Familial myoadenylate deaminase deficiency and exertional myalgia
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Neurology (clinical)
Cited by 71 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Skeletal muscle contraction kinetics and AMPK responses are modulated by the adenine nucleotide degrading enzyme AMPD1;Journal of Applied Physiology;2022-11-01
2. Rhabdomyolysis and Myoglobinuria;Neuromuscular Disorders in Clinical Practice;2013-04-26
3. Primary Adenosine Monophosphate (AMP) Deaminase Deficiency in a Hypotonic Infant;Journal of Child Neurology;2011-02-22
4. Muscle Histopathology and Physiology in Chronic Fatigue Syndrome;Ciba Foundation Symposium 173 - Chronic Fatigue Syndrome;2007-09-28
5. The impact of the AMPD1 gene polymorphism on exercise capacity, other prognostic parameters, and survival in patients with stable congestive heart failure: A study in 686 consecutive patients;American Heart Journal;2006-10
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