McArdle's Disease

Author:

Martinuzzi Andrea,Schievano Giuliana,Nascimbeni Annachiara,Fanin Marina

Publisher

Elsevier BV

Subject

Pathology and Forensic Medicine

Reference22 articles.

1. Nonlysosomal glycogenoses;Di Mauro,1994

2. Human brain glycogen phosphorylase: cloning, sequence analysis, chromosomal mapping, tissue expression and comparison with the human liver and muscle isozymes;Newgard;J Biol Chem,1988

3. Developmental expression of glycogenolytic enzymes in rabbit tissues: possible relationship to fetal lung maturation;Newgard;Biochim Biophys Acta,1991

4. The molecular genetic basis of myophosphorylase deficiency (McArdle's disease);Tsujino;Muscle Nerve,1995

5. Mutation analysis in myophosphorylase deficiency (McArdle's disease);Vorgerd;Ann Neurol,1998

Cited by 16 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. Results of an open label feasibility study of sodium valproate in people with McArdle disease;Neuromuscular Disorders;2020-09

2. Glycogenosis Type 5, McArdle Disease;Genetic Neuromuscular Disorders;2017-10-06

3. Differential Muscle Involvement in Mice and Humans Affected by McArdle Disease;Journal of Neuropathology & Experimental Neurology;2016-03-30

4. Metabolic Myopathies;Seminars in Neurology;2015-10-06

5. Minimal symptoms in McArdle disease: A real PYGM genotype effect?;Muscle & Nerve;2015-09-24

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