Unusual type of benign x-linked muscular dystrophy (Q24519418)

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English	Unusual type of benign x-linked muscular dystrophy	scientific article

Statements

instance of

scholarly article

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stated in

Europe PubMed Central

PubMed publication ID

5969090

retrieved

21 June 2017

title

Unusual type of benign x-linked muscular dystrophy (English)

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Europe PubMed Central

PubMed publication ID

5969090

retrieved

21 June 2017

main subject

muscular dystrophy

1 reference

based on heuristic

inferred from title

surgery

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stated in

Crossref

DOI

10.1136/JNNP.29.4.338

reference URL

https://api.crossref.org/works/10.1136/JNNP.29.4.338

retrieved

17 July 2023

author name string

A. E. Emery

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5969090

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5969090

retrieved

17 July 2023

F. E. Dreifuss

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5969090

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5969090

retrieved

17 July 2023

language of work or name

English

0 references

publication date

1 August 1966

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Europe PubMed Central

PubMed publication ID

5969090

retrieved

21 June 2017

full work available at URL

https://europepmc.org/articles/PMC1064196

file format

HTML

online access status

open access

content deliverer

Europe PubMed Central

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5969090

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5969090

retrieved

17 July 2023

https://europepmc.org/articles/PMC1064196?pdf=render

file format

Portable Document Format

online access status

open access

content deliverer

Europe PubMed Central

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5969090

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5969090

retrieved

17 July 2023

https://syndication.highwire.org/content/doi/10.1136/jnnp.29.4.338

1 reference

stated in

Crossref

DOI

10.1136/JNNP.29.4.338

reference URL

https://api.crossref.org/works/10.1136/JNNP.29.4.338

retrieved

17 July 2023

published in

Journal of Neurology, Neurosurgery and Psychiatry

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5969090

retrieved

21 June 2017

volume

29

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stated in

Europe PubMed Central

PubMed publication ID

5969090

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21 June 2017

issue

4

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stated in

Europe PubMed Central

PubMed publication ID

5969090

retrieved

21 June 2017

page(s)

338-342

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Europe PubMed Central

PubMed publication ID

5969090

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21 June 2017

cites work

New results of genetics of 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=1064196

retrieved

27 September 2017

Muscular dystrophy in childhood; the genetic aspect; a field study in the Leeds region of clinical types and their inheritance.

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=1064196

retrieved

29 November 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=1064196

retrieved

29 November 2018

Progressive muscular dystrophy. VII. Detection of heterozygotes of Duehenne muscular dystrophy by determining serum creatine kinase with localized work load in anoxia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5969090

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

THE HEART IN PROGRESSIVE MUSCULAR DYSTROPHY

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5969090

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cardiac involvement in progressive muscular dystrophy

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5969090

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Survival in x-chromosomal muscular dystrophy

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5969090

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5969090

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical, genetic and electrocardiographic studies in childhood muscular dystrophy

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5969090

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cardiac and pulmonary complications in Duchenne's progressive muscular dystrophy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5969090

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The heart in progressive muscular dystrophy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5969090

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Creatine and creatine kinase measurement

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5969090

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intellectual function in childhood progressive muscular dystrophy

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5969090

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[A new x-chromosomal muscular dystrophy]

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5969090

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

On the inheritance of muscular dystrophy; with a note on the blood groups, and a note on colour vision and linkage studies

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5969090

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary myopathies

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5969090

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mental retardation in association with progressive dystrophy

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5969090

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myocardial disease associated with progressive muscular dystrophy; a report of 2 cases

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5969090

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

THE EFFECTS OF PREGNANCY ON THE CONCENTRATION OF CREATINE KINASE IN SERUM, SKELETAL MUSCLE, AND MYOMETRIUM

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5969090

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CARDIAC FINDINGS IN 73 PATIENTS WITH MUSCULAR DYSTROPHY

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5969090

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The heart in progressive muscular dystrophy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5969090

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CREATINE KINASE LEVELS IN WOMEN WHO CARRY GENES FOR THREE TYPES OF MUSCULAR DYSTROPHY

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/5969090

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intellectual Impairment in Muscular Dystrophy

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1136%2FJNNP.29.4.338

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

SERUM ENZYME STUDIES IN MUSCLE DISEASE. I. VARIATIONS IN SERUM CREATINE KINASE ACTIVITY IN NORMAL INDIVIDUALS.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1136%2FJNNP.29.4.338

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

DOI

10.1136/JNNP.29.4.338

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5969090

retrieved

21 June 2017

PMC publication ID

1064196

0 references

PubMed publication ID

5969090

1 reference

stated in

Europe PubMed Central

PubMed publication ID

5969090

retrieved

21 June 2017

ResearchGate publication ID

17217307

0 references

 

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