(Q73365717)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10639608%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

title

Unusual electrophysiological findings in X-linked dominant Charcot-Marie-Tooth disease (English)

1 reference

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3 November 2019

author name string

A Gutierrez

1

1 reference

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3 November 2019

J D England

2

1 reference

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3 November 2019

A J Sumner

3

1 reference

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3 November 2019

S Ferer

4

1 reference

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3 November 2019

L E Warner

5

1 reference

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3 November 2019

J R Lupski

6

1 reference

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3 November 2019

C A Garcia

7

1 reference

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3 November 2019

publication date

1 February 2000

1 reference

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3 November 2019

1 reference

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3 November 2019

volume

23

1 reference

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3 November 2019

issue

2

1 reference

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3 November 2019

page(s)

182-188

1 reference

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

3 November 2019

cites work

1 reference

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X-linked Charcot-Marie-Tooth disease with connexin 32 mutations: clinical and electrophysiologic study.

21 January 2018

1 reference

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

21 January 2018

1 reference

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Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies

21 January 2018

1 reference

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Screening of dominantly inherited Charcot-Marie-Tooth neuropathies

21 January 2018

1 reference

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Distal accentuation of conduction slowing in polyneuropathy associated with antibodies to myelin-associated glycoprotein and sulphated glucuronyl paragloboside

21 January 2018

1 reference

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The electrodiagnostic distinctions between chronic familial and acquired demyelinative neuropathies

21 January 2018

1 reference

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DNA duplication associated with Charcot-Marie-Tooth disease type 1A

21 January 2018

1 reference

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Intermediate nerve conduction velocities define X-linked Charcot-Marie-Tooth neuropathy families

21 January 2018

1 reference

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Changes in permeability caused by connexin 32 mutations underlie X-linked Charcot-Marie-Tooth disease

21 January 2018

1 reference

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Connexin 32 mutations from X-linked Charcot-Marie-Tooth disease patients: functional defects and dominant negative effects

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-4598%28200002%2923%3A2%3C182%3A%3AAID-MUS6%3E3.0.CO%3B2-W

Genetically determined neuropathies

21 January 2018

1 reference

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Hereditary motor and sensory neuropathy, X-linked: a half century follow-up

21 January 2018

1 reference

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Demyelinating X-linked Charcot-Marie-Tooth disease: unusual electrophysiological findings

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291097-4598%28200002%2923%3A2%3C182%3A%3AAID-MUS6%3E3.0.CO%3B2-W

10.1002/(SICI)1097-4598(200002)23:2<182::AID-MUS6>3.0.CO;2-W

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10639608%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

1 reference