(Q30495660)

13 November 2017

Central visual, acoustic, and motor pathway involvement in a Charcot-Marie-Tooth family with an Asn205Ser mutation in the connexin 32 gene (English)

1 reference

13 November 2017

Bähr M

1

1 reference

13 November 2017

Andres F

2

1 reference

13 November 2017

Timmerman V

3

1 reference

13 November 2017

Nelis ME

4

1 reference

13 November 2017

Van Broeckhoven C

5

1 reference

13 November 2017

Dichgans J

6

1 reference

13 November 2017

language of work or name

English

0 references

publication date

1 February 1999

1 reference

Journal of Neurology, Neurosurgery and Psychiatry

13 November 2017

1 reference

13 November 2017

66

1 reference

13 November 2017

2

1 reference

13 November 2017

202-206

1 reference

Charcot-Marie-Tooth disease and related peripheral neuropathies

13 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1736220

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1736220

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1736220

Slowing of central conduction in X-linked Charcot-Marie-Tooth neuropathy shown by brain stem auditory evoked responses

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1736220

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1736220

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1736220

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1736220

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1736220

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1736220

Peripheral and central sensory nerve conduction in Charcot-Marie-Tooth disease and comparison with Friedreich's ataxia.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1736220

X-linked dominant hereditary motor and sensory neuropathy

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1736220

Gap junctions: new tools, new answers, new questions

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1736220

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1736220

Oligodendrocytes express gap junction proteins connexin32 and connexin45.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1736220

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

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1736220

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

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1736220

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

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10071100

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10071100

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10071100

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JNNP.66.2.202

1 reference

13 November 2017

1 reference

13 November 2017

1 reference