(Q58193689)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15654555%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

title

LGI1 gene mutation screening in sporadic partial epilepsy with auditory features (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15654555%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15654555%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

Bruno Dallapiccola

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15654555%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

author name string

E Flex

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15654555%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

C Di Bonaventura

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15654555%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

S Douzgou

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15654555%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

G Egeo

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15654555%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

J Fattouch

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15654555%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

M Manfredi

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15654555%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

A T Giallonardo

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15654555%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

publication date

1 January 2005

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15654555%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15654555%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

volume

252

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15654555%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15654555%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

page(s)

62-66

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15654555%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s00415-005-0599-0

7 January 2020

exact match

0 references

cites work

Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features

1 reference

12 December 2020

LGI1 is mutated in familial temporal lobe epilepsy characterized by aphasic seizures

1 reference

12 December 2020

Epilepsy with auditory features: a LGI1 gene mutation suggests a loss-of-function mechanism

1 reference

12 December 2020

Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy

1 reference

12 December 2020

Autosomal dominant partial epilepsy with auditory features: description of a new family.

1 reference

12 December 2020

Familial temporal lobe epilepsy with aphasic seizures and linkage to chromosome 10q22-q24.

1 reference

12 December 2020

Novel LGI1 mutation in a family with autosomal dominant partial epilepsy with auditory features

1 reference

12 December 2020

Four new families with autosomal dominant partial epilepsy with auditory features: clinical description and linkage to chromosome 10q24.

1 reference

12 December 2020

Localization of a gene for partial epilepsy to chromosome 10q

1 reference

12 December 2020

Autosomal dominant partial epilepsy with auditory features: defining the phenotype

1 reference

12 December 2020

Autosomal dominant lateral temporal epilepsy: clinical and genetic study of a large Basque pedigree linked to chromosome 10q.

1 reference

12 December 2020

10.1007/S00415-005-0599-0

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15654555%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

1 reference