Unique Exercise Lactate Profile in Muscle Phosphofructokinase Deficiency (Tarui Disease); Difference Compared with McArdle Disease

Author:

Piirilä Päivi,Similä Minna E.,Palmio Johanna,Wuorimaa Tomi,Ylikallio Emil,Sandell Satu,Haapalahti Petri,Uotila Lasse,Tyynismaa Henna,Udd Bjarne,Auranen Mari

Publisher

Frontiers Media SA

Subject

Clinical Neurology,Neurology

Reference28 articles.

1. Common mutations in the phosphofructokinase-M gene in Ashkenazi Jewish patients with glycogenesis VII – and their population frequency;Sherman;Am J Hum Genet,1994

2. Functional expression of human mutant phosphofructokinase in yeast: genetic defects in French Canadian and Swiss patients with phosphofructokinase deficiency;Raben;Am J Hum Genet,1995

3. Erythrocyte glucolysis and its marked alteration by muscular exercise in type VII glycogenosis;Shimizu;Blood,1998

4. Respiratory gas exchange and metabolic responses during exercise in McArdle’s disease;Riley;J Appl Physiol,1993

5. Metabolic myopathies: functional evaluation by different exercise testing approaches;Volpi;Musculoskelet Surg,2011

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