(Q35490561)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14264721%20AND%20SRC:MED&resulttype=core&format=json

13 December 2019

review article

1 reference

title

THE CLINICAL BIOCHEMISTRY OF THE MUSCULAR DYSTROPHIES (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14264721%20AND%20SRC:MED&resulttype=core&format=json

13 December 2019

author name string

W H THOMSON

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14264721%20AND%20SRC:MED&resulttype=core&format=json

13 December 2019

publication date

1 January 1964

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14264721%20AND%20SRC:MED&resulttype=core&format=json

Advances in Clinical Chemistry

13 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14264721%20AND%20SRC:MED&resulttype=core&format=json

13 December 2019

volume

7

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14264721%20AND%20SRC:MED&resulttype=core&format=json

13 December 2019

page(s)

137-197

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14264721%20AND%20SRC:MED&resulttype=core&format=json

Studies on serum aldolase activity in neuromuscular disorders. I. Clinical applications

13 December 2019

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Serum aldolase activity in neuromuscular disorders. 2. Experimental application

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Concentrations of K and Na in skeletal muscle of mice with a hereditary myopathy (Dystrophia muscularis)

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The origin of urinary creatine in progressive muscular dystrophy

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Qualitative study of aminoaciduria in muscular dystrophy and myotonia dystrophica

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

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PSEUDOHYPERTROPHIC MUSCULAR DYSTROPHY. DISTRIBUTION OF DEGENERATIVE FEATURES AS REVEALED BY AN ANATOMICAL STUDY

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Glutamate-oxaloacetate transaminase isoenzymes in rat serum

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GENETICS AND DISEASES OF MUSCLE.

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A titrimetric method for the determination of creating phosphokinase

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Serum enzyme studies in muscular dystrophy. III. Serum malic dehydrogenase, 5-nucleotidase and adenosine-triphosphatase

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Urinary excretion of creatine in dermatomyositis

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Incorporation of glycine-I-C14 into nucleic acids and proteins of mice with hereditary muscular dystrophy

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[Serum creatine phosphokinase: determination and diagnostic significance]

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Serum glutamic oxalacetic transaminase in dermatomyositis

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Metabolism of myosin and life time of myofibrils

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[Study of arteriovenous differences during muscle diseases. 1. Oxygen, glucose & lactic acid. 2. Blood aldolase]

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7 January 2021

Biochemical study of muscle in progressive muscular dystrophy

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7 January 2021

On the function of the endocrine glands in myotonic muscular dystrophy

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7 January 2021

Progressive muscular dystrophy of the Duchenne type in females and its mode of inheritance.

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7 January 2021

MYOPATHIC CHANGES IN A MUSCULAR DYSTROPHY CARRIER

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7 January 2021

Electrophoretic Pattern of Lactic Dehydrogenase in Carriers and Patients with Duchenne Muscular Dystrophy

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7 January 2021

Serum aldolase and the diagnosis of myopathy.

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7 January 2021

Changes in serum enzyme levels after exercise in trained and untrained subjects

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7 January 2021

Dexamethasone myopathy

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7 January 2021

Lactic dehydrogenase activities of heart and skeletal muscle of exercised rats

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7 January 2021

Creatinephosphokinase levels in hypothyroidism

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7 January 2021

Alpha-tocohydroquinone and muscle dystrophy

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7 January 2021

Phosphoglucomutase Activity in Hereditary Muscular Dystrophy in Mice

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7 January 2021

Aldolase activity of the heart and skeletal muscle of exercised rats

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7 January 2021

[Enzyme activity determinations in healthy human musculature and in myopathies. II. Enzyme activity changes in muscle in progressive muscular dystrophy]

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7 January 2021

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

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7 January 2021

Serum Enzymes in Carriers of Muscular Dystrophy

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7 January 2021

Transaminase activity in human blood

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7 January 2021

Dependence of high serum aldolase on local circulation of injured muscle

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7 January 2021

Autosomal recessive inheritance of Duchennetype muscular dystrophy

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7 January 2021

Abnormalities of muscle protein metabolism in mice with muscular dystrophy

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7 January 2021

[Aldolase determinations in the serum in myotonic dystrophy]

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7 January 2021

17-Ketosteroids and their fractions in myotonic dystrophy

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7 January 2021

Creatine phosphokinase (CPK) of serum in myotonic dystrophy

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7 January 2021

Serum glutamic oxaloacetic transaminase activity in human acute transmural myocardial infarction

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An investigation of the carrier state in the Duchenne type muscular dystrophy

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7 January 2021

Myotonia congenita, dystrophia myotonica and paramyotonia; reaffirmation of their identity.

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7 January 2021

Dehydrogenase Activities in Dystrophic Mice

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7 January 2021

Muscle dystrophy in mice of the Bar Harbor strain; an electromyographic comparison with dystrophia myotonica in man

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7 January 2021

Reversible amyotrophy complicating treatment with fludrocortisone

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7 January 2021

Evaluation of glycolytic and citric acid cycles in homogenates of dystrophic mouse muscle

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7 January 2021

Dystrophia Muscularis: A HEREDITARY PRIMARY MYOPATHY IN THE HOUSE MOUSE.

