(Q33822321)

29 July 2017

1 reference

title

Electroclinical picture of autosomal dominant nocturnal frontal lobe epilepsy in a Japanese family (English)

1 reference

autosomal dominant nocturnal frontal lobe epilepsy

29 July 2017

0 references

author name string

Ito M

1

1 reference

29 July 2017

Kobayashi K

2

1 reference

29 July 2017

Fujii T

3

1 reference

29 July 2017

Okuno T

4

1 reference

29 July 2017

Hirose S

5

1 reference

29 July 2017

Iwata H

6

1 reference

29 July 2017

Mitsudome A

7

1 reference

29 July 2017

Kaneko S

8

1 reference

29 July 2017

1 January 2000

1 reference

29 July 2017

1 reference

29 July 2017

41

1 reference

29 July 2017

1

1 reference

29 July 2017

52-58

1 reference

Autosomal dominant frontal epilepsy misdiagnosed as sleep disorder

29 July 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.2000.TB01505.X

Epilepsies with single gene inheritance.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.2000.TB01505.X

Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q 13.2

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.2000.TB01505.X

Autosomal dominant nocturnal frontal-lobe epilepsy: genetic heterogeneity and evidence for a second locus at 15q24

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.2000.TB01505.X

A novel mutation of CHRNA4 responsible for autosomal dominant nocturnal frontal lobe epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.2000.TB01505.X

Exon-intron structure of the human neuronal nicotinic acetylcholine receptor alpha 4 subunit (CHRNA4)

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.2000.TB01505.X

A family with autosomal dominant nocturnal frontal lobe epilepsy and mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.2000.TB01505.X

A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.2000.TB01505.X

An insertion mutation of the CHRNA4 gene in a family with autosomal dominant nocturnal frontal lobe epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.2000.TB01505.X

An amino acid exchange in the second transmembrane segment of a neuronal nicotinic receptor causes partial epilepsy by altering its desensitization kinetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.2000.TB01505.X

Autosomal dominant nocturnal frontal lobe epilepsy. A video-polysomnographic and genetic appraisal of 40 patients and delineation of the epileptic syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.2000.TB01505.X

10.1111/J.1528-1157.2000.TB01505.X

21 January 2018

Identifiers

DOI

1 reference

29 July 2017

1 reference