Literature DB >> 14173855

SKELETAL MUSCLE GLYCOGENOSIS IN INDENTICAL TWINS.

T LEHOCZKY, M HALASY, G SIMON, G HARMOS.   

Abstract

Keywords:  BIOPSY; BLOOD CHEMICAL ANALYSIS; DIAGNOSIS; DISEASES IN TWINS; EXERCISE TEST; EXERTION; GLYCOGENOSIS; ISCHEMIA; MUCOPOLYSACCHARIDES; MUSCULAR DISEASES; PATHOLOGY; PYRUVATES

Mesh：

Substances：

Year:  1964        PMID： 14173855      PMCID： PMC1816520     

Source DB:  PubMed          Journal:  Br Med J        ISSN： 0007-1447


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  7 in total

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

Authors:  P A DI SANT'AGNESE; D H ANDERSEN; K M METCALF
Journal:  J Pediatr       Date:  1962-09       Impact factor: 4.406

2.  Glycogen metabolism.

Authors:  D STETTEN; M R STETTEN
Journal:  Physiol Rev       Date:  1960-07       Impact factor: 37.312

3.  Hereditary absence of muscle phosphorylase (McArdle's syndrome).

Authors:  R SCHMID; L HAMMAKER
Journal:  N Engl J Med       Date:  1961-02-02       Impact factor: 91.245

4.  A metabolic myopathy due to absence of muscle phosphorylase.

Authors:  C M PEARSON; D G RIMER; W F MOMMAERTS
Journal:  Am J Med       Date:  1961-04       Impact factor: 4.965

5.  [Neuromuscular form of glycogen storage disease].

Authors:  R SCHNABEL
Journal:  Virchows Arch Pathol Anat Physiol Klin Med       Date:  1958

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

Authors:  R SCHMID; R MAHLER
Journal:  J Clin Invest       Date:  1959-11       Impact factor: 14.808

7.  McArdle's syndrome: phosphorylase-deficient myopathy.

Authors:  R S MELLICK; R F MAHLER; B P HUGHES
Journal:  Lancet       Date:  1962-05-19       Impact factor: 79.321
  7 in total

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