Impairment of the exercise-induced increase in muscle perfusion in McArdle's disease

Author:

Jehenson Philippe,Leroy-Willig Anne,de Kerviler Eric,Merlet Pascal,Duboc Denis,Syrota André

Publisher

Springer Science and Business Media LLC

Subject

Radiology Nuclear Medicine and imaging,General Medicine,Radiology Nuclear Medicine and imaging,General Medicine

Reference24 articles.

1. McArdle B. Myopathy due to a defect in muscle glycogen breakdown.Clin Sci 1951; 10: 13?35.

2. Tsujino S, Shanske S, Di Mauro S. Molecular genetics heterogeneity of myophosphorylase deficiency (McArdle's disease).N Engl JMed 1993; 329: 241?245.

3. Porte D, Crawford DW, Jennings DB, Aber C, McIlroy MB. Cardiovascular and metabolic responses to exercise in a patient with McArdle's syndrome.N Engl J Med 1966; 275: 406?412.

4. Barcroft H, Greenwood B, McArdle B, et al. The effect of exercise on forearm blood perfusion and on venous blood pH, pCO2 and lactate in a subject with phosphorylase deficiency in skeletal muscle (McArdle's syndrome) [abstract]J Physiol (Lond) 166; 189: 44P?46P.

5. Lewis SF, Haller RG, Cook JD, Bloomqvist CG. Metabolic control of cardiac output response to exercise in McArdle's disease. J Appl Physiol 1984; 57: 1749?1753.

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