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  Vol. 20 No. 4, April 1969 TABLE OF CONTENTS
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Creatine Phosphokinase

Human Fetus and Patients

Ikuo Goto, MD; Mitsutaka Nagamine, MD; Shibanosuke Katsuki, MD

Arch Neurol. 1969;20(4):422-429.

Since this article does not have an abstract, we have provided the first 150 words of the full text PDF and any section headings.

ENZYMES with the same catalytic function but different molecular form are called isozymes. They can be distinguished by electrophoresis, chromatography, immunochemistry, salt fractionation, or by ultracentrifugation. Electrophoresis is most commonly used in clinical laboratories.

Recently, the isozymes of lactic dehydrogenase have been studied in various neuromuscular disorders.1-8 Because creatine phosphokinase (CPK) activity is very low in tissues other than brain and muscle, study of this enzyme might be more specific for muscle disease. Serum CPK assays are used for the diagnosis of neuromuscular disorders and for the detection of the carrier state in Duchenne dystrophy.9-14

Three isozymes of CPK in various organs have been demonstrated by several investigators.15-17 No characteristic abnormality of CPK isozymes in muscle was found in progressive muscular dystrophy or other neuromuscular disorders.15-17 Several attempts have been made to examine the role of CPK activity in the initiation of contractile activity in . . . [Full Text PDF of this Article]


Author Affiliations

Fukuoka, Japan

From the Second Department of Internal Medicine, Faculty of Medicine, Kyushu University, Fukuoka, Japan.


Footnotes

Submitted for publication Aug 6, 1968; accepted Oct 15.

Reprint requests to Second Department of Internal Medicine, Faculty of Medicine, Kyushu University, Fukuoka, Japan (Dr. Goto).



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