Shy ME - Search Results

1

Diagnosis and new treatments in genetic neuropathies.

Reilly MM, Shy ME. Reilly MM, et al. Among authors: shy me. J Neurol Neurosurg Psychiatry. 2009 Dec;80(12):1304-14. doi: 10.1136/jnnp.2008.158295. J Neurol Neurosurg Psychiatry. 2009. PMID: 19917815 Review.

2

Hereditary motor and sensory neuropathies: a biological perspective.

Shy ME, Garbern JY, Kamholz J. Shy ME, et al. Lancet Neurol. 2002 Jun;1(2):110-8. doi: 10.1016/s1474-4422(02)00042-x. Lancet Neurol. 2002. PMID: 12849515 Review.

3

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

4

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.

5

Dispersion of compound muscle action potential in hereditary neuropathies and chronic inflammatory demyelinating polyneuropathy.

Stanton M, Pannoni V, Lewis RA, Logigian EL, Naguib D, Shy ME, Cleland J, Herrmann DN. Stanton M, et al. Among authors: shy me. Muscle Nerve. 2006 Oct;34(4):417-22. doi: 10.1002/mus.20600. Muscle Nerve. 2006. PMID: 16823858

6

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

7

Charcot-Marie-Tooth neuropathies: diagnosis and management.

Jani-Acsadi A, Krajewski K, Shy ME. Jani-Acsadi A, et al. Among authors: shy me. Semin Neurol. 2008 Apr;28(2):185-94. doi: 10.1055/s-2008-1062264. Semin Neurol. 2008. PMID: 18351520 Review.

8

PMP22 expression in dermal nerve myelin from patients with CMT1A.

Katona I, Wu X, Feely SM, Sottile S, Siskind CE, Miller LJ, Shy ME, Li J. Katona I, et al. Among authors: shy me. Brain. 2009 Jul;132(Pt 7):1734-40. doi: 10.1093/brain/awp113. Epub 2009 May 15. Brain. 2009. PMID: 19447823 Free PMC article.

9

168th ENMC International Workshop: outcome measures and clinical trials in Charcot-Marie-Tooth disease (CMT).

Reilly MM, Shy ME, Muntoni F, Pareyson D. Reilly MM, et al. Among authors: shy me. Neuromuscul Disord. 2010 Dec;20(12):839-46. doi: 10.1016/j.nmd.2010.08.001. Epub 2010 Sep 17. Neuromuscul Disord. 2010. PMID: 20850975 No abstract available.

10

Charcot-Marie-Tooth disease subtypes and genetic testing strategies.

Saporta AS, Sottile SL, Miller LJ, Feely SM, Siskind CE, Shy ME. Saporta AS, et al. Among authors: shy me. Ann Neurol. 2011 Jan;69(1):22-33. doi: 10.1002/ana.22166. Ann Neurol. 2011. PMID: 21280073 Free PMC article.

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