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English
Partial epilepsy: chinks in the armour
scientific article published on 01 May 1995
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
7647788
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647788%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
title
Partial epilepsy: chinks in the armour
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
7647788
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647788%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
author name string
Ryan SG
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
7647788
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647788%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
publication date
1 May 1995
1 reference
stated in
Europe PubMed Central
PubMed ID
7647788
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647788%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
7647788
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647788%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
volume
10
1 reference
stated in
Europe PubMed Central
PubMed ID
7647788
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647788%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
page(s)
4-6
1 reference
stated in
Europe PubMed Central
PubMed ID
7647788
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647788%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
issue
1
1 reference
stated in
Europe PubMed Central
PubMed ID
7647788
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647788%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
exact match
https://scigraph.springernature.com/pub.10.1038/ng0595-4
0 references
cites work
Proposal for revised classification of epilepsies and epileptic syndromes. Commission on Classification and Terminology of the International League Against Epilepsy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0595-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Juvenile myoclonic epilepsy (JME) may be linked to the BF and HLA loci on human chromosome 6
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0595-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Confirmation of linkage between juvenile myoclonic epilepsy locus and the HLA region of chromosome 6.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0595-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Benign epilepsy of childhood with centrotemporal EEG foci: a genetic study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0595-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Progressive myoclonus epilepsies: specific causes and diagnosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0595-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0595-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Localization of a gene for partial epilepsy to chromosome 10q
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0595-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q 13.2
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0595-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Benign familial neonatal convulsions linked to genetic markers on chromosome 20.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0595-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A nonsense mutation in the alpha4 subunit of the nicotinic acetylcholine receptor (CHRNA4) cosegregates with 20q-linked benign neonatal familial convulsions (EBNI)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0595-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG0595-4
1 reference
stated in
Europe PubMed Central
PubMed ID
7647788
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647788%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
PubMed ID
7647788
1 reference
stated in
Europe PubMed Central
PubMed ID
7647788
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7647788%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
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