Nerve Conduction Abnormalities and Neuromyotonia in Genetically Engineered Mouse Models of Human Hereditary Neuropathies (Q47671993)

4 February 2018

title

Nerve Conduction Abnormalities and Neuromyotonia in Genetically Engineered Mouse Models of Human Hereditary Neuropathies (English)

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4 February 2018

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Klaus V Toyka

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Jürgen Zielasek

series ordinal

object named as

Jürgen Zielasek

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4 February 2018

language of work or name

English

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publication date

1 October 1999

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Annals of the New York Academy of Sciences

published in

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volume

883

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issue

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4 February 2018

page(s)

310-320

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Genetically determined neuropathies

cites work

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https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08593.X

Animal models for inherited peripheral neuropathies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08593.X

Construction of a mouse model of Charcot-Marie-Tooth disease type 1A by pronuclear injection of human YAC DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08593.X

Mouse P0 gene disruption leads to hypomyelination, abnormal expression of recognition molecules, and degeneration of myelin and axons.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08593.X

Defective propagation of signals generated by sympathetic nerve stimulation in the liver of connexin32-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08593.X

Hereditary neuromyotonia: a mouse model associated with deficiency or increased gene dosage of the PMP22 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08593.X

Trembler mouse carries a point mutation in a myelin gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08593.X

A leucine-to-proline mutation in the putative first transmembrane domain of the 22-kDa peripheral myelin protein in the trembler-J mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08593.X

Hereditary demyelinating neuropathy in the Trembler mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08593.X

Refractory period, conduction of trains of impulses, and effect of temperature on conduction in chronic hypertrophic neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08593.X

A SYNDROME OF CONTINUOUS MUSCLE-FIBRE ACTIVITY

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08593.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08593.X

AAEM minimonograph #44: diseases associated with excess motor unit activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08593.X

Hyperexcitability of motor and sensory neurons in neuromyotonia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08593.X

Hereditary motor-sensory neuropathy and movement disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1999.TB08593.X

10.1111/J.1749-6632.1999.TB08593.X

21 January 2018

Identifiers

DOI

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4 February 2018

release_dxfcqqtdvrddbich2t4m3r2xha

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/dxfcqqtdvrddbich2t4m3r2xha

mapped directly with Wikidata item

24 November 2022

based on heuristic

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4 February 2018