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English
Familial concordance of brain magnetic resonance imaging changes in congenital muscular dystrophy
scientific article published on 01 May 1995
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7633188
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7633188%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
title
Familial concordance of brain magnetic resonance imaging changes in congenital muscular dystrophy
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7633188
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7633188%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
main subject
congenital muscular dystrophy
1 reference
based on heuristic
inferred from title
author name string
J. Philpot
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7633188
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7633188
retrieved
25 June 2024
H. Topaloglu
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7633188
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7633188
retrieved
25 June 2024
J. Pennock
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7633188
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7633188
retrieved
25 June 2024
V. Dubowitz
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7633188
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7633188
retrieved
25 June 2024
language of work or name
English
1 reference
stated in
National Center for Biotechnology Information
PubMed publication ID
7633188
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=7633188
retrieved
25 June 2024
publication date
1 May 1995
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7633188
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7633188%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
full work available at URL
https://api.elsevier.com/content/article/PII:096089669400047D?httpAccept=text/xml
1 reference
stated in
Crossref
DOI
10.1016/0960-8966(94)00047-D
reference URL
https://api.crossref.org/works/10.1016/0960-8966(94)00047-D
retrieved
25 June 2024
https://api.elsevier.com/content/article/PII:096089669400047D?httpAccept=text/plain
1 reference
stated in
Crossref
DOI
10.1016/0960-8966(94)00047-D
reference URL
https://api.crossref.org/works/10.1016/0960-8966(94)00047-D
retrieved
25 June 2024
published in
Neuromuscular Disorders
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7633188
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7633188%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
volume
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7633188
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7633188%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
issue
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7633188
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7633188%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
page(s)
227-231
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7633188
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7633188%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
cites work
Congenital progressive muscular dystrophy of the Fukuyama type - clinical, genetic and pathological considerations
series ordinal
2
1 reference
stated in
Crossref
DOI
10.1016/0960-8966(94)00047-D
reference URL
https://api.crossref.org/works/10.1016/0960-8966(94)00047-D
retrieved
25 June 2024
Diagnostic criteria for Walker-Warburg syndrome
series ordinal
4
1 reference
stated in
Crossref
DOI
10.1016/0960-8966(94)00047-D
reference URL
https://api.crossref.org/works/10.1016/0960-8966(94)00047-D
retrieved
25 June 2024
Congenital muscular dystrophy and cerebral CT scan anomalies. Results of a collaborative study of the Société de Neurologie Infantile
series ordinal
6
1 reference
stated in
Crossref
DOI
10.1016/0960-8966(94)00047-D
reference URL
https://api.crossref.org/works/10.1016/0960-8966(94)00047-D
retrieved
25 June 2024
Congenital muscular dystrophy with cerebral involvement--report of a case of "occidental type cerebromuscular dystrophy"?
series ordinal
7
1 reference
stated in
Crossref
DOI
10.1016/0960-8966(94)00047-D
reference URL
https://api.crossref.org/works/10.1016/0960-8966(94)00047-D
retrieved
25 June 2024
Occidental type cerebromuscular dystrophy: a report of eleven cases
series ordinal
9
1 reference
stated in
Crossref
DOI
10.1016/0960-8966(94)00047-D
reference URL
https://api.crossref.org/works/10.1016/0960-8966(94)00047-D
retrieved
25 June 2024
Congenital muscular dystrophy with abnormal radiographic myelin pattern
series ordinal
10
1 reference
stated in
Crossref
DOI
10.1016/0960-8966(94)00047-D
reference URL
https://api.crossref.org/works/10.1016/0960-8966(94)00047-D
retrieved
25 June 2024
Classification of the cerebro-oculo-muscular syndrome(s). Commentary to Kimura's paper (pp. 182-91)
series ordinal
11
1 reference
stated in
Crossref
DOI
10.1016/0960-8966(94)00047-D
reference URL
https://api.crossref.org/works/10.1016/0960-8966(94)00047-D
retrieved
25 June 2024
Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31-33
series ordinal
12
1 reference
stated in
Crossref
DOI
10.1016/0960-8966(94)00047-D
reference URL
https://api.crossref.org/works/10.1016/0960-8966(94)00047-D
retrieved
25 June 2024
Congenital muscular dystrophy with merosin deficiency
series ordinal
13
1 reference
stated in
Crossref
DOI
10.1016/0960-8966(94)00047-D
reference URL
https://api.crossref.org/works/10.1016/0960-8966(94)00047-D
retrieved
25 June 2024
Laminin variants: why, where and when?
series ordinal
14
1 reference
stated in
Crossref
DOI
10.1016/0960-8966(94)00047-D
reference URL
https://api.crossref.org/works/10.1016/0960-8966(94)00047-D
retrieved
25 June 2024
Identifiers
DOI
10.1016/0960-8966(94)00047-D
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7633188
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7633188%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
PubMed publication ID
7633188
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7633188
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7633188%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
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