Severe myoclonic epilepsy of infancy: extended spectrum of GEFS+? (Q28211213)

From Wikidata

Jump to navigation Jump to search

scientific article (publication date: July 2001)

edit

Language	Label	Description	Also known as
English	Severe myoclonic epilepsy of infancy: extended spectrum of GEFS+?	scientific article (publication date: July 2001)

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11488881

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11488881%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

title

Severe myoclonic epilepsy of infancy: extended spectrum of GEFS+? (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11488881

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11488881%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

main subject

myoclonic epilepsy

1 reference

based on heuristic

inferred from title

author

William P Whitehouse

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11488881

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11488881%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

Samuel Berkovic

series ordinal

9

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11488881

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11488881%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

Ingrid Scheffer

series ordinal

10

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11488881

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11488881%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

author name string

R Singh

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11488881

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11488881%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

E Andermann

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11488881

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11488881%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

A S Harvey

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11488881

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11488881%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

D L Keene

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11488881

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11488881%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

M H Seni

series ordinal

6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11488881

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11488881%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

K M Crossland

series ordinal

7

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11488881

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11488881%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

F Andermann

series ordinal

8

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11488881

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11488881%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

language of work or name

English

0 references

publication date

1 July 2001

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11488881

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11488881%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

published in

Epilepsia

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11488881

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11488881%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

volume

42

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11488881

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11488881%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

issue

7

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11488881

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11488881%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

page(s)

837-844

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11488881

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11488881%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

cites work

Generalized epilepsy with febrile seizures plus. A genetic disorder with heterogeneous clinical phenotypes

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2001.042007837.X

retrieved

21 January 2018

A new locus for generalized epilepsy with febrile seizures plus maps to chromosome 2.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2001.042007837.X

retrieved

21 January 2018

A second locus for familial generalized epilepsy with febrile seizures plus maps to chromosome 2q21-q33.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2001.042007837.X

retrieved

21 January 2018

Identification of a new locus for generalized epilepsy with febrile seizures plus (GEFS+) on chromosome 2q24-q33.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2001.042007837.X

retrieved

21 January 2018

A locus for febrile seizures (FEB3) maps to chromosome 2q23-24

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2001.042007837.X

retrieved

21 January 2018

Radicals r'aging

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2001.042007837.X

retrieved

21 January 2018

Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2001.042007837.X

retrieved

21 January 2018

Severe idiopathic generalized epilepsy of infancy with generalized tonic-clonic seizures

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2001.042007837.X

retrieved

21 January 2018

Validation of a questionnaire for clinical seizure diagnosis

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2001.042007837.X

retrieved

21 January 2018

Clinical and neuropathologic findings in a case of severe myoclonic epilepsy of infancy

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2001.042007837.X

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2001.042007837.X

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2001.042007837.X

retrieved

21 January 2018

A potassium channel mutation in neonatal human epilepsy

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2001.042007837.X

retrieved

21 January 2018

A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2001.042007837.X

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2001.042007837.X

retrieved

21 January 2018

Ion channels and neurological disease: DNA based diagnosis is now possible, and ion channels may be important in common paroxysmal disorders

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2001.042007837.X

retrieved

21 January 2018

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2001.042007837.X

retrieved

21 January 2018

Identifiers

DOI

10.1046/J.1528-1157.2001.042007837.X

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11488881

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11488881%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

PubMed publication ID

11488881

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11488881

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11488881%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

ResearchGate publication ID

11854161

0 references

 

Sitelinks

Wikipedia(0 entries)

edit

Wikibooks(0 entries)

edit

Wikinews(0 entries)

edit

Wikiquote(0 entries)

edit

Wikisource(0 entries)

edit

Wikiversity(0 entries)

edit

Wikivoyage(0 entries)

edit

Wiktionary(0 entries)

edit

Multilingual sites(0 entries)

edit

Retrieved from "https://www.wikidata.org/w/index.php?title=Q28211213&oldid=1508659246"