(Q36769943)

16 August 2017

McArdle's syndrome: a review and a preliminary report of four further cases (English)

1 reference

16 August 2017

R. H. Salter

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6042392

26 July 2023

language of work or name

English

0 references

publication date

1 May 1967

1 reference

PMC publication ID

2466173

full work available at URL

16 August 2017

https://europepmc.org/articles/PMC2466173

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6042392

https://europepmc.org/articles/PMC2466173?pdf=render

26 July 2023

file format

Portable Document Format

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6042392

https://academic.oup.com/pmj/article-pdf/43/499/365/50387601/postgradmedj-43-365.pdf

26 July 2023

file format

Portable Document Format

1 reference

Crossref

https://api.crossref.org/works/10.1136/PGMJ.43.499.365

Postgraduate Medical Journal

26 July 2023

published in

1 reference

16 August 2017

43

1 reference

16 August 2017

499

1 reference

16 August 2017

365-371

1 reference

A FUNCTIONAL DISORDER OF MUSCLE ASSOCIATED WITH THE ABSENCE OF PHOSPHORYLASE.

16 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2466173

Chronic progressive myopathy with myoglobinuria: demonstration of a glycogenolytic defect in the muscle

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2466173

A CASE OF MCARDLE'S SYNDROME WITH A POSITIVE FAMILY HISTORY.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2466173

A metabolic myopathy due to absence of muscle phosphorylase

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2466173

MCARDLE'S DISEASE PRESENTING AS CONVULSION AND RHABDOMYOLYSIS

29 September 2017

1 reference

12 December 2020

Contracture in McArdle's disease. Stability of adenosine triphosphate during contracture in phosphorylase-deficient human muscle

1 reference

12 December 2020

A FAMILY STUDY OF PHOSPHORYLASE DEFICIENCY IN MUSCLE.

1 reference

12 December 2020

MCARDLE'S DISEASE. HEREDITARY MYOPATHY DUE TO ABSENCE OF MUSCLE PHOSPHORYLASE

1 reference

12 December 2020

MCARDLE'S SYNDROME WITH PREVIOUSLY UNREPORTED ELECTROCARDIOGRAPHIC AND SERUM ENZYME ABNORMALITIES

1 reference

12 December 2020

McArdle's syndrome: phosphorylase-deficient myopathy

1 reference

12 December 2020

Hereditary absence of muscle phosphorylase (McArdle's syndrome)

1 reference

12 December 2020

Myopathy due to a defect in muscle glycogen breakdown

series ordinal

5

1 reference

Crossref

https://api.crossref.org/works/10.1136/PGMJ.43.499.365

Histopathology of Voluntary Muscle

26 July 2023

series ordinal

9

1 reference

Crossref

https://api.crossref.org/works/10.1136/PGMJ.43.499.365

26 July 2023

Identifiers

1 reference

16 August 2017

1 reference

PMC publication ID

2466173

16 August 2017

1 reference

PMC publication ID

2466173