(Q39241159)

10 September 2017

Neurogenic scapuloperoneal syndrome in childhood (English)

1 reference

10 September 2017

Mercelis R

1

1 reference

10 September 2017

Demeester J

series ordinal

2

1 reference

10 September 2017

Martin JJ

series ordinal

3

1 reference

10 September 2017

language of work or name

English

0 references

publication date

1 October 1980

1 reference

Journal of Neurology, Neurosurgery and Psychiatry

10 September 2017

1 reference

10 September 2017

43

1 reference

10 September 2017

10

1 reference

10 September 2017

888-896

1 reference

Unusual type of benign x-linked muscular dystrophy

10 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=490709

Data on the distribution of fibre types in thirty-six human muscles. An autopsy study

10 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=490709

X-linked scapuloperoneal syndrome

10 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=490709

Adult onset scapuloperoneal myopathy

10 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=490709

Cardiac Features of an Unusual X-Linked Humeroperoneal Neuromuscular Disease

10 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=490709

Congenital fibre type disproportion myopathy. A histological diagnosis with an uncertain clinical outlook

10 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=490709

Scapuloperoneal atrophy with sensory involvement: Davidenkow's syndrome

10 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=490709

The differential diagnosis of scapuloperoneal amyotrophy

10 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=490709

Scapuloperoneal atrophy from myogen origin

10 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=490709

A neuromuscular syndrome of scapuloperoneal distribution.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=490709

A case of scapulo-tibio-peroneal syndrome. Electromyographic and histoenzymologic considerations.

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=490709

Histochemical and quantitative analysis of muscle biopsies.

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=490709

Scapulo-peroneal muscular atrophy. Full autopsy report. Unusual findings in the anterior horn of the spinal cord. Lipid storage in muscle

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=490709

Scapuloperoneal muscular atrophy

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=490709

The Neurogenic Scapulo-Peroneal Syndrome

21 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=490709

Spinal muscular atrophy of the scapulo-peroneal-type

21 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=490709

The differential diagnosis of the myogenic (facio)-scapulo-peroneal syndrome

21 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=490709

[A new kinship with X-chromosomal benign progressive muscular dystrophy and early contractures (Emery-Dreifuss)]

4 November 2018

1 reference

12 December 2020

Scapuloperoneal dystrophy associated with neurogenic changes

1 reference

12 December 2020

Quantitative histological and neurophysiological studies in scapulo-peroneal syndrome

1 reference

12 December 2020

Scapulo-peroneal myopathies 14 cases including 8 with facial involvement

1 reference

12 December 2020

A Spinal Muscular Atrophy With Scapuloperoneal Distribution

1 reference

12 December 2020

Scapuloperoneal dystrophy and scapuloperoneal atrophy

1 reference

12 December 2020

Infantile scapuloperoneal muscular atrophy

1 reference

12 December 2020

New type of recessive X-linked muscular dystrophy: scapulo-humeral-distal muscular dystrophy with early contractures and cardiac arrhythmias

1 reference

12 December 2020

[Stark-Kaeser type of chronic scapulo-peroneal amyotrophy. Apropos of 10 cases]

1 reference

12 December 2020

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

1 reference

12 December 2020

[On the nosological role of the scapulo-peroneal syndrome]

1 reference

12 December 2020

Scapuloperoneal Amytrophy

1 reference

12 December 2020

Is congenital fibre type disproportion a true myopathy?

1 reference

12 December 2020

[Nosological position of so-called scapulo-peroneal syndrome]

1 reference

12 December 2020

The sciatic nerve in juvenile metachromatic leucodystrophy: a quantitative evaluation

1 reference

12 December 2020

[Clinical and genetic study of a family with progressive neuropathic muscular atrophy (Charcot-Marie amyotrophy).]

1 reference

12 December 2020

Myogenic scapuloperoneal syndrome - muscular dystrophy in the K. kindred. Reexamination of the K. family described for the first time by Oransky in 1927

1 reference

12 December 2020

Emery-dreifuss muscular dystrophy

1 reference

12 December 2020

Identifiers

DOI

10.1136/JNNP.43.10.888

1 reference

10 September 2017

1 reference

10 September 2017

PubMed publication ID

7441268

1 reference