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Congenital myasthenic syndromes
scientific article published on 01 May 1994
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scholarly article
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stated in
Europe PubMed Central
PubMed ID
8041349
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8041349%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
review article
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Europe PubMed Central
title
Congenital myasthenic syndromes
(English)
1 reference
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Europe PubMed Central
PubMed ID
8041349
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8041349%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
author name string
Engel AG
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
8041349
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8041349%20AND%20SRC:MED&resulttype=core&format=json
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23 October 2019
publication date
1 May 1994
1 reference
stated in
Europe PubMed Central
PubMed ID
8041349
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8041349%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
published in
Neurologic Clinics
1 reference
stated in
Europe PubMed Central
PubMed ID
8041349
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8041349%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
volume
12
1 reference
stated in
Europe PubMed Central
PubMed ID
8041349
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8041349%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
issue
2
1 reference
stated in
Europe PubMed Central
PubMed ID
8041349
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8041349%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
page(s)
401-437
1 reference
stated in
Europe PubMed Central
PubMed ID
8041349
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8041349%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
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Familial neuromuscular disease with type 1 fiber hypoplasia, tubular aggregates, cardiomyopathy, and myasthenic features
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Congenital myasthenic syndromes: I. Deficiency and short open-time of the acetylcholine receptor.
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Familial infantile myasthenia gravis. Report of three cases with follow-up until adult life
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Congenital myasthenia associated with facial malformations in Iraqi and Iranian Jews. A new genetic syndrome
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7 January 2021
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Congenital myasthenia gravis
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Crossref
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7 January 2021
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A study of desensitization of acetylcholine receptors using nerve-released transmitter in the frog
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Analysis of anticholinesterase-induced neuromuscular transmission failure.
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THE SLOW CHANNEL SYNDROME
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1 reference
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7 January 2021
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1 reference
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7 January 2021
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inferred from DOI database lookup
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1 reference
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7 January 2021
based on heuristic
inferred from DOI database lookup
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1 reference
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reference URL
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7 January 2021
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inferred from DOI database lookup
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1 reference
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reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
A myasthenic syndrome with congenital paucity of secondary synaptic clefts: CPSC Syndrome
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Paucity of secondary synaptic clefts in a case of congenital myasthenia with multiple contractures: ultrastructural morphology of a developmental disorder
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
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1 reference
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7 January 2021
based on heuristic
inferred from DOI database lookup
Effects of calcium on the conductance change of the end-plate membrane during the action of transmitter
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930104-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital myasthenic syndromes: II. Syndrome attributed to abnormal interaction of acetylcholine with its receptor
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
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1 reference
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reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital myasthenia: end-plate acetylcholine receptors and electrophysiology in five cases
1 reference
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Crossref
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7 January 2021
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inferred from DOI database lookup
Clinical and experimental observations in patients with congenital myasthenic syndromes
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7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital myasthenic syndrome associated with paucity of synaptic vesicles and reduced quantal release
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reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930104-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital paucity of secondary synaptic clefts (CPSC) syndrome in 2 adult sibs.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930104-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
The effect of prednisolone on the rat phrenic nerve-diaphragm preparation treated with hemicholinium
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reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Thymectomy for myasthenia gravis in children
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930104-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0733-8619(18)30104-X
1 reference
stated in
Europe PubMed Central
PubMed ID
8041349
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8041349%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
PubMed ID
8041349
1 reference
stated in
Europe PubMed Central
PubMed ID
8041349
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8041349%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
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