酸性麦芽糖酶缺乏症的谱系及诊断 - Suppr

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The spectrum and diagnosis of acid maltase deficiency.

作者信息

Engel A G, Gomez M R, Seybold M E, Lambert E H

出版信息

Neurology. 1973 Jan;23(1):95-106. doi: 10.1212/wnl.23.1.95.

DOI:10.1212/wnl.23.1.95

PMID:4510595

Abstract

摘要

相似文献

The spectrum and diagnosis of acid maltase deficiency.酸性麦芽糖酶缺乏症的谱系及诊断

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Type 3 glycogenosis. An adult with diffuse weakness and muscle wasting.

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Reduced muscle alpha-glucosidase (acid-maltase) activity in hypothyroid myopathy.甲状腺功能减退性肌病中肌肉α-葡萄糖苷酶（酸性麦芽糖酶）活性降低。

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Adult myopathy from glycogen storage disease due to acid maltase deficiency.由于酸性麦芽糖酶缺乏导致糖原贮积病引起的成人肌病。

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Late infantile acid maltase deficiency.晚发性婴儿酸性麦芽糖酶缺乏症

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Fingerprint body myopathy, a newly recognized congenital muscle disease.指纹体肌病，一种新发现的先天性肌肉疾病。

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[Histological, serum enzyme and electromyographic studies in thyreomyopathies in children (research on hypothroid patients)].[儿童甲状腺肌病的组织学、血清酶及肌电图研究（对甲状腺功能减退患者的研究）]

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[McArdle's metabolic myopathy].[麦卡德尔代谢性肌病]

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