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Autor:
KcKie, V., KcKie, K. M., Jeraldo, T. L., Adams, R. A., Felice, Alex, Twenty-ninth Annual Meeting of the American Society of Hematology
Five children with homo&ygous sickle cell aneaia without a1sociated alpha thalaasemia receiving partial exchange transfusions designed to maintain the % Hb S between 30-35% for management of LCVV were studied. Ages ranged from 5 11/12 to 13 7/12 year
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3549::2cec3d2f799ec3d48aa31bed5dec0ea7
https://www.um.edu.mt/library/oar/handle/123456789/82315
https://www.um.edu.mt/library/oar/handle/123456789/82315
