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English
Impairment of neuromuscular transmission in a subgroup of migraine patients
scientific article published on 01 December 1999
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10612640
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10612640%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
title
Impairment of neuromuscular transmission in a subgroup of migraine patients
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10612640
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10612640%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
main subject
migraine
1 reference
based on heuristic
inferred from title
author name string
A Ambrosini
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10612640
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10612640%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
A M de Noordhout
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10612640
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10612640%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
G Alagona
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10612640
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10612640%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
F Dalpozzo
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10612640
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10612640%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
J Schoenen
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10612640
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10612640%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
language of work or name
English
0 references
publication date
1 December 1999
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10612640
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10612640%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
published in
Neuroscience Letters
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10612640
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10612640%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
volume
276
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10612640
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10612640%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
issue
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10612640
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10612640%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
page(s)
201-203
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10612640
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10612640%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
cites work
Mutations in the Cacnl1a4 calcium channel gene are associated with seizures, cerebellar degeneration, and ataxia in tottering and leaner mutant mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0304-3940%2899%2900820-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Absence epilepsy in tottering mutant mice is associated with calcium channel defects
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0304-3940%2899%2900820-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0304-3940%2899%2900820-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial typical migraine: linkage to chromosome 19p13 and evidence for genetic heterogeneity.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0304-3940%2899%2900820-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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/10.1016%2FS0304-3940%2899%2900820-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
AAEM minimonograph #25: single-fiber electromyography
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0304-3940%2899%2900820-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The study of normal and abnormal neuromuscular transmission with single fibre electromyography
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0304-3940%2899%2900820-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel omega-conopeptide for the presynaptic localization of calcium channels at the mammalian neuromuscular junction
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0304-3940%2899%2900820-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Migraine, ataxia and epilepsy: a challenging spectrum of genetically determined calcium channelopathies. Dutch Migraine Genetics Research Group
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0304-3940%2899%2900820-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0304-3940(99)00820-4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10612640
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10612640%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
PubMed publication ID
10612640
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10612640
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10612640%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
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