Histopathology of McArdle's disease in a family.
作者信息
Bale P, Hammett J F, Neale F C
出版信息
J Pathol Bacteriol. 1967 Oct;94(2):293-300. doi: 10.1002/path.1700940206.
PMID:6066477
Abstract
摘要
相似文献
1
Histopathology of McArdle's disease in a family.一个家族中麦卡德尔病的组织病理学
J Pathol Bacteriol. 1967 Oct;94(2):293-300. doi: 10.1002/path.1700940206.
2
[Apropos of a further case of absence of phosphorylase in the striated muscle (McArdle's disease)].[关于一例横纹肌中磷酸化酶缺乏的进一步病例（麦克尔迪氏病）]
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McArdle's syndrome (myophosphorylase deficiency). A study of a family.麦卡德尔综合征（肌磷酸化酶缺乏症）。一个家族的研究。
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[McArdle's metabolic myopathy].[麦卡德尔代谢性肌病]
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Acute renal failure in McArdle's disease. Report of two cases.麦克尔（McArdle）病中的急性肾衰竭。两例报告。
N Engl J Med. 1972 Jun 8;286(23):1237-41. doi: 10.1056/NEJM197206082862304.
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[McArdle's disease].[麦克尔憩室病]
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7
Myopathy resembling McArdle's syndrome.
Arch Neurol. 1969 Jun;20(6):586-98. doi: 10.1001/archneur.1969.00480120032002.
8
McArdle's myopathy. A report of a case with observations on the muscle ultrastructure.
J Neurol Sci. 1969 Nov-Dec;9(3):515-26. doi: 10.1016/0022-510x(69)90092-6.
9
Amino acid metabolism in McArdle's syndrome.
N Engl J Med. 1973 Apr 12;288(15):774-7. doi: 10.1056/NEJM197304122881507.
10
McArdle's syndrome: a review and a preliminary report of four further cases.麦卡德尔综合征：综述及另外四例病例的初步报告。
Postgrad Med J. 1967 May;43(499):365-71. doi: 10.1136/pgmj.43.499.365.
引用本文的文献
1
Myophosphorylase deficiency (McArdle's disease) in two interrelated families.两个相关家族中的肌磷酸化酶缺乏症（麦卡德尔病）
J Neurol Neurosurg Psychiatry. 1973 Apr;36(2):217-24. doi: 10.1136/jnnp.36.2.217.
2
The histochemical evaluation of the glycogen storage diseases. A review of techniques and their limitations.糖原贮积病的组织化学评估。技术及其局限性综述。
Histochem J. 1970 Sep;2(5):441-50. doi: 10.1007/BF01004725.
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