(Q55405135)

7 July 2018

title

Detection of carriers of benign X-linked muscular dystrophy (English)

1 reference

Crossref

DOI

https://api.crossref.org/works/10.1136/BMJ.4.5578.522

29 July 2023

1 reference

https://api.crossref.org/works/10.1136/BMJ.4.5578.522

29 July 2023

author name string

A. E. Emery

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:6065987

29 July 2023

E. R. Clack

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:6065987

29 July 2023

S. Simon

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:6065987

29 July 2023

J. L. Taylor

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:6065987

29 July 2023

language of work or name

English

0 references

publication date

1 December 1967

1 reference

7 July 2018

full work available at URL

https://europepmc.org/articles/PMC1749119

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:6065987

https://europepmc.org/articles/PMC1749119?pdf=render

29 July 2023

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:6065987

https://syndication.highwire.org/content/doi/10.1136/bmj.4.5578.522

29 July 2023

1 reference

Crossref

DOI

https://api.crossref.org/works/10.1136/BMJ.4.5578.522

29 July 2023

1 reference

7 July 2018

volume

4

1 reference

7 July 2018

issue

5578

1 reference

7 July 2018

page(s)

522-523

1 reference

7 July 2018

Unusual type of benign x-linked muscular dystrophy

cites work

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1749119

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

9 July 2018

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1749119

A method for the estimation of serum creatine kinase and its use in comparing creatine kinase and aldolase activity in normal and pathological sera

12 August 2018

1 reference

12 December 2020

[Genetics of myopathy]

1 reference

12 December 2020

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

1 reference

12 December 2020

ACTIVATION OF CREATINE PHOSPHOKINASE BY SULFHYDRYL COMPOUNDS IN NORMAL AND MUSCULAR DYSTROPHY SERA

1 reference

12 December 2020

Creatine and creatine kinase measurement

1 reference

12 December 2020

A benign X-chromosomal hereditary muscular dystrophy. I. Examinations of symptom-carriers

1 reference

12 December 2020

Hereditary myopathies

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

1 reference

7 July 2018

PMC publication ID

1749119

1 reference

7 July 2018

1 reference

7 July 2018