Emery-Dreifuss muscular dystrophy - a 40 year retrospective (Q28145710)

Emery-Dreifuss muscular dystrophy

Europe PubMed Central

title

Emery-Dreifuss muscular dystrophy - a 40 year retrospective (English)

0 references

main subject

1 reference

A E Emery

1

0 references

language of work or name

English

0 references

publication date

June 2000

0 references

published in

Neuromuscular Disorders

0 references

volume

10

0 references

issue

4-5

0 references

page(s)

228-32

0 references

cites work

Unusual type of benign x-linked muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900105-X

7 January 2021

Emery-dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900105-X

7 January 2021

Cardiac involvement in Emery Dreifuss muscular dystrophy: a case series

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900105-X

7 January 2021

Emery-Dreifuss muscular dystrophy: disease spectrum and differential diagnosis

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900105-X

7 January 2021

Severe clinical expression in X-linked Emery–Dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900105-X

7 January 2021

60th ENMC International Workshop: non X-linked Emery-Dreifuss Muscular Dystrophy 5-7 June 1998, Naarden, The Netherlands

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900105-X

7 January 2021

Cardiac transplantation in female Emery-Dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900105-X

7 January 2021

Early presentation of X-linked Emery-Dreifuss muscular dystrophy resembling limb-girdle muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900105-X

7 January 2021

Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900105-X

7 January 2021

Emerin deficiency at the nuclear membrane in patients with Emery-Dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900105-X

7 January 2021

The Emery-Dreifuss muscular dystrophy protein, emerin, is a nuclear membrane protein

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900105-X

7 January 2021

Muscular dystrophies: alterations in a limited number of cellular pathways?

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900105-X

7 January 2021

Emerin deletions occurring on both Xq28 inversion backgrounds

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900105-X

7 January 2021

The Emery-Dreifuss Muscular Dystrophy Mutation Database

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900105-X

7 January 2021

Diagnosis of X-linked Emery-Dreifuss muscular dystrophy by protein analysis of leucocytes and skin with monoclonal antibodies

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900105-X

7 January 2021

Oral exfoliative cytology for the non-invasive diagnosis in X-linked Emery–Dreifuss muscular dystrophy patients and carriers

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900105-X

7 January 2021

Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900105-X

7 January 2021

cDNA sequencing of nuclear lamins A and C reveals primary and secondary structural homology to intermediate filament proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900105-X

7 January 2021

Mutational analysis using oligonucleotide microarrays

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900105-X

7 January 2021

Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900105-X

7 January 2021

Nuclear lamin A/C R482Q mutation in canadian kindreds with Dunnigan-type familial partial lipodystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900105-X

7 January 2021

Creatine kinase, cell membrane and Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900105-X

7 January 2021

Distinct regions specify the nuclear membrane targeting of emerin, the responsible protein for Emery-Dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900105-X

7 January 2021

Distribution of emerin during the cell cycle

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900105-X

7 January 2021

Nuclear proteins and cell death in inherited neuromuscular disease

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900105-X

7 January 2021

Heart-specific localization of emerin: new insights into Emery-Dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900105-X

7 January 2021

Distribution of emerin and lamins in the heart and implications for Emery-Dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900105-X

7 January 2021

Emerin and cardiomyopathy in Emery-Dreifuss muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900105-X

7 January 2021

Loss of A-type lamin expression compromises nuclear envelope integrity leading to muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2800%2900105-X

7 January 2021

10.1016/S0960-8966(00)00105-X

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

2738173

2738173

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference