BACKGROUND: The antiproteinuric pharmacokinetics of Ramipril in response to different doses and modalities of administration has been poorly investigated so far. STUDY DESIGN: Prospective, open-label and not placebo controlled study. SETTING AND PARTICIPANTS: 40 Caucasian adult patients having GFR >/= 50 mL/min, proteinuria 1-3 g/day; SBP/DBP

How to improve duration and efficiency of the antiproteinuric response to Ramipril: RamiPROT-a prospective cohort study

Fuiano G;FOTI D
2017-01-01

Abstract

BACKGROUND: The antiproteinuric pharmacokinetics of Ramipril in response to different doses and modalities of administration has been poorly investigated so far. STUDY DESIGN: Prospective, open-label and not placebo controlled study. SETTING AND PARTICIPANTS: 40 Caucasian adult patients having GFR >/= 50 mL/min, proteinuria 1-3 g/day; SBP/DBP
2017
Adult; Aged; Angiotensin conventing enzyme inhibitors
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.12317/11890
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