A non-ischemic forearm exercise test for the screening of patients with exercise intolerance

Neurology

Volumn 56, Issue 12, 2001, Pages 1733-1738

  Hogrel, Jean Yves ^a   Laforet P ^a   Ben Yaou, R ^a   Chevrot, M ^a   Eymard, B ^a   Lombes A ^a  

^a PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

AMMONIA; CREATINE KINASE; GLYCOGEN; GLYCOGEN PHOSPHORYLASE; LACTIC ACID;

ADULT; CLINICAL ARTICLE; CONTROLLED STUDY; EXERCISE TEST; FEMALE; FOREARM; FUNCTIONAL ASSESSMENT; GLYCOGEN STORAGE DISEASE; HUMAN; LACTATE BLOOD LEVEL; MALE; MYOPATHY; PRIORITY JOURNAL; REVIEW; RHABDOMYOLYSIS; SAFETY; SCREENING TEST; STANDARDIZATION;

EID: 0035954322     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.56.12.1733     Document Type: Review

References (18)

1. Myopathy due to a defect in muscle glycogen breakdown
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3. Ischemic exercise test: Failure to detect partial expression of McArdle's disease
4. A standardized forearm ischemic exercise test
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6. Sympathetic activation in exercise is not dependent on muscle acidosis: Direct evidence from studies in metabolic myopathies
7. The forearm ischaemic work test: Hazardous to McArdle patients?
8. Early onset myophosphorylase deficiency (McArdle's disease) with absence of myophosphorylase protein on SDS electrophoresis: The role of the ischemic forearm test
9. Metabolic myopathies
10. No need for ischemia in the forearm exercise test for McArdle's disease
11. The relation between blood lactate and ammonia in ischemic handgrip exercise
12. Improvement of screening in exertional myalgia with a standardized ischemic forearm test
13. Medical implications of the lactate and ammonia relationship in anaerobic exercise
14. Behaviour of human motor units in different muscles during linearly varying contractions
15. Lactate in fast and slow twitch skeletal muscle fibres of man during isometric contraction
16. Forearm semi-ischemic exercise test in pediatric patients
17. Excess purine degradation in exercising muscles of patients with glycogen storage disease type V et VII
18. Mitochondrial myopathies