McArdle's syndrome: a review and a preliminary report of four further cases.
作者信息
Salter R H
出版信息
Postgrad Med J. 1967 May;43(499):365-71. doi: 10.1136/pgmj.43.499.365.
Abstract
摘要
相似文献
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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.
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McArdle's syndrome.麦克尔憩室综合征
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Histopathology of McArdle's disease in a family.一个家族中麦卡德尔病的组织病理学
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[McArdle's metabolic myopathy].[麦卡德尔代谢性肌病]
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Biochemical determinations in a recently investigated case of McArdle's disease.近期一例麦克尔迪氏病病例的生化检测
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[Metabolic myopathy (McArdle's syndrome)].[代谢性肌病（麦卡德尔综合征）]
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Glycogen myopathy in adults.成人糖原贮积性肌病
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Variable presentation of the clinical phenotype of McArdle's disease in a kindred harbouring a novel compound genotype in the muscle glycogen phosphorylase gene.在一个肌肉糖原磷酸化酶基因存在新型复合基因型的家族中，麦克尔迪氏病临床表型的可变表现。
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McArdle's disease: three cases in an Australian family.麦卡德尔病：澳大利亚一个家族中的三例病例。
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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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本文引用的文献
1
A FUNCTIONAL DISORDER OF MUSCLE ASSOCIATED WITH THE ABSENCE OF PHOSPHORYLASE.一种与磷酸化酶缺乏相关的肌肉功能障碍。
Proc Natl Acad Sci U S A. 1959 Jun;45(6):791-7. doi: 10.1073/pnas.45.6.791.
2
McArdle's syndrome: phosphorylase-deficient myopathy.麦克尔憩室综合征：磷酸化酶缺乏性肌病。
Lancet. 1962 May 19;1(7238):1045-8. doi: 10.1016/s0140-6736(62)92145-1.
3
Chronic progressive myopathy with myoglobinuria: demonstration of a glycogenolytic defect in the muscle.伴有肌红蛋白尿的慢性进行性肌病：肌肉中糖原分解缺陷的证明
J Clin Invest. 1959 Nov;38(11):2044-58. doi: 10.1172/JCI103983.
4
MCARDLE'S DISEASE PRESENTING AS CONVULSION AND RHABDOMYOLYSIS.
Am J Med. 1965 Jul;39:142-6. doi: 10.1016/0002-9343(65)90254-8.
5
MCARDLE'S SYNDROME WITH PREVIOUSLY UNREPORTED ELECTROCARDIOGRAPHIC AND SERUM ENZYME ABNORMALITIES.
Ann Intern Med. 1965 Feb;62:328-34. doi: 10.7326/0003-4819-62-2-328.
6
A FAMILY STUDY OF PHOSPHORYLASE DEFICIENCY IN MUSCLE.肌肉中磷酸化酶缺乏症的家族研究
Ann Intern Med. 1965 Feb;62:313-27. doi: 10.7326/0003-4819-62-2-313.
7
A CASE OF MCARDLE'S SYNDROME WITH A POSITIVE FAMILY HISTORY.一例具有阳性家族史的麦卡德尔综合征病例。
J Neurol Neurosurg Psychiatry. 1964 Jun;27(3):186-97. doi: 10.1136/jnnp.27.3.186.
8
MCARDLE'S DISEASE. HEREDITARY MYOPATHY DUE TO ABSENCE OF MUSCLE PHOSPHORYLASE.
Arch Neurol. 1963 Oct;9:325-42. doi: 10.1001/archneur.1963.00460100013001.
9
Hereditary absence of muscle phosphorylase (McArdle's syndrome).遗传性肌肉磷酸化酶缺乏症（麦卡德尔综合征）。
N Engl J Med. 1961 Feb 2;264:223-5. doi: 10.1056/NEJM196102022640504.
10
A metabolic myopathy due to absence of muscle phosphorylase.一种由于肌肉磷酸化酶缺乏引起的代谢性肌病。
Am J Med. 1961 Apr;30:502-17. doi: 10.1016/0002-9343(61)90075-4.
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