Jan 19. Brain. 2011. PMID: 21252112

9

Vascular endothelial growth factor helps differentiate neuropathies in rare plasma cell dyscrasias.

Briani C, Fabrizi GM, Ruggero S, Torre CD, Ferrarini M, Campagnolo M, Cavallaro T, Ferrari S, Scarlato M, Taioli F, Adami F. Briani C, et al. Among authors: cavallaro t. Muscle Nerve. 2011 Feb;43(2):164-7. doi: 10.1002/mus.21872. Epub 2010 Nov 16. Muscle Nerve. 2011. PMID: 21254078

10

Ascorbic acid in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL and CMT-TRAUK): a double-blind randomised trial.

Pareyson D, Reilly MM, Schenone A, Fabrizi GM, Cavallaro T, Santoro L, Vita G, Quattrone A, Padua L, Gemignani F, Visioli F, Laurà M, Radice D, Calabrese D, Hughes RA, Solari A; CMT-TRIAAL; CMT-TRAUK groups. Pareyson D, et al. Among authors: cavallaro t. Lancet Neurol. 2011 Apr;10(4):320-8. doi: 10.1016/S1474-4422(11)70025-4. Lancet Neurol. 2011. PMID: 21393063 Free PMC article. Clinical Trial.

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