(Q24514959)

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Emery-Dreifuss syndrome

scientific article

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scholarly article

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1 reference

Europe PubMed Central

Emery-Dreifuss syndrome (English)

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author name string

A E Emery

1

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language of work or name

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publication date

October 1989

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Journal of Medical Genetics

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26

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10

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637-41

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New results of genetics of muscular dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015715

27 September 2017

Scapuloperoneal syndrome with cardiomyopathy: report of a family with autosomal dominant inheritance and unusual features

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015715

27 September 2017

X-linked scapuloperoneal syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015715

27 September 2017

The rigid spine syndrome--a myopathy of uncertain nosological position

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015715

27 September 2017

Familial lethal cardiomyopathy with mental retardation and scapuloperoneal muscular dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015715

27 September 2017

Emery-Dreifuss muscular dystrophy: report of five cases in a family and review of the literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015715

27 September 2017

X-linked muscular dystrophy with early contractures and cardiomyopathy (Emery-Dreifuss type).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015715

27 September 2017

Localisation of the gene for Emery-Dreifuss muscular dystrophy to the distal long arm of the X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015715

27 September 2017

Emery-Dreifuss muscular dystrophy: localisation to Xq27.3----qter confirmed by linkage to the factor VIII gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015715

27 September 2017

Adult onset scapuloperoneal myopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015715

27 September 2017

Immunostaining of skeletal and cardiac muscle surface membrane with antibody against Duchenne muscular dystrophy peptide

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015715

27 September 2017

Emery-Dreifuss syndrome and X-linked muscular dystrophy with contractures: evidence for homogeneity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015715

30 May 2018

X-linked pseudohypertrophic muscular dystrophy with a late onset and slow progression

1 reference

https://pubmed.ncbi.nlm.nih.gov/2685312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[A new x-chromosomal muscular dystrophy]

1 reference

https://pubmed.ncbi.nlm.nih.gov/2685312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Scapuloperoneal muscular atrophy with cardiopathy. An X-linked recessive trait

1 reference

https://pubmed.ncbi.nlm.nih.gov/2685312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Emery-dreifuss muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2685312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Atrioventricular block and supraventricular arrhythmias with X-linked muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2685312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Emery‐dreifuss humeroperoneal muscular dystorphy: An X‐linked myopathy with unusual contractures and bradycardia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2685312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Emery-Dreifuss muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2685312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genetic variant of Emery-Dreifuss disease. Muscular dystrophy with humeropelvic distribution, early joint contracture, and permanent atrial paralysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2685312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal-dominant dystrophy with humeroperoneal weakness and cardiopathy: a genetic variant of Emery-Dreifuss disease?

1 reference

https://pubmed.ncbi.nlm.nih.gov/2685312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Benign muscular dystrophy with contractures: a new syndrome?

1 reference

https://pubmed.ncbi.nlm.nih.gov/2685312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dominant autosomal muscular dystrophy with early contractures and cardiomyopathy (Hauptmann-Thannhauser)

1 reference

https://pubmed.ncbi.nlm.nih.gov/2685312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A linkage study of Emery-Dreifuss muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2685312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The rigid spine syndrome and Emery-Dreifuss muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2685312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two families of benign sex-linked recessive muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2685312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Emery-Dreifuss disease or syndrome of amyotrophy with early contractures and secondary disorders of cardiac conduction with variable heredity]

1 reference

https://pubmed.ncbi.nlm.nih.gov/2685312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Emery-Dreifuss muscular dystrophy. An autopsy case

1 reference

https://pubmed.ncbi.nlm.nih.gov/2685312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lethal cardiac conduction defects in Emery-Dreifuss muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2685312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of dystrophin in muscle-biopsy specimens from patients with Duchenne's or Becker's muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2685312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Emery-Dreifuss muscular dystrophy: disease spectrum and differential diagnosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2685312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping of the Emery-Dreifuss gene through reconstruction of crossover points in two Italian pedigrees

1 reference

https://pubmed.ncbi.nlm.nih.gov/2685312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant Emery-Dreifuss syndrome: evidence of a neurogenic variant of the disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/2685312

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.26.10.637

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