Showing 1,641 - 1,660 results of 21,342 for search '(( ((significant risks) OR (significant risk)) decrease ) OR ( significant decrease decrease ))', query time: 0.74s Refine Results
  1. 1641

    Diagnostic criteria for Alcoholic cardiomyopathy. by Fei Yan (128878)

    Published 2025
    “…</p><p><b>Results:</b> Globally, ACM burden showed significant declines from 1990 to 2021, with age-standardized rates decreasing by 22.5-37.1% across prevalence, mortality and disability measures. …”
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  4. 1644

    Demographic and ocular features. by Mingxi Shao (10066570)

    Published 2025
    “…</p><p>Results</p><p>In the PCG group, H<sub>2</sub>O<sub>2</sub> and MDA levels were notably higher than in controls (p < 0.001, <i><i>p</i> </i>= 0.020), while TAS levels were significantly lower (p = 0.043). Adjusting for age and gender, the serum TAS (OR = 0.07, 95% CI 0.01–0.85, <i><i>p</i></i> = 0.037), H<sub>2</sub>O<sub>2</sub> (OR = 1.21, 95% CI 1.09–1.35, <i><i>p</i></i> = 0.001) and MDA (OR = 1.17, 95% CI 1.00–1.34, <i><i>p</i></i> = 0.034) were determined to be independent risk/protective factors for PCG. …”
  5. 1645

    Machine learning model to diagnose PCG. by Mingxi Shao (10066570)

    Published 2025
    “…</p><p>Results</p><p>In the PCG group, H<sub>2</sub>O<sub>2</sub> and MDA levels were notably higher than in controls (p < 0.001, <i><i>p</i> </i>= 0.020), while TAS levels were significantly lower (p = 0.043). Adjusting for age and gender, the serum TAS (OR = 0.07, 95% CI 0.01–0.85, <i><i>p</i></i> = 0.037), H<sub>2</sub>O<sub>2</sub> (OR = 1.21, 95% CI 1.09–1.35, <i><i>p</i></i> = 0.001) and MDA (OR = 1.17, 95% CI 1.00–1.34, <i><i>p</i></i> = 0.034) were determined to be independent risk/protective factors for PCG. …”
  6. 1646

    ROC curves of TAS + SOD + MDA to diagnose PCG. by Mingxi Shao (10066570)

    Published 2025
    “…</p><p>Results</p><p>In the PCG group, H<sub>2</sub>O<sub>2</sub> and MDA levels were notably higher than in controls (p < 0.001, <i><i>p</i> </i>= 0.020), while TAS levels were significantly lower (p = 0.043). Adjusting for age and gender, the serum TAS (OR = 0.07, 95% CI 0.01–0.85, <i><i>p</i></i> = 0.037), H<sub>2</sub>O<sub>2</sub> (OR = 1.21, 95% CI 1.09–1.35, <i><i>p</i></i> = 0.001) and MDA (OR = 1.17, 95% CI 1.00–1.34, <i><i>p</i></i> = 0.034) were determined to be independent risk/protective factors for PCG. …”
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  14. 1654

    <b>The moderating effect of financial literacy on risk preferences and time preferences</b> by Calvin Mudzingiri (22188109)

    Published 2025
    “…Additionally, the study concluded that time preferences significantly moderate financial literacy. An increase in financial literacy is associated with a decrease in time preferences, indicating that as financial literacy rises, subjects become more patient. …”
  15. 1655

    电针预处理通过心肌缺血损伤