(Q46555569)

English

Autosomal dominant nocturnal frontal lobe epilepsy and mild memory impairment associated with CHRNB2 mutation I312M in the neuronal nicotinic acetylcholine receptor

scientific article published on 4 June 2008

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/18534914

Autosomal dominant nocturnal frontal lobe epilepsy and mild memory impairment associated with CHRNB2 mutation I312M in the neuronal nicotinic acetylcholine receptor (English)

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/18534914

autosomal dominant nocturnal frontal lobe epilepsy

0 references

author name string

Yong-Won Cho

1

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/18534914

Sang-Doe Yi

2

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/18534914

Jeong-Geun Lim

3

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/18534914

Dae-Kwang Kim

4

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/18534914

Gholam K Motamedi

5

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/18534914

publication date

4 June 2008

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/18534914

Epilepsy Behavior

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/18534914

13

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/18534914

2

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/18534914

361-365

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/18534914

From nocturnal paroxysmal dystonia to nocturnal frontal lobe epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEBEH.2008.04.017

7 January 2021

Movement disorders in sleep: guidelines for differentiating epileptic from non-epileptic motor phenomena arising from sleep

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEBEH.2008.04.017

7 January 2021

Interobserver reliability of video recording in the diagnosis of nocturnal frontal lobe seizures.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEBEH.2008.04.017

7 January 2021

The CHRNB2 mutation I312M is associated with epilepsy and distinct memory deficits

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEBEH.2008.04.017

7 January 2021

Autosomal dominant nocturnal frontal lobe epilepsy with a mutation in the CHRNB2 gene

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEBEH.2008.04.017

7 January 2021

Hyperperfusion of anterior cingulate gyrus in a case of paroxysmal nocturnal dystonia.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEBEH.2008.04.017

7 January 2021

A Korean Kindred With Autosomal Dominant Nocturnal Frontal Lobe Epilepsy and Mental Retardation

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEBEH.2008.04.017

7 January 2021

Identifiers

10.1016/J.YEBEH.2008.04.017

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/18534914

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

23 December 2017

http://europepmc.org/abstract/MED/18534914

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