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NEUROLOGY 1981;31:293
© 1981 American Academy of Neurology

Na+ + K+ ATPase of erythrocyte membranes in Duchenne muscular dystrophy

Shiro Mawatari, M.D., Hideki Igisu, M.D., Yoshigoro Kuroiwa, M.D. and Sanji Miyoshino, M.D.

From the Health Administration Center, Kyushu Institute of Technology (Dr. Mawatari), the Department of Neurology (Drs. Mawatari, Igisu, and Kuroiwai, Faculty of Medicine, Kyushu University, Fukuoka, and the National Nishi-Beppu Hospital (Dr. Miyoshino), Beppu City, Ohita, Japan.

We studied the Na+ + K+ ATPase activity of erythrocyte membranes from patients with Duchenne muscular dystrophy (DMD). Samples from patients and controls were obtained at almost the same time on the same day and processed simultaneously. Difference of anticoagulants, extent of washing the red cells, mechanical or osmotic disruption of the cells, presence or absence of EDTA in the washing solution of the ghosts, intentional removal of the peripheral proteins of the membranes, addition of DMD plasma to the assay system, and different temperatures of membrane storage caused no significant differences between DMD and control in Na+ + K+ ATPase or in response of the enzyme to ouabain.

Address correspondence and reprint requests to Dr. Mawatari, Department of Neurology, Neurological Institute, Faculty of Medicine, Kyushu University, Fukuoka 812, Japan.

This work was supported by grants from the Ministry of Health and Welfare, Japan.

Accepted for publication May 20, 1980.




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W. A. Maltese, S. Bressman, S. Fahn, and D. C. De Vivo
Acetylcholinesterase Activity in Patients With Torsion Dystonia: Measurement in Erythrocyte Membranes
Arch Neurol, February 1, 1985; 42(2): 154 - 155.
[Abstract] [PDF]




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