McArdle's disease presenting as recurrent cryptogenic renal failure due to occult seizures
Author:
Publisher
Wiley
Subject
Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology
Reference10 articles.
1. McArdle's disease: a nonsense mutation in exon 1 of the muscle glycogen phosphorylase gene explains some but not all cases
2. Clinical Spectrum of McArdle Disease: Three Cases with Unusual Expression
3. Glycogen storage diseases of muscle
4. Nonlysosomal glycogenoses. In: editors. Myology, 2nd ed. New York: McGraw-Hill; 1994. p 1554-1576.
Cited by 5 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. Rhabdomyolysis With Acute Renal Failure Requiring Dialysis in McArdle Disease;Journal of Clinical Psychopharmacology;2016-08
2. Recurrent Episodes of Rhabdomyolysis after Seizures in a Patient with Glycogen Storage Disease Type V;Journal of Clinical Neurology;2016
3. Pseudohypoglycemia Manifesting as Complex Partial Seizures in a Patient with Type III Glycogen Storage Disease;Puzzling Cases of Epilepsy;2008
4. Acute renal failure due to rhabdomyolysis in a child with McArdle disease;European Journal of Pediatrics;2007-09-26
5. McArdle disease with rhabdomyolysis induced by rosuvastatin: case report;Arquivos de Neuro-Psiquiatria;2007-09
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