Shy ME - Search Results

1

TRPV4 neuromuscular disease registry highlights bulbar, skeletal and proximal limb manifestations.

Kosmanopoulos G, Donohue JK, Hoke M, Thomas S, Peyton MA, Vo L, Crawford TO, Sadjadi R, Herrmann DN, Yum SW, Reilly MM, Scherer SS, Finkel RS, Lewis RA, Pareyson D, Pisciotta C, Walk D, Shy ME, Sumner CJ; Inherited Neuropathy Consortium; McCray BA. Kosmanopoulos G, et al. Among authors: shy me. Brain. 2024 Jun 25:awae201. doi: 10.1093/brain/awae201. Online ahead of print. Brain. 2024. PMID: 38917025

2

Mitogen-expanded Schwann cells retain the capacity to myelinate regenerating axons after transplantation into rat sciatic nerve.

Feltri ML, Scherer SS, Wrabetz L, Kamholz J, Shy ME. Feltri ML, et al. Among authors: shy me. Proc Natl Acad Sci U S A. 1992 Sep 15;89(18):8827-31. doi: 10.1073/pnas.89.18.8827. Proc Natl Acad Sci U S A. 1992. PMID: 1326765 Free PMC article.

3

An adenoviral vector can transfer lacZ expression into Schwann cells in culture and in sciatic nerve.

Shy ME, Tani M, Shi YJ, Whyatt SA, Chbihi T, Scherer SS, Kamholz J. Shy ME, et al. Ann Neurol. 1995 Sep;38(3):429-36. doi: 10.1002/ana.410380313. Ann Neurol. 1995. PMID: 7668829

4

Chronic inflammatory demyelinating polyneuropathy associated with malignant melanoma.

Bird SJ, Brown MJ, Shy ME, Scherer SS. Bird SJ, et al. Among authors: shy me. Neurology. 1996 Mar;46(3):822-4. doi: 10.1212/wnl.46.3.822. Neurology. 1996. PMID: 8618691

5

Axon-Schwann cell interactions regulate the expression of c-jun in Schwann cells.

Shy ME, Shi Y, Wrabetz L, Kamholz J, Scherer SS. Shy ME, et al. J Neurosci Res. 1996 Mar 1;43(5):511-25. doi: 10.1002/(SICI)1097-4547(19960301)43:5<511::AID-JNR1>3.0.CO;2-L. J Neurosci Res. 1996. PMID: 8833086

6

Heterozygous P0 knockout mice develop a peripheral neuropathy that resembles chronic inflammatory demyelinating polyneuropathy (CIDP).

Shy ME, Arroyo E, Sladky J, Menichella D, Jiang H, Xu W, Kamholz J, Scherer SS. Shy ME, et al. J Neuropathol Exp Neurol. 1997 Jul;56(7):811-21. J Neuropathol Exp Neurol. 1997. PMID: 9210878

7

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. Among authors: shy me. Ann N Y Acad Sci. 1999 Sep 14;883:477-80. Ann N Y Acad Sci. 1999. PMID: 10586278 No abstract available.

8

Electrodiagnostic findings in CMTX: a disorder of the Schwann cell and peripheral nerve myelin.

Lewis RA, Shy ME. Lewis RA, et al. Among authors: shy me. Ann N Y Acad Sci. 1999 Sep 14;883:504-7. Ann N Y Acad Sci. 1999. PMID: 10586285 No abstract available.

9

Charcot-Marie-Tooth disease type 1: molecular pathogenesis to gene therapy.

Kamholz J, Menichella D, Jani A, Garbern J, Lewis RA, Krajewski KM, Lilien J, Scherer SS, Shy ME. Kamholz J, et al. Among authors: shy me. Brain. 2000 Feb;123 ( Pt 2):222-33. doi: 10.1093/brain/123.2.222. Brain. 2000. PMID: 10648431 Review.

10

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.

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