性连锁（杜兴氏）肌营养不良症中的血清酶 - Suppr

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Serum enzymes in sex-linked (Duchenne) muscular dystrophy.

作者信息

Shaw R F, Pearson C M, Chowdhury S R, Dreifuss F E

出版信息

Arch Neurol. 1967 Feb;16(2):115-22. doi: 10.1001/archneur.1967.00470200003001.

DOI:10.1001/archneur.1967.00470200003001

PMID:6018043

Abstract

摘要

相似文献

Serum enzymes in sex-linked (Duchenne) muscular dystrophy.性连锁（杜兴氏）肌营养不良症中的血清酶

Arch Neurol. 1967 Feb;16(2):115-22. doi: 10.1001/archneur.1967.00470200003001.

Evidence against the existence of a subclinical form of X-linked Duchenne muscular dystrophy.

J Neurol Sci. 1970 Jun;10(6):523-33. doi: 10.1016/0022-510x(70)90185-1.

Biochemical aspects of genetically determined progressive muscular dystrophies.遗传性进行性肌营养不良的生化方面

Rev Roum Neurol. 1973;10(6):531-7.

[Progressive muscle dystrophy. II. Enzyme activity chages in serum in progressive muscle dystrophy].[进行性肌营养不良。II. 进行性肌营养不良患者血清中的酶活性变化]

Wien Klin Wochenschr. 1971 Feb 19;83(7):109-13.

[Changes in the activity of blood serum enzymes in relatives of children with myopathy].[肌病患儿亲属血清酶活性的变化]

Vopr Med Khim. 1966 Nov-Dec;12(6):600-3.

[Enzymatic activity of the serum in the family of a progressive muscular dystrophy patient].[进行性肌营养不良患者家族中血清的酶活性]

Iryo. 1969 Oct;23(10):1306-11.

Blood enzymes in Duchene's progressive muscular dystrophy and their correlation with the clinical and histological pictures.杜兴氏进行性肌营养不良症中的血液酶及其与临床和组织学表现的相关性。

Acta Med Pol. 1970;11(4):387-93.

Serum enzyme studies in inherited disease of skeletal muscle.

Clin Chim Acta. 1971 Nov;35(1):183-91. doi: 10.1016/0009-8981(71)90310-x.

Serum enzyme alterations in neuromuscular disorders.

JAMA. 1973 Dec 24;226(13):1536-43.

[Effect of drug administration on the child with progressive muscular dystrophy].[药物给药对进行性肌营养不良患儿的影响]

Iryo. 1969 Oct;23(10):1319-27.

引用本文的文献

Glutamate oxaloacetate transaminase (GOT) in the dy2J genotypes of C57BL/6J mice: possible involvement of regulatory defect in muscular dystrophy.C57BL/6J小鼠dy2J基因型中的谷氨酸草酰乙酸转氨酶（GOT）：调节缺陷可能与肌肉萎缩症有关。

Experientia. 1982 Aug 15;38(8):917-8. doi: 10.1007/BF01953652.

[Biochemical, histological and clinical findings in a four-year-old female carrier of benign X-linked muscular dystrophy (Becker type)].

Humangenetik. 1971;11(4):328-35. doi: 10.1007/BF00278661.

[Diagnosis of female carriers of Duchenne's progressive muscular dystrophy using discriminative analysis of various serum enzyme activities].

Klin Wochenschr. 1969 Oct 15;47(20):1099-103. doi: 10.1007/BF01496643.

[Creatine phosphokinase activity in serum of carriers of progressive muscular dystrophy of Duchenne type].[杜兴氏型进行性肌营养不良携带者血清中的肌酸磷酸激酶活性]

Humangenetik. 1969 Oct;8(2):115-33. doi: 10.1007/BF00295835.

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