144th ENMC International Workshop: Outcome Measures in McArdle Disease, 29 September–1 November 2006, Naarden, The Netherlands
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
Reference24 articles.
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2. Chronic progressive myopathy with myoglobinuria: demonstration of a glycogenolytic defect in muscle;Schmidt;J Clin Invest,1959
3. Spontaneous “second wind” and glucose-induced second “second wind” in McArdle disease – oxidative mechanisms;Haller;Arch Neurol,2002
4. Do carriers of PYGM mutations have symptoms of McArdle disease?;Andersen;Neurology,2006
5. McArdle’s disease a nonsense mutation in exon 1 of the muscle glycogen phosphorylase gene explains some but not all cases;Bartram;Hum Mol Genet,1993
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1. Misdiagnosis is an important factor for diagnostic delay in McArdle disease;Neuromuscular Disorders;2017-09
2. Heart rate and perceived muscle pain responses to a functional walking test in McArdle disease;Journal of Sports Sciences;2014-04-14
3. Disorders of Muscle Glycogen Metabolism;Muscle Disease;2013-07-08
4. Physical training for McArdle disease;Cochrane Database of Systematic Reviews;2011-12-07
5. Physical training for McArdle disease;Cochrane Database of Systematic Reviews;2009-07-08
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