McArdle's syndrome.
出版信息
Br Med J. 1968 Jun 15;2(5606):640.
Abstract
摘要
相似文献
1
McArdle's syndrome.麦克尔迪氏综合征。
Br Med J. 1968 Jun 15;2(5606):640.
2
[On 8 cases of cramp due to exertion accompanied by tissue enzyme abnormalities].
Rev Neurol (Paris). 1971 Jan;124(1):80-3.
3
[McArdle's disease without typical symptoms].无典型症状的麦克尔迪氏病
Rinsho Shinkeigaku. 1990 Nov;30(11):1247-51.
4
McArdle's syndrome.麦克尔憩室综合征
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[McArdle's syndrome].[麦克尔憩室综合征]
Lakartidningen. 1972 Aug 30;69(36):4005-10.
6
[Myasthenic form of a metabolic myopathy with dystrophic changes due to storage and symptoms resembling McArdle's syndrome (a case report)].[代谢性肌病的肌无力型伴因储存导致的营养不良性改变及类似麦卡德尔综合征的症状（病例报告）]
Psychiatr Neurol Med Psychol (Leipz). 1971 Nov;23(11):650-7.
7
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.
8
McArdle's disease: a review.麦卡德尔病综述
Ann Clin Lab Sci. 1975 Mar-Apr;5(2):115-22.
9
[McArdle's syndrome].[麦克尔憩室综合征]
Zh Nevropatol Psikhiatr Im S S Korsakova. 1973;73(6):820-5.
10
McArdle's disease and anaesthesia: case reports. Review of potential problems and association with malignant hyperthermia.麦克尔迪氏病与麻醉：病例报告。潜在问题及与恶性高热关联的综述。
Acta Anaesthesiol Scand. 2005 Sep;49(8):1077-83. doi: 10.1111/j.1399-6576.2005.00755.x.
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
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.
3
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.
4
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.
5
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.
6
MCARDLE'S DISEASE. HEREDITARY MYOPATHY DUE TO ABSENCE OF MUSCLE PHOSPHORYLASE.
Arch Neurol. 1963 Oct;9:325-42. doi: 10.1001/archneur.1963.00460100013001.
7
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.
8
Intermittent claudication and lateral lumbar disc protrusions.
J Neurol Neurosurg Psychiatry. 1966 Jun;29(3):273-7. doi: 10.1136/jnnp.29.3.273.
9
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。
Q J Med. 1967 Oct;36(144):565-78.
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