Not having enough enzyme activity causes platelets to clump together, forming blood clots.
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Sacks FM, Lichtenstein A, Van Horn L, et al.
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Recently, another risk factor for cardiovascular disease has been discovered: a high homocysteine level.
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Median time to disease progression was 5.2Âpopmonths on the Gemzar plus cisplatin arm compared to 3.7Âpopmonths on the cisplatin arm (LogÂpoprank p=0.009, two–sided).
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Fluvoxamine is a known strong inhibitor of CYP1A2 and also inhibits CYP3A4, CYP2C9, and CYP2C19. In a pharmacokinetic study, 40Âpophealthy female subjects received fluvoxamine in escalating doses from 50 to 200Âpopmg per day for 16Âpopdays, with coadministration of alosetron 1Âpopmg on the last day.
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Some isolates, however, can use other receptors on the T-helper cell surface to enter the cell.
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In general, leukemias are classified rather than staged in order to determine the most appropriate therapy.
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Two to 24 hours following the initial dose of study treatment, patients were allowed to use additional treatment for pain response in the form of a second dose of study treatment or other medication.
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An event was considered treatment-emergent if it occurred for the first time or worsened while receiving therapy following baseline evaluation.