Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q73573252)
Watch
English
Merosin-positive congenital muscular dystrophy with mental retardation and cataracts: a new entity in two families
scientific article published on 01 January 1997
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10728208
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10728208%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
title
Merosin-positive congenital muscular dystrophy with mental retardation and cataracts: a new entity in two families
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10728208
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10728208%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
main subject
congenital muscular dystrophy
1 reference
based on heuristic
inferred from title
author name string
H Topaloğlu
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10728208
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10728208%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
M Yetük
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10728208
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10728208%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
B Talim
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10728208
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10728208%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
Z Akçören
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10728208
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10728208%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
M Cağlar
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10728208
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10728208%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
publication date
1 January 1997
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10728208
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10728208%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
published in
European Journal of Paediatric Neurology
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10728208
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10728208%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
volume
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10728208
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10728208%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
issue
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10728208
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10728208%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
page(s)
127-131
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10728208
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10728208%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
cites work
Congenital Muscular Dystrophy: A Clinico-Pathological and Follow-Up Study of 15 Patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1090-3798%2897%2980045-1
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%2FS1090-3798%2897%2980045-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital muscular dystrophy: a clinicopathologic report of 24 cases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1090-3798%2897%2980045-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Diagnostic criteria for Walker-Warburg syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1090-3798%2897%2980045-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital muscular dystrophy associated with familial junctional epidermolysis bullosa letalis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1090-3798%2897%2980045-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A case of Ullrich's disease (Kongenitale, Atonisch-Sklerotische Muskeldystrophie)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1090-3798%2897%2980045-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lissencephaly and other malformations of cortical development: 1995 update
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1090-3798%2897%2980045-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lethal congenital muscular dystrophy in two sibs with arthrogryposis multiplex: new entity or variant of cobblestone lissencephaly syndrome?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1090-3798%2897%2980045-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31-33
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1090-3798%2897%2980045-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Abnormal localization of laminin subunits in muscular dystrophies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1090-3798%2897%2980045-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Muscle-eye-brain disease: a neuropathological study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1090-3798%2897%2980045-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Muscle-eye-brain disease and Fukuyama type congenital muscular dystrophy are not allelic
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1090-3798%2897%2980045-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Preserved merosin M-chain (or laminin-alpha 2) expression in skeletal muscle distinguishes Walker-Warburg syndrome from Fukuyama muscular dystrophy and merosin-deficient congenital muscular dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1090-3798%2897%2980045-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Laminin-alpha 2 chain (merosin M) is preserved in the Walker-Warburg syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1090-3798%2897%2980045-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Analysis of "pure" congenital muscular dystrophies in thirty-eight cases. How different is the classical type 1 from the occidental type cerebromuscular dystrophy?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1090-3798%2897%2980045-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial concordance of brain magnetic resonance imaging changes in congenital muscular dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1090-3798%2897%2980045-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Late onset muscular dystrophy with cerebral white matter changes due to partial merosin deficiency.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1090-3798%2897%2980045-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Somatosensory and visual evoked potentials in congenital muscular dystrophy: correlation with MRI changes and muscle merosin status
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1090-3798%2897%2980045-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Merosin-negative congenital muscular dystrophy associated with extensive brain abnormalities
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1090-3798%2897%2980045-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Merosin-negative congenital muscular dystrophy, occipital epilepsy with periodic spasms and focal cortical dysplasia. Report of three Italian cases in two families.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1090-3798%2897%2980045-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expression of laminin subunits in congenital muscular dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1090-3798%2897%2980045-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1090-3798%2897%2980045-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ocular findings in Fukuyama type congenital muscular dystrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1090-3798%2897%2980045-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cerebellar micropolygyria in Fukuyama congenital muscular dystrophy: observations in fetal and pediatric cases.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1090-3798%2897%2980045-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
MRI of the brain in muscle-eye-brain (MEB) disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1090-3798%2897%2980045-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ocular findings in muscle-eye-brain (MEB) disease: a follow-up study.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1090-3798%2897%2980045-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cerebellar ataxia, congenital cataracts, and retarded somatic and mental maturation. Report of cases of Marinesco-Sjogren syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1090-3798%2897%2980045-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neuropathy with lysosomal changes in Marinesco-Sjögren syndrome: fine structural findings in skeletal muscle and conjunctiva
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1090-3798%2897%2980045-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Muscle pathology in Marinesco-Sjogren syndrome: a unique ultrastructural feature
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1090-3798%2897%2980045-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital muscular dystrophy and cerebellar vermis agenesis in two brothers
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1090-3798%2897%2980045-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital Muscular Dystrophy with Cerebellar Atrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1090-3798%2897%2980045-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lethal congenital muscular dystrophy with cataracts and a minor brain anomaly: new entity or variant of Walker-Warburg syndrome?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1090-3798%2897%2980045-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S1090-3798(97)80045-1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10728208
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10728208%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
PubMed publication ID
10728208
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10728208
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10728208%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit