Familial West syndrome and dystonia caused by an Aristaless related homeobox gene mutation (Q81430287)

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scientific article published on 22 February 2005

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Language	Label	Description	Also known as
English	Familial West syndrome and dystonia caused by an Aristaless related homeobox gene mutation	scientific article published on 22 February 2005

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15726411

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15726411%20AND%20SRC:MED&resulttype=core&format=json

retrieved

8 January 2020

title

Familial West syndrome and dystonia caused by an Aristaless related homeobox gene mutation (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15726411

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15726411%20AND%20SRC:MED&resulttype=core&format=json

retrieved

8 January 2020

main subject

West syndrome

1 reference

based on heuristic

inferred from title

author

Jürgen Winkler

series ordinal

5

object named as

Jürgen Winkler

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15726411

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15726411%20AND%20SRC:MED&resulttype=core&format=json

retrieved

8 January 2020

author name string

Gabriele Wohlrab

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15726411

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15726411%20AND%20SRC:MED&resulttype=core&format=json

retrieved

8 January 2020

Goekhan Uyanik

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15726411

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15726411%20AND%20SRC:MED&resulttype=core&format=json

retrieved

8 January 2020

Claudia Gross

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15726411

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15726411%20AND%20SRC:MED&resulttype=core&format=json

retrieved

8 January 2020

Ute Hehr

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15726411

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15726411%20AND%20SRC:MED&resulttype=core&format=json

retrieved

8 January 2020

Bernhard Schmitt

series ordinal

6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15726411

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15726411%20AND%20SRC:MED&resulttype=core&format=json

retrieved

8 January 2020

Eugen Boltshauser

series ordinal

7

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15726411

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15726411%20AND%20SRC:MED&resulttype=core&format=json

retrieved

8 January 2020

publication date

22 February 2005

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15726411

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15726411%20AND%20SRC:MED&resulttype=core&format=json

retrieved

8 January 2020

published in

European Journal of Pediatrics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15726411

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15726411%20AND%20SRC:MED&resulttype=core&format=json

retrieved

8 January 2020

volume

164

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15726411

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15726411%20AND%20SRC:MED&resulttype=core&format=json

retrieved

8 January 2020

issue

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15726411

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15726411%20AND%20SRC:MED&resulttype=core&format=json

retrieved

8 January 2020

page(s)

326-328

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15726411

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15726411%20AND%20SRC:MED&resulttype=core&format=json

retrieved

8 January 2020

cites work

Infantile spasms, dystonia, and other X-linked phenotypes caused by mutations in Aristaless related homeobox gene, ARX

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15726411

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15726411

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ARX mutations in X-linked lissencephaly with abnormal genitalia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15726411

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Monogenic X-linked mental retardation: is it as frequent as currently estimated? The paradox of the ARX (Aristaless X) mutations.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15726411

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polyalanine expansion of ARX associated with cryptogenic West syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15726411

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neuroanatomical distribution of ARX in brain and its localisation in GABAergic neurons

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15726411

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mental retardation: X marks the spot.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15726411

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The ARX story (epilepsy, mental retardation, autism, and cerebral malformations): one gene leads to many phenotypes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15726411

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S00431-005-1622-2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15726411

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15726411%20AND%20SRC:MED&resulttype=core&format=json

retrieved

8 January 2020

Dimensions Publication ID

1000864177

0 references

PubMed publication ID

15726411

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15726411

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15726411%20AND%20SRC:MED&resulttype=core&format=json

retrieved

8 January 2020

 

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