la esferocitosis hereditaria y su diagnostico en la practica clinica

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1.- ADDISON CM., BEAMISH M.R., HALES C.R., et al.: An Inmunoradiometric
assay br ferritin in the serum of normal subjects and pa-
tients wirh iron deflciency and ron overload. J Clin Pathol, 1972;
25: 326— 331.
2.- ACRE 1’., ORRINGER E.P., BENNETT \‘.: Oeflcienr red ccii spectrln
in severe, recesively Inheríted spherocytosis. N Eng .1 Mcd, 1982;
306: 1155—1161.
3.- ACRE P., CASELLA J.P., ZINKi-IAM W.H., MC MILLAN C., BEN-
NETT y.: Partial deflciency of ervthrocyte spectrin in hereditary
spherocyrosls. Nature, 1985; 314: 380—383.
4.- ACRE P., ASIMOS A., CASELLA J.F., MC MILLAN C,: Inheritance
patrern and clinical response to splenectomy as a reflection of ery—
throcyte spectrin deficiency In hereditary spherocytosis. N Eng j
Mcd, 1986; 315: 1579—1583,
5.— ACRE 1’., BEN’NETT V.: Cuantitative and functional analyses of
spec¡rin, ankvrin, band 3 and cainodulin in human red cdl membra—
nes. En: SHOHET S.B., MOHANDAS N. (eda.).: Red ccli membranes,
Methods in Henatology, vol. 19, 1~ edición. New York, Churchill Li—
vingstone, Inc., 1988; 3: 95— 129.
6.- ACRE P.: Hereditary spherocytosls, JAMA, 1989; 262: 2887 —2890.
7.- ACRE It: Pardal deficlencles of erythrocyte spectrim in heredltary
spherocytosis, En: ACRE P., PARKER j.C.