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patient deficiency muscle haemolytic anaemia phosphoglycerate kinase pgk deficiency haemolytic anaemia exercise activity glycogenosi disease myoglobinuria brother phosphoglycerate kinase university hospital mcardle stiffness muscle phosphofructokinase deficiency glycogenosis type vii phosphoglycerate kinase deficiency glycogenosis type v retardation tarui defect phosphofructokinase cramp university lactate episode blood right arm control symptom fibroblast phosphoglycerate mutase erythrocyte hospital dimauro family glycogenosis vii glycogenosis v acid metabolism glycolytic exercise intolerance cause myophosphorylase deficiency increase muscle nerve neurology rhabdomyolysi school trondheim exercise-induced stiffness krietsch ischaemic necrosis nerve conduction velocities bnmol /min protein dr jan aasly tsujino nmol /min protein glycogen protein tissue phosphorylase subjects patient 1 value presentation muscle phosphorylase activity manifestation exercise-induced myophosphorylase times maintenance fluids motor unit potentials eur j clin table familial-reduced pgk activity nerve
1 Most Recent Publications
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Phosphoglycerate kinase deficiency in two brothers with McArdle-like clinical symptoms
(Article)
Aasly, J. Diggelen, O.P. van Boer, A.M. Bronstad, G. |
2000-12-01
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