Shy ME - Search Results

1

Phenotype expression in women with CMT1X.

Siskind CE, Murphy SM, Ovens R, Polke J, Reilly MM, Shy ME. Siskind CE, et al. Among authors: shy me. J Peripher Nerv Syst. 2011 Jun;16(2):102-7. doi: 10.1111/j.1529-8027.2011.00332.x. J Peripher Nerv Syst. 2011. PMID: 21692908

2

Neurological dysfunction and axonal degeneration in Charcot-Marie-Tooth disease type 1A.

Krajewski KM, Lewis RA, Fuerst DR, Turansky C, Hinderer SR, Garbern J, Kamholz J, Shy ME. Krajewski KM, et al. Among authors: shy me. Brain. 2000 Jul;123 ( Pt 7):1516-27. doi: 10.1093/brain/123.7.1516. Brain. 2000. PMID: 10869062 Clinical Trial.

3

Motor unit number estimate of distal and proximal muscles in Charcot-Marie-Tooth disease.

Lewis RA, Li J, Fuerst DR, Shy ME, Krajewski K. Lewis RA, et al. Among authors: shy me. Muscle Nerve. 2003 Aug;28(2):161-7. doi: 10.1002/mus.10419. Muscle Nerve. 2003. PMID: 12872319 Clinical Trial.

4

Loss-of-function phenotype of hereditary neuropathy with liability to pressure palsies.

Li J, Krajewski K, Lewis RA, Shy ME. Li J, et al. Among authors: shy me. Muscle Nerve. 2004 Feb;29(2):205-10. doi: 10.1002/mus.10521. Muscle Nerve. 2004. PMID: 14755484

5

Skin biopsies in myelin-related neuropathies: bringing molecular pathology to the bedside.

Li J, Bai Y, Ghandour K, Qin P, Grandis M, Trostinskaia A, Ianakova E, Wu X, Schenone A, Vallat JM, Kupsky WJ, Hatfield J, Shy ME. Li J, et al. Among authors: shy me. Brain. 2005 May;128(Pt 5):1168-77. doi: 10.1093/brain/awh483. Epub 2005 Mar 17. Brain. 2005. PMID: 15774502

6

Reliability and validity of the CMT neuropathy score as a measure of disability.

Shy ME, Blake J, Krajewski K, Fuerst DR, Laura M, Hahn AF, Li J, Lewis RA, Reilly M. Shy ME, et al. Neurology. 2005 Apr 12;64(7):1209-14. doi: 10.1212/01.WNL.0000156517.00615.A3. Neurology. 2005. PMID: 15824348 Clinical Trial.

7

T118M PMP22 mutation causes partial loss of function and HNPP-like neuropathy.

Shy ME, Scavina MT, Clark A, Krajewski KM, Li J, Kamholz J, Kolodny E, Szigeti K, Fischer RA, Saifi GM, Scherer SS, Lupski JR. Shy ME, et al. Ann Neurol. 2006 Feb;59(2):358-64. doi: 10.1002/ana.20777. Ann Neurol. 2006. PMID: 16437560

8

CMT1X phenotypes represent loss of GJB1 gene function.

Shy ME, Siskind C, Swan ER, Krajewski KM, Doherty T, Fuerst DR, Ainsworth PJ, Lewis RA, Scherer SS, Hahn AF. Shy ME, et al. Neurology. 2007 Mar 13;68(11):849-55. doi: 10.1212/01.wnl.0000256709.08271.4d. Neurology. 2007. PMID: 17353473

9

Neuropathy progression in Charcot-Marie-Tooth disease type 1A.

Shy ME, Chen L, Swan ER, Taube R, Krajewski KM, Herrmann D, Lewis RA, McDermott MP. Shy ME, et al. Neurology. 2008 Jan 29;70(5):378-83. doi: 10.1212/01.wnl.0000297553.36441.ce. Neurology. 2008. PMID: 18227419

10

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: shy me. 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

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