[进行性肌营养不良症的酶活性测定。IV. 杜兴型在生命最初2年临床前期的血清酶动力学] - Suppr

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超能文献

[Enzyme activity determination in progressive muscular dystrophy. IV. Serum enzymatic kinetics in the preclinical stage of the Duchenne type during the 1st 2 years of life].

作者信息

Heyck H, Laudahn G, Carsten P M

出版信息

Klin Wochenschr. 1966 Jun 15;44(12):695-700. doi: 10.1007/BF01790793.

DOI:10.1007/BF01790793

PMID:5990806

Abstract

摘要

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[Enzyme activity determination in progressive muscular dystrophy. IV. Serum enzymatic kinetics in the preclinical stage of the Duchenne type during the 1st 2 years of life].[进行性肌营养不良症的酶活性测定。IV. 杜兴型在生命最初2年临床前期的血清酶动力学]

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本文引用的文献

Histopathological features of muscle in the preclinical stages of muscular dystrophy.肌肉营养不良临床前期阶段肌肉的组织病理学特征。

Brain. 1962 Mar;85:109-20. doi: 10.1093/brain/85.1.109.

Studies of enzymes in serum in muscular dystrophy. II. Diagnostic and prognostic significance in relatives of dystrophic persons.肌营养不良症患者血清中酶的研究。II. 对肌营养不良症患者亲属的诊断及预后意义。

Pediatrics. 1961 Dec;28:962-70.

Activity of glutamic-oxalacetic transminase and lactic dehydrogenase in cerebrospinal fluid and plasma of normal and abnormal newborn infants.正常和异常新生儿脑脊液及血浆中谷草转氨酶和乳酸脱氢酶的活性

Pediatrics. 1959 Sep;24:378-88.

A comparative study of fetal and maternal serum enzyme levels.

J Lab Clin Med. 1959 Sep;54:417-26.

[CLINICAL AND BIOCHEMICAL STUDIES IN MYOPATHIES. 3. RECESSIVE X-CHROMOSOMAL MUSCULAR DYSTROPHY WITH RELATIVELY BENIGN COURSE].[肌病的临床与生化研究。3. 具有相对良性病程的隐性X染色体连锁型肌营养不良症]

Klin Wochenschr. 1965 Feb 1;43:158-63. doi: 10.1007/BF01484508.

MUSCULAR DYSTROPHY: SOME RECENT ADVANCES IN KNOWLEDGE.肌肉萎缩症：知识领域的一些最新进展

Br Med J. 1964 May 16;1(5393):1271-4 CONTD. doi: 10.1136/bmj.1.5393.1271.

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Lancet. 1964 Feb 29;1(7331):447-52. doi: 10.1016/s0140-6736(64)90792-5.

MUSCULAR DYSTROPHY. REVIEW AND RECENT OBSERVATIONS.肌肉萎缩症。综述与近期观察

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