Merosin-deficient congenital muscular dystrophy with cerebral white matter changes: a clue to its diagnosis beyond infancy. (Q42416006)

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scientific article published on 6 March 2014

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English	Merosin-deficient congenital muscular dystrophy with cerebral white matter changes: a clue to its diagnosis beyond infancy.	scientific article published on 6 March 2014

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instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PMC publication ID

3948005

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24604798%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 March 2020

case report

0 references

title

Merosin-deficient congenital muscular dystrophy with cerebral white matter changes: a clue to its diagnosis beyond infancy (English)

1 reference

stated in

Europe PubMed Central

PMC publication ID

3948005

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24604798%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 March 2020

main subject

congenital disorder

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congenital muscular dystrophy

1 reference

based on heuristic

inferred from title

infancy stage

1 reference

based on heuristic

inferred from title

author

Suneel C Mundkur

series ordinal

3

1 reference

stated in

Europe PubMed Central

PMC publication ID

3948005

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24604798%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 March 2020

author name string

Sandeep Kumar

series ordinal

1

1 reference

stated in

Europe PubMed Central

PMC publication ID

3948005

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24604798%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 March 2020

Shrikiran Aroor

series ordinal

2

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stated in

Europe PubMed Central

PMC publication ID

3948005

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24604798%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 March 2020

Maneesh Kumar

series ordinal

4

1 reference

stated in

Europe PubMed Central

PMC publication ID

3948005

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24604798%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 March 2020

publication date

6 March 2014

1 reference

stated in

Europe PubMed Central

PMC publication ID

3948005

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24604798%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 March 2020

published in

BMJ case reports

1 reference

stated in

Europe PubMed Central

PMC publication ID

3948005

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24604798%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 March 2020

volume

2014

1 reference

stated in

Europe PubMed Central

PMC publication ID

3948005

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24604798%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 March 2020

cites work

The congenital muscular dystrophies in 2004: a century of exciting progress

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3948005

retrieved

28 May 2018

The expanding phenotype of laminin alpha2 chain (merosin) abnormalities: case series and review

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3948005

retrieved

28 May 2018

Update on genetic disorders affecting white matter

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3948005

retrieved

28 May 2018

MR imaging findings in children with merosin-deficient congenital muscular dystrophy

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3948005

retrieved

28 May 2018

Merosin promotes cell attachment and neurite outgrowth and is a component of the neurite-promoting factor of RN22 schwannoma cells

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3948005

retrieved

28 May 2018

Congenital muscular dystrophy: use of brain MR imaging findings to predict merosin deficiency

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3948005

retrieved

16 August 2018

Late onset muscular dystrophy with cerebral white matter changes due to partial merosin deficiency

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3948005

retrieved

16 August 2018

Brain alterations in the classical form of congenital muscular dystrophy. Clinical and neuroimaging follow-up of 12 cases and correlation with the expression of merosin in muscle

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3948005

retrieved

16 August 2018

Congenital muscular dystrophy with primary laminin alpha2 (merosin) deficiency presenting as inflammatory myopathy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/24604798

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differential diagnosis of congenital muscular dystrophies

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/24604798

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The muscular dystrophies

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/24604798

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Merosin-deficient congenital muscular dystrophy, autosomal recessive (MDC1A, MIM#156225, LAMA2 gene coding for alpha2 chain of laminin)

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/24604798

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

White matter abnormalities in congenital muscular dystrophy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/24604798

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of merosin in the normal human brain: implications for congenital muscular dystrophy with merosin deficiency

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/24604798

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1136/BCR-2013-202684

1 reference

stated in

Europe PubMed Central

PMC publication ID

3948005

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24604798%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 March 2020

PMC publication ID

3948005

1 reference

stated in

Europe PubMed Central

PMC publication ID

3948005

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24604798%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 March 2020

PubMed publication ID

24604798

1 reference

stated in

Europe PubMed Central

PMC publication ID

3948005

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24604798%20AND%20SRC:MED&resulttype=core&format=json

retrieved

9 March 2020

 

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