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Items: 19

1.

Charcot-Marie-Tooth disease and related peripheral neuropathies.

De Jonghe P, Timmerman V, Nelis E, Martin JJ, Van Broeckhoven C.

J Peripher Nerv Syst. 1997;2(4):370-87. Review.

PMID:
10975746
2.

Oligodendrocytes express gap junction proteins connexin32 and connexin45.

Dermietzel R, Farooq M, Kessler JA, Althaus H, Hertzberg EL, Spray DC.

Glia. 1997 Jun;20(2):101-14.

PMID:
9179595
3.

Connexin32 gene mutations in X-linked dominant Charcot-Marie-Tooth disease (CMTX1).

Janssen EA, Kemp S, Hensels GW, Sie OG, de Die-Smulders CE, Hoogendijk JE, de Visser M, Bolhuis PA.

Hum Genet. 1997 Apr;99(4):501-5.

PMID:
9099841
4.

Connexin32 in oligodendrocytes and association with myelinated fibers in mouse and rat brain.

Li J, Hertzberg EL, Nagy JI.

J Comp Neurol. 1997 Mar 24;379(4):571-91.

PMID:
9067844
5.

Mutation analysis of the connexin 32 (Cx32) gene in Charcot-Marie-Tooth neuropathy type 1: identification of five new mutations.

Nelis E, Simokovic S, Timmerman V, Löfgren A, Backhovens H, De Jonghe P, Martin JJ, Van Broeckhoven C.

Hum Mutat. 1997;9(1):47-52. No abstract available.

PMID:
8990008
6.

Gap junctions in the adult cerebral cortex: regional differences in their distribution and cellular expression of connexins.

Nadarajah B, Thomaidou D, Evans WH, Parnavelas JG.

J Comp Neurol. 1996 Dec 9;376(2):326-42.

PMID:
8951647
7.

The pathology of charcot-marie-tooth disease and related disorders.

Thomas PK, King RH, Small JR, Robertson AM.

Neuropathol Appl Neurobiol. 1996 Aug;22(4):269-84. Review.

PMID:
8875461
8.
9.

Connexin mutations in X-linked Charcot-Marie-Tooth disease.

Bergoffen J, Scherer SS, Wang S, Scott MO, Bone LJ, Paul DL, Chen K, Lensch MW, Chance PF, Fischbeck KH.

Science. 1993 Dec 24;262(5142):2039-42.

PMID:
8266101
10.

Null mutations of connexin32 in patients with X-linked Charcot-Marie-Tooth disease.

Bruzzone R, White TW, Scherer SS, Fischbeck KH, Paul DL.

Neuron. 1994 Nov;13(5):1253-60.

PMID:
7946361
11.

Charcot-Marie-Tooth neuropathies: from clinical description to molecular genetics.

Ionasescu VV.

Muscle Nerve. 1995 Mar;18(3):267-75. Review.

PMID:
7870103
12.

Molecular genetics of Charcot-Marie-Tooth disease and related neuropathies.

Chance PF, Fischbeck KH.

Hum Mol Genet. 1994;3 Spec No:1503-7. Review.

PMID:
7849745
13.

Gap junctions in the brain: where, what type, how many and why?

Dermietzel R, Spray DC.

Trends Neurosci. 1993 May;16(5):186-92. Review.

PMID:
7685944
14.

Genetic aspects of hereditary motor and sensory neuropathy (types I and II).

Harding AE, Thomas PK.

J Med Genet. 1980 Oct;17(5):329-36. No abstract available.

15.
16.

Visual evoked potential abnormalities in Charcot-Marie-Tooth disease and comparison with Friedreich's ataxia.

Carroll WM, Jones SJ, Halliday AM.

J Neurol Sci. 1983 Sep;61(1):123-33.

PMID:
6631447
17.

X-linked dominant hereditary motor and sensory neuropathy.

Hahn AF, Brown WF, Koopman WJ, Feasby TE.

Brain. 1990 Oct;113 ( Pt 5):1511-25.

PMID:
2245309
18.

Gap junctions: new tools, new answers, new questions.

Bennett MV, Barrio LC, Bargiello TA, Spray DC, Hertzberg E, Sáez JC.

Neuron. 1991 Mar;6(3):305-20. Review. No abstract available.

PMID:
1848077
19.

F response and somatosensory and brainstem auditory evoked potential studies in HMSN type I and II.

Scaioli V, Pareyson D, Avanzini G, Sghirlanzoni A.

J Neurol Neurosurg Psychiatry. 1992 Nov;55(11):1027-31.

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