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The myocardium--its biochemistry and biophysics. II. Biochemistry. The regulation of metabolism and energy release in contracting muscle

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7 January 2021

THE MUSCLE CELL AND ITS FUNCTIONAL ARCHITECTURE

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7 January 2021

Abnormal hepatic tests in muscular disease

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7 January 2021

Serum creatine phosphokinase. Activity in progressive muscular dystrophy and neuromuscular diseases

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7 January 2021

Progressive muscular dystrophy: The histopathological changes in skeletal muscle obtained by biopsy

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7 January 2021

A histological study of muscle from the Bar Harbor strain of dystrophic mice

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7 January 2021

Serum enzymes in muscular dystrophy and certain other muscular and neuromuscular diseases. I. Serum glutamic oxalacetic transaminase

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7 January 2021

Rheumatic manifestations of polymyositis and dermatomyositis

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7 January 2021

Histopathological features of muscle in the preclinical stages of muscular dystrophy

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7 January 2021

MUSCULAR DYSTROPHY. REVIEW AND RECENT OBSERVATIONS.

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7 January 2021

X-chromosome mosaicism in females with muscular dystrophy

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7 January 2021

The problem of anticipation in pedigrees of dystrophia myotonica

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7 January 2021

THE CHEMICAL COMPOSITION OF VOLUNTARY MUSCLE IN MUSCLE DISEASE: A COMPARISON OF PROGRESSIVE MUSCULAR DYSTROPHY WITH OTHER DISEASES TOGETHER WITH A STUDY OF EFFECTS OF GLYCINE AND CREATINE THERAPY.

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7 January 2021

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

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7 January 2021

[Changes in aldolase activity in the blood serum during muscular work]

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7 January 2021

[Progressive muscular dystrophy. I. The heterogenicity of serum lactic dehydrgenase]

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7 January 2021

Distribution of high energy phosphate in normal and dystrophic muscle

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7 January 2021

Ribosuria in Muscular Dystrophy

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7 January 2021

Multiple Serial Enzyme Studies in Acute Myocardial Infarction

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7 January 2021

Serum aldolase in muscular dystrophies, neuromuscular disorders, and wasting of skeletal muscle

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7 January 2021

The effect of physical exercise on serum transaminase

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7 January 2021

Plasma enzyme activity in myocardial infarction in dog and man

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7 January 2021

Turnover of muscle and liver proteins in mice with hereditary muscular dystrophy

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7 January 2021

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

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7 January 2021

Activity of serum aldolase and lactic dehydrogenase in patients affected with Duchenne muscular dystrophy and in their immediate relatives

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7 January 2021

Evidence on inheritance of muscular dystrophy in an inbred strain of mice using ovarian transplantation

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7 January 2021

Increased lysosomal enzymes in genetic muscular dystrophy

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7 January 2021

Serum aldolase in muscle disease

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7 January 2021

Tonische Krämpfe in willkürlich beweglichen Muskeln in Folge von ererbter psychischer Disposition

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7 January 2021

Sources of error in the biochemical diagnosis of muscular dystrophy

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7 January 2021

A trial of therapy by nucleosides and nucleotides in muscular dystrophy

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7 January 2021

Serum enzyme activity in muscular dystrophy.

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7 January 2021

Skeletal muscle glycogenosis: an investigation of two dissimilar cases

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7 January 2021

A biochemical study of certain skeletal muscle constituents in human progressive muscular dystrophy

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7 January 2021

Evidence of regeneration in repeat biopsies of dystrophic human muscle

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7 January 2021

Ribosuria in muscular dystrophy

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7 January 2021

On the classification, natural history and treatment of the myopathies.

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7 January 2021

Enzyme studies in muscular dystrophy. III. In hereditary muscular dystrophy in mice

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Histopathology of hereditary, progressive muscular dystrophy in inbred strain 129 mice

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7 January 2021

Some alterations in serum enzymes in progressive muscular dystrophy

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7 January 2021

Electrolyte levels in normal and dystrophic muscle determined by neutron activation

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7 January 2021

Triamcinolone myopathy

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7 January 2021

Lactic dehydrogenase activity in blood

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7 January 2021

Serum glutamic pyruvic transaminase in cardiac with hepatic disease

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7 January 2021

The mechanisms of alteration in lactic dehydrogenase activity of body fluids

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7 January 2021

Movement of aldolase from excised rat diaphragm

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7 January 2021

Effect of potassium-rich medium, of glucose and of transfer of tissue on oxygen consumption by rat diaphragm

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7 January 2021

Diffusion of aldolase from rat skeletal muscle; an index of membrane permeability

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7 January 2021

Increased muscle permeability to aldolase produced by depolarization and by metabolic inhibitors

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7 January 2021

Muscle membrane as a dynamic structure and its permeability to aldolase

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Identifiers

DOI

1 reference

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13 December 2019

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