Metabolic Myopathies
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Genetics (clinical),Neurology (clinical)
Reference90 articles.
1. Gender differences in leucine kinetics and nitrogen balance in endurance athletes
2. Myoadenylate Deaminase Deficiency: A New Disease of Muscle
3. Exertional Rhabdomyolysis
4. A G468-T AMPD1 mutant allele contributes to the high incidence of myoadenylate deaminase deficiency in the Caucasian population
5. The effect of AMPD1 genotype on blood flow response to sprint exercise
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1. Metabolic Myopathies in the Era of Next-Generation Sequencing;Genes;2023-04-22
2. Lactate and ammonia measurements during cardiopulmonary exercise testing and its recovery phase—Consideration of age and sex in its interpretation;Clinical Physiology and Functional Imaging;2023-03-29
3. From recurrent rhabdomyolysis in a young adult to carnitine palmitoyltransferase II deficiency;Archive of Clinical Cases;2023-03-14
4. Pathophysiology and Management of Fatigue in Neuromuscular Diseases;International Journal of Molecular Sciences;2023-03-05
5. CONVENTIONAL APPROACHES TO THE THERAPY OF HEREDITARY MYOPATHIES;Pharmacy & Pharmacology;2022-12-11
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