The muscular dystrophies (Q33792223)

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Language	Label	Description	Also known as
English	The muscular dystrophies	scientific article

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9765171

retrieved

29 July 2017

review article

1 reference

stated in

Europe PubMed Central

title

The muscular dystrophies (English)

1 reference

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Europe PubMed Central

PubMed publication ID

9765171

retrieved

29 July 2017

author name string

A E Emery

series ordinal

1

1 reference

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Europe PubMed Central

PubMed publication ID

9765171

retrieved

29 July 2017

language of work or name

English

0 references

publication date

1 October 1998

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9765171

retrieved

29 July 2017

published in

The BMJ

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9765171

retrieved

29 July 2017

volume

317

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9765171

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29 July 2017

issue

7164

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9765171

retrieved

29 July 2017

page(s)

991-995

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Europe PubMed Central

PubMed publication ID

9765171

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29 July 2017

cites work

MUSCULAR DYSTROPHY: SOME RECENT ADVANCES IN KNOWLEDGE

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=1114045

retrieved

4 July 2018

Short GCG expansions in the PABP2 gene cause oculopharyngeal 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=1114045

retrieved

4 July 2018

Heart-specific localization of emerin: new insights into Emery-Dreifuss 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=1114045

retrieved

4 July 2018

Utrophin-dystrophin-deficient mice as a model for Duchenne 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=1114045

retrieved

4 July 2018

Dystrobrevin deficiency at the sarcolemma of patients with 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=1114045

retrieved

4 July 2018

Mutations in the sarcoglycan genes in patients with myopathy

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1114045

retrieved

4 July 2018

Advances in the molecular genetics of the limb-girdle type of autosomal recessive progressive 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=1114045

retrieved

4 July 2018

Development and validation of laboratory procedures for preimplantation diagnosis of Duchenne muscular dystrophy

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1114045

retrieved

4 July 2018

Autosomal dominant distal myopathy: linkage to chromosome 14.

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=1114045

retrieved

4 July 2018

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

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=1114045

retrieved

4 July 2018

The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal 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=1114045

retrieved

4 July 2018

Cloning of the breakpoint of an X;21 translocation associated with Duchenne 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=1114045

retrieved

4 July 2018

Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion

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=1114045

retrieved

4 July 2018

Location of facioscapulohumeral muscular dystrophy gene on chromosome 4.

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=1114045

retrieved

4 July 2018

On the classification, natural history and treatment of the myopathies

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=1114045

retrieved

30 October 2018

Germline mosaicism and Duchenne muscular dystrophy mutations

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=1114045

retrieved

30 October 2018

Congenital muscular dystrophy with 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=1114045

retrieved

10 December 2018

50th ENMC International Workshop: congenital muscular dystrophy. 28 February 1997 to 2 March 1997, Naarden, The Netherlands

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9765171

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

47th ENMC International Workshop: Treatment of Muscular Dystrophy. 13-15 December 1996, Naarden, The Netherlands

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9765171

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Muscular Dystrophy: Some Recent Advances in Knowledge

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9765171

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Proceedings of the First International Symposium on Oculopharyngeal muscular dystrophy. Québec, 22-23 September 1995

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9765171

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9765171

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myopathia distalis tarda hereditaria; 249 examined cases in 72 pedigrees

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9765171

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Amelioration of the dystrophic phenotype of mdx mice using a truncated utrophin transgene

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9765171

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Towards the classification of the autosomal recessive limb-girdle muscular dystrophies

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9765171

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetics of laminin α2 chain (or merosin) deficient congenital muscular dystrophy: from identification of mutations to prenatal diagnosis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9765171

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1136/BMJ.317.7164.991

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9765171

retrieved

29 July 2017

PMC publication ID

1114045

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9765171

retrieved

29 July 2017

PubMed publication ID

9765171

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9765171

retrieved

29 July 2017

 

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