Pareyson D - Search Results

1

Refining clinical trial inclusion criteria to optimize the standardized response mean of the CMTPedS.

Cornett KMD, Menezes MP, Bray P, Shy RR, Moroni I, Pagliano E, Pareyson D, Estilow T, Yum SW, Bhandari T, Muntoni F, Laura M, Reilly MM, Finkel RS, Eichinger KJ, Herrmann DN, Shy ME, Burns J; CMTPedS Study Group. Cornett KMD, et al. Among authors: pareyson d. Ann Clin Transl Neurol. 2020 Sep;7(9):1713-1715. doi: 10.1002/acn3.51145. Epub 2020 Aug 6. Ann Clin Transl Neurol. 2020. PMID: 32762141 Free PMC article.

2

Heterozygous null mutation in the P0 gene associated with mild Charcot-Marie-Tooth disease.

Pareyson D, Menichella D, Botti S, Sghirlanzoni A, Fallica E, Mora M, Ciano C, Shy ME, Taroni F. Pareyson D, et al. Ann N Y Acad Sci. 1999 Sep 14;883:477-80. Ann N Y Acad Sci. 1999. PMID: 10586278 No abstract available.

3

Childhood-onset multifocal motor neuropathy with conduction blocks.

Moroni I, Bugiani M, Ciano C, Bono R, Pareyson D. Moroni I, et al. Among authors: pareyson d. Neurology. 2006 Mar 28;66(6):922-4. doi: 10.1212/01.wnl.0000203346.25068.3f. Neurology. 2006. PMID: 16567714

4

136th ENMC International Workshop: Charcot-Marie-Tooth disease type 1A (CMT1A)8-10 April 2005, Naarden, The Netherlands.

Reilly MM, de Jonghe P, Pareyson D. Reilly MM, et al. Among authors: pareyson d. Neuromuscul Disord. 2006 Jun;16(6):396-402. doi: 10.1016/j.nmd.2006.03.008. Epub 2006 May 8. Neuromuscul Disord. 2006. PMID: 16684603 No abstract available.

5

Clinical and electrophysiological aspects of Charcot-Marie-Tooth disease.

Pareyson D, Scaioli V, Laurà M. Pareyson D, et al. Neuromolecular Med. 2006;8(1-2):3-22. doi: 10.1385/nmm:8:1-2:3. Neuromolecular Med. 2006. PMID: 16775364 Review.

6

Rapid progression of late onset axonal Charcot-Marie-Tooth disease associated with a novel MPZ mutation in the extracellular domain.

Laurà M, Milani M, Morbin M, Moggio M, Ripolone M, Jann S, Scaioli V, Taroni F, Pareyson D. Laurà M, et al. Among authors: pareyson d. J Neurol Neurosurg Psychiatry. 2007 Nov;78(11):1263-6. doi: 10.1136/jnnp.2006.112276. J Neurol Neurosurg Psychiatry. 2007. PMID: 17940173 Free PMC article.

7

The G389R mutation in the MAPT gene presenting as sporadic corticobasal syndrome.

Rossi G, Marelli C, Farina L, Laurà M, Maria Basile A, Ciano C, Tagliavini F, Pareyson D. Rossi G, et al. Among authors: pareyson d. Mov Disord. 2008 Apr 30;23(6):892-5. doi: 10.1002/mds.21970. Mov Disord. 2008. PMID: 18307268

8

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: pareyson d. 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

9

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: pareyson d. Neurol Sci. 2008 Jun;29(3):193-4. doi: 10.1007/s10072-008-0935-0. Epub 2008 Jul 9. Neurol Sci. 2008. PMID: 18612771

10

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: pareyson d. 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

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