Studies on erythrocyte acetylcholinesterase in essential hypertension
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Genetics (clinical),Drug Discovery,Molecular Medicine
Link
http://link.springer.com/content/pdf/10.1007/BF01728352.pdf
Reference32 articles.
1. Auditore JV, Hartmann RC (1959) Paroxysmal nocturnal hemoglobinuria. II. Erythrocyte acetylcholinesterase defect. Am J Med 27:401–410
2. Blumberg A, Marti HR (1972) Red cell metabolism and hemolysis in patients on dialysis. Proc Eur Dial Transplant Assoc 9:91–96
3. Bramley TA, Coleman R, Finean JB (1971) Chemical, enzymological and permeability properties of human erythrocyte ghosts prepared by hypotonic lysis in media of different osmolarities. Biochim Biophys Acta 241:752–769
4. Canessa M, Adragna N, Solomon HS, Connolly TM, Tosteson DC (1980) Increased sodium-lithium countertransport in red cells of patients with essential hypertension. N Engl J Med 302:772–776
5. Coates PM, Simpson NE (1975) Genetic variation in human erythrocyte acetylcholinesterase. Science 175:1466–1467
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