(Q43585274)

24 November 2017

Familial continuous motor unit activity and epilepsy (English)

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24 November 2017

1

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24 November 2017

Avoni P

2

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24 November 2017

Baruzzi A

series ordinal

3

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24 November 2017

Di Stasi V

series ordinal

4

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24 November 2017

Montagna P

series ordinal

5

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24 November 2017

1 May 2001

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24 November 2017

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24 November 2017

24

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24 November 2017

5

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24 November 2017

630-633

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A dominantly inherited syndrome with continuous motor neuron discharges.

24 November 2017

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Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1

21 January 2018

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Normocalcemic tetany abolished by calcium infusion

21 January 2018

1 reference

Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability

21 January 2018

1 reference

A critical survey of stiff-man syndrome

21 January 2018

1 reference

Neuromyotonia in hereditary motor neuropathy

21 January 2018

1 reference

A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns

21 January 2018

1 reference

A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy

21 January 2018

1 reference

Hereditary form of sustained muscle activity of peripheral nerve origin causing generalized myokymia and muscle stiffness

21 January 2018

1 reference

Hereditary continuous muscle fiber activity

21 January 2018

1 reference

Hereditary myokymia and periodic ataxia

21 January 2018

1 reference

Neuronal type of Charcot-Marie-Tooth disease with a syndrome of continuous motor unit activity

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/MUS.1048

1 reference

24 November 2017

1 reference