Partial epilepsy: chinks in the armour (Q71990849)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647788%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

title

Partial epilepsy: chinks in the armour (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647788%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

S. G. Ryan

1 reference

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13 July 2024

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=7647788

13 July 2024

publication date

1 May 1995

1 reference

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full work available at URL

22 October 2019

http://www.nature.com/articles/ng0595-4

1 reference

https://api.crossref.org/works/10.1038/NG0595-4

http://www.nature.com/articles/ng0595-4.pdf

13 July 2024

file format

Portable Document Format

1 reference

https://api.crossref.org/works/10.1038/NG0595-4

13 July 2024

1 reference

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22 October 2019

volume

1 reference

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22 October 2019

issue

1 reference

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22 October 2019

page(s)

4-6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647788%20AND%20SRC:MED&resulttype=core&format=json

Proposal for revised classification of epilepsies and epileptic syndromes. Commission on Classification and Terminology of the International League Against Epilepsy

22 October 2019

cites work

1 reference

7 January 2021

Juvenile myoclonic epilepsy (JME) may be linked to the BF and HLA loci on human chromosome 6

1 reference

7 January 2021

Confirmation of linkage between juvenile myoclonic epilepsy locus and the HLA region of chromosome 6.

1 reference

7 January 2021

Benign epilepsy of childhood with centrotemporal EEG foci: a genetic study

1 reference

7 January 2021

Progressive myoclonus epilepsies: specific causes and diagnosis

1 reference

7 January 2021

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

1 reference

7 January 2021

Localization of a gene for partial epilepsy to chromosome 10q

1 reference

7 January 2021

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

1 reference

7 January 2021

Benign familial neonatal convulsions linked to genetic markers on chromosome 20.

1 reference

7 January 2021

A nonsense mutation in the α4 subunit of the nicotinic acetylcholine receptor (CHRNA4) cosegregates with 20q-linked benign neonatal familial convulsions (EBNI)

1 reference

7 January 2021

Epilepsy Research. Supplement

201

JL Noebels

1991

1 reference

https://api.crossref.org/works/10.1038/NG0595-4

13 July 2024

Identifiers

DOI

10.1038/NG0595-4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647788%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

1 reference

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