The heart in limb girdle muscular dystrophy. (Q35366393)

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English	The heart in limb girdle muscular dystrophy.	scientific article

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instance of

scholarly article

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Europe PubMed Central

PMC publication ID

1728583

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9505924%20AND%20SRC:MED&resulttype=core&format=json

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10 November 2019

title

The heart in limb girdle muscular dystrophy (English)

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Europe PubMed Central

PMC publication ID

1728583

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9505924%20AND%20SRC:MED&resulttype=core&format=json

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10 November 2019

author name string

A J van der Kooi

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1

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Europe PubMed Central

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1728583

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9505924%20AND%20SRC:MED&resulttype=core&format=json

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10 November 2019

W G de Voogt

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2

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Europe PubMed Central

PMC publication ID

1728583

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9505924%20AND%20SRC:MED&resulttype=core&format=json

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10 November 2019

P G Barth

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3

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Europe PubMed Central

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1728583

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9505924%20AND%20SRC:MED&resulttype=core&format=json

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10 November 2019

H F Busch

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4

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1728583

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9505924%20AND%20SRC:MED&resulttype=core&format=json

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10 November 2019

F G Jennekens

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5

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Europe PubMed Central

PMC publication ID

1728583

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9505924%20AND%20SRC:MED&resulttype=core&format=json

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10 November 2019

P J Jongen

series ordinal

6

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Europe PubMed Central

PMC publication ID

1728583

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9505924%20AND%20SRC:MED&resulttype=core&format=json

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10 November 2019

M de Visser

series ordinal

7

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Europe PubMed Central

PMC publication ID

1728583

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9505924%20AND%20SRC:MED&resulttype=core&format=json

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10 November 2019

language of work or name

English

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publication date

1 January 1998

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PMC publication ID

1728583

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10 November 2019

published in

Heart

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stated in

Europe PubMed Central

PMC publication ID

1728583

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9505924%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

volume

79

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Europe PubMed Central

PMC publication ID

1728583

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9505924%20AND%20SRC:MED&resulttype=core&format=json

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10 November 2019

issue

1

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Europe PubMed Central

PMC publication ID

1728583

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9505924%20AND%20SRC:MED&resulttype=core&format=json

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10 November 2019

page(s)

73-77

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Europe PubMed Central

PMC publication ID

1728583

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9505924%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

cites work

Genetic localization of a newly recognized autosomal dominant limb-girdle muscular dystrophy with cardiac involvement (LGMD1B) to chromosome 1q11-21.

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=1728583

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27 July 2018

Chromosome 15-linked limb-girdle muscular dystrophy: clinical phenotypes in Reunion Island and French metropolitan communities

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=1728583

retrieved

27 July 2018

Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein

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=1728583

retrieved

27 July 2018

Linkage analysis in autosomal recessive limb-girdle muscular dystrophy (AR LGMD) maps a sixth form to 5q33-34 (LGMD2F) and indicates that there is at least one more subtype of AR LGMD

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=1728583

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27 July 2018

Juvenile limb-girdle muscular dystrophy. Clinical, histopathological and genetic data from a small community living in the Reunion Island

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=1728583

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27 July 2018

Dystrophin-associated proteins in 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=1728583

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27 July 2018

Limb girdle muscular dystrophy: a non-invasive cardiac evaluation

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=1728583

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27 July 2018

Missense mutations in the adhalin gene linked to autosomal recessive 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=1728583

retrieved

27 July 2018

A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2p

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=1728583

retrieved

27 July 2018

Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A

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=1728583

retrieved

27 July 2018

Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity

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=1728583

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27 July 2018

Beta-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex

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=1728583

retrieved

27 July 2018

Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 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=1728583

retrieved

27 July 2018

Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy: linkage of an autosomal dominant form to chromosome 5q

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=1728583

retrieved

27 July 2018

Confirmation of linkage of limb-girdle muscular dystrophy, type 2, to chromosome 15.

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=1728583

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27 July 2018

Subclinical cardiomyopathy in Becker 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=1728583

retrieved

27 July 2018

Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q.

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=1728583

retrieved

27 July 2018

Persistent Atrial Standstill with Limb Girdle 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=1728583

retrieved

27 July 2018

The clinical spectrum of limb girdle muscular dystrophy. A survey in The Netherlands

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=1728583

retrieved

26 September 2018

β–sarcoglycan: characterization and role in limb–girdle muscular dystrophy linked to 4q12

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=1728583

retrieved

26 September 2018

Clinical and genetic investigation in autosomal dominant limb-girdle 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=1728583

retrieved

15 November 2018

ECG differentiation of muscular dystrophy types

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9505924

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cardiomyopathy may be the only clinical manifestation in female carriers of Duchenne muscular dystrophy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9505924

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Cardiac involvement in certain muscular diseases. Apropos of 216 cases]

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9505924

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cardiomyopathy of limb-girdle muscular dystrophy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9505924

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Brief report: deficiency of a dystrophin-associated glycoprotein (adhalin) in a patient with muscular dystrophy and cardiomyopathy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9505924

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A newly recognized autosomal dominant limb girdle muscular dystrophy with cardiac involvement

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9505924

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormalities in alpha-, beta- and gamma-sarcoglycan in patients with limb-girdle muscular dystrophy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9505924

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The phenotype of chromosome 2p-linked limb-girdle muscular dystrophy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9505924

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Limb-girdle muscular dystrophy 2C: clinical aspects

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9505924

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The electrocardiogram in population studies. A classification system

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9505924

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The distinctive electrocardiogram of Duchenne's progressive muscular dystrophy. An electrocardiographic-pathologic correlative study

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9505924

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Cardiomyopathy in female carriers of the Duchenne gene]

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9505924

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant humeroperoneal myopathy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9505924

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Monoclonal antibodies against defined regions of the muscular dystrophy protein, dystrophin

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9505924

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A manifesting carrier of Duchenne muscular dystrophy with severe myocardial symptoms

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9505924

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A gene for limb-girdle muscular dystrophy maps to chromosome 15 by linkage

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9505924

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myocardial involvement in 2 women, carriers of Duchenne de Boulogne muscular dystrophy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9505924

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A symptomatic female patient with Duchenne muscular dystrophy diagnosed by dystrophin-staining: a case report

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9505924

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The heart in Becker muscular dystrophy, facioscapulohumeral dystrophy, and Bethlem myopathy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9505924

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

European Workshop on Emery-Dreifuss Muscular Dystrophy 1991

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9505924

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dystrophin negative skeletal and myocardial muscle cells in a carrier of Duchenne's muscular dystrophy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9505924

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1136/HRT.79.1.73

1 reference

stated in

Europe PubMed Central

PMC publication ID

1728583

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9505924%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

PMC publication ID

1728583

1 reference

stated in

Europe PubMed Central

PMC publication ID

1728583

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9505924%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

PubMed publication ID

9505924

1 reference

stated in

Europe PubMed Central

PMC publication ID

1728583

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9505924%20AND%20SRC:MED&resulttype=core&format=json

retrieved

10 November 2019

 

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