Fischbeck KH - Search Results

1

A unique mutation in connexin32 associated with severe, early onset CMTX in a heterozygous female.

Lin GS, Glass JD, Shumas S, Scherer SS, Fischbeck KH. Lin GS, et al. Among authors: fischbeck kh. Ann N Y Acad Sci. 1999 Sep 14;883:481-4. Ann N Y Acad Sci. 1999. PMID: 10586279 No abstract available.

2

X-linked Charcot-Marie-Tooth Disease and Connexin32.

Fischbeck KH, Abel A, Lin GS, Scherer SS. Fischbeck KH, et al. Ann N Y Acad Sci. 1999 Oct;883(1):36-41. doi: 10.1111/j.1749-6632.1999.tb08564.x. Ann N Y Acad Sci. 1999. PMID: 29086942

3

A Unique Mutation in Connexin32 Associated with Severe, Early Onset CMTX in a Heterozygous Female.

Lin GS, Glass JD, Shumas S, Scherer SS, Fischbeck KH. Lin GS, et al. Among authors: fischbeck kh. Ann N Y Acad Sci. 1999 Oct;883(1):481-484. doi: 10.1111/j.1749-6632.1999.tb08616.x. Ann N Y Acad Sci. 1999. PMID: 29086962 No abstract available.

4

Severe neuropathy with leaky connexin32 hemichannels.

Liang GS, de Miguel M, Gómez-Hernández JM, Glass JD, Scherer SS, Mintz M, Barrio LC, Fischbeck KH. Liang GS, et al. Among authors: fischbeck kh. Ann Neurol. 2005 May;57(5):749-54. doi: 10.1002/ana.20459. Ann Neurol. 2005. PMID: 15852376

5

Connexin32 and X-linked Charcot-Marie-Tooth disease.

Fischbeck KH, Deschênes SM, Bone LJ, Scherer SS. Fischbeck KH, et al. Cold Spring Harb Symp Quant Biol. 1996;61:673-7. Cold Spring Harb Symp Quant Biol. 1996. PMID: 9246493 Review. No abstract available.

6

Connexin32 and X-linked Charcot-Marie-Tooth disease.

Bone LJ, Deschênes SM, Balice-Gordon RJ, Fischbeck KH, Scherer SS. Bone LJ, et al. Among authors: fischbeck kh. Neurobiol Dis. 1997;4(3-4):221-30. doi: 10.1006/nbdi.1997.0152. Neurobiol Dis. 1997. PMID: 9361298 Free article. Review.

7

Altered trafficking of mutant connexin32.

Deschênes SM, Walcott JL, Wexler TL, Scherer SS, Fischbeck KH. Deschênes SM, et al. Among authors: fischbeck kh. J Neurosci. 1997 Dec 1;17(23):9077-84. doi: 10.1523/JNEUROSCI.17-23-09077.1997. J Neurosci. 1997. PMID: 9364054 Free PMC article.

8

X-linked Charcot-Marie-Tooth disease and connexin32.

Fischbeck KH, Abel A, Lin GS, Scherer SS. Fischbeck KH, et al. Ann N Y Acad Sci. 1999 Sep 14;883:36-41. Ann N Y Acad Sci. 1999. PMID: 10586227 Review.

9

Connexin32-null mice develop demyelinating peripheral neuropathy.

Scherer SS, Xu YT, Nelles E, Fischbeck K, Willecke K, Bone LJ. Scherer SS, et al. Glia. 1998 Sep;24(1):8-20. doi: 10.1002/(sici)1098-1136(199809)24:1<8::aid-glia2>3.0.co;2-3. Glia. 1998. PMID: 9700485

10

Transgenic expression of human connexin32 in myelinating Schwann cells prevents demyelination in connexin32-null mice.

Scherer SS, Xu YT, Messing A, Willecke K, Fischbeck KH, Jeng LJ. Scherer SS, et al. Among authors: fischbeck kh. J Neurosci. 2005 Feb 9;25(6):1550-9. doi: 10.1523/JNEUROSCI.3082-04.2005. J Neurosci. 2005. PMID: 15703409 Free PMC article.

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