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Suzanne Oparil

Researcher at University of Alabama at Birmingham

Publications -  941
Citations -  122414

Suzanne Oparil is an academic researcher from University of Alabama at Birmingham. The author has contributed to research in topics: Blood pressure & Angiotensin II. The author has an hindex of 106, co-authored 885 publications receiving 113983 citations. Previous affiliations of Suzanne Oparil include Michigan State University & Oregon Health & Science University.

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Co-administration of an ACE-inhibitor (moexipril) and hormonal replacement therapy in postmenopausal women.

TL;DR: Moexipril is effective and well tolerated in the treatment of hypertensive, postmenopausal women and can safely be co-administered to hrt, and was well-tolerated by post menopausal women using hrt.
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Masked Uncontrolled Hypertension Is Not Attributable to Medication Nonadherence.

TL;DR: Findings indicate thatMasked uncontrolled hypertension in treated hypertensive patients is not attributable to antihypertensive medication nonadherence, and measurement of urinary drug and drug metabolite levels demonstrates a similarly high level of antihyertensive medication adherence in both MUCH and truly controlled hypertensive Patients.
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Increased Noradrenaline Content of Hypothalamic Nuclei in Association with Worsening of Hypertension after High Sodium Intake in the Young Spontaneously Hypertensive Rat

TL;DR: Observations lend support to the hypothesis that sodium and the sympathetic nervous system have synergistic effects in the pathogenesis of hypertension in the SHR.
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Comparative antihypertensive efficacy of olmesartan: comparison with other angiotensin II receptor antagonists.

TL;DR: Preliminary evidence suggests that olmesartan, an A II receptor blocker currently being evaluated for approval for clinical use, may provide antihypertensive efficacy that is superior to other members of the class.
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Olmesartan/Amlodipine/Hydrochlorothiazide in Obese Participants With Hypertension: A TRINITY Subanalysis

TL;DR: Irrespective of BMI, triple‐combination treatment resulted in greater LS mean reductions in seated diastolic BP (SeBP) and enabled a greater proportion of participants to reach BP goal vs the dual‐ Combination treatments at week 12.