Skeletal muscle glycogenosis: an investigation of two dissimilar cases (Q39414224)

11 September 2017

Skeletal muscle glycogenosis: an investigation of two dissimilar cases (English)

1 reference

11 September 2017

THOMSON WH

1

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11 September 2017

MACLAURIN JC

series ordinal

2

1 reference

11 September 2017

PRINEAS JW

series ordinal

3

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11 September 2017

language of work or name

English

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publication date

1 February 1963

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Journal of Neurology, Neurosurgery and Psychiatry

11 September 2017

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11 September 2017

26

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11 September 2017

60-68

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

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=495536

Sources of error in the biochemical diagnosis of muscular dystrophy

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=495536

A metabolic myopathy due to absence of muscle phosphorylase

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=495536

Familial cirrhosis of the liver with storage of abnormal glycogen

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=495536

A titrimetric method for the determination of creating phosphokinase

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=495536

Spectrophotometric determination of fructose-1:6-diphosphate, hexosemonophosphates, adenosinetriphosphate and adenosinediphosphate

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=495536

Serum enzyme activity in muscular dystrophy.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=495536

Progressive muscular dystrophy. II. Biochemical identification of the carrier state in the recessive sex-linked juvennile (Duchenne) type by serum creatine-phosphokinase determinations

21 August 2018

1 reference

12 December 2020

Glycogen storage disease of the muscles. Report of a case with unusual features

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12 December 2020

Amylo-1, 6-glucosidase in muscle tissue in generalized glycogen storage disease

1 reference

12 December 2020

A uridine coenzyme-linked pathway of glycogen synthesis in muscle

1 reference

12 December 2020

1 reference

12 December 2020

The relationship of epinephrine and glucagon to liver phosphorylase. I. Liver phosphorylase; preparation and properties

1 reference

12 December 2020

Diseases of glycogen storage with special reference to the cardiac type of generalized glycogenosis

1 reference

12 December 2020

McArdle's syndrome: phosphorylase-deficient myopathy

1 reference

12 December 2020

A colorimetric method for the determination of serum glutamic oxalacetic and glutamic pyruvic transaminases

1 reference

12 December 2020

Hereditary absence of muscle phosphorylase (McArdle's syndrome)

1 reference

12 December 2020

The molecular structure of glycogens

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12 December 2020

Evidence for direct utilization of fructose in working muscle in man

1 reference

12 December 2020

Identifiers

DOI

10.1136/JNNP.26.1.60

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11 September 2017

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11 September 2017

PubMed publication ID

13981250

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