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English
Arthrogryposis multiplex congenita
scientific article published on 01 October 1998
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9840670
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9840670%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
review article
1 reference
stated in
Europe PubMed Central
title
Arthrogryposis multiplex congenita
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9840670
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9840670%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
author name string
N Gordon
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9840670
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9840670%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
publication date
1 October 1998
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9840670
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9840670%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
published in
Brain and Development
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9840670
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9840670%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
volume
20
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9840670
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9840670%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
issue
7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9840670
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9840670%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
page(s)
507-511
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9840670
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9840670%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
cites work
Arthrogryposis Multiplex Congenita
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900037-0
retrieved
7 January 2021
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Epileptic seizures, arthrogryposis, and migrational brain disorders: a syndrome?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900037-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lethal arthrogryposis in Finland--a clinico-pathological study of 83 cases during thirteen years
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900037-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neurogenic arthrogryposis multiplex congenita: clinical and MRI findings.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900037-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Olivo-ponto-cerebellar atrophy with muscular atrophy, joint contractures and pulmonary hypoplasia of prenatal onset
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900037-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital progressive muscular dystrophy of the Fukuyama type - clinical, genetic and pathological considerations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900037-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Arthrogryposis multiplex congenita. Review with comment
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900037-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lethal arthrogryposis with anterior horn cell disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900037-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Arthrogryposis due to infantile neuronal degeneration associated with deletion of the SMNT gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900037-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Arthrogryposis multiplex congenita: spectrum of pathologic changes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900037-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital non-progressive peripheral neuropathy with arthrogryposis multiplex
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900037-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Arthrogryposis multiplex congenita due to congenital myasthenic syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900037-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Arthrogryposis Multiplex Congenita due to Congenital Myasthenia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900037-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Association of arthrogryposis multiplex congenita with maternal antibodies inhibiting fetal acetylcholine receptor function
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900037-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lethal congenital muscular dystrophy with arthrogryposis multiplex congenita: three new cases and review of the literature
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900037-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deficiency of a skeletal muscle isoform of α-actinin (α-actinin-3) in merosin-positive congenital muscular dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900037-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ragged-red fibers and complex I deficiency in a neonate With arthrogryposis congenita
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900037-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A revised and extended classification of the distal arthrogryposes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900037-0
retrieved
7 January 2021
based on heuristic
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Arthrogryposis multiplex congenita: a report of two cases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900037-0
retrieved
7 January 2021
based on heuristic
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The diagnostic management of newborns with congenital contractures: a nosologic study of 75 cases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900037-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Part I. Amyoplasia: A common, sporadic condition with congenital contractures
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900037-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prenatal findings in generalized amyoplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900037-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Camptodactyly, cleft palate, and club foot. A syndrome showing the autosomal-dominant pattern of inheritance
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900037-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Extending the spectrum of distal arthrogryposis.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900037-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Distal arthrogryposis type 1: clinical analysis of a large kindred
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900037-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The spectrum of arthrogryposis in 33 chinese children.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900037-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Arthrogryposis multiplex congenita; feeding, language and other health problems
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0387-7604%2898%2900037-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0387-7604(98)00037-0
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9840670
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9840670%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
PubMed publication ID
9840670
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9840670
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9840670%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
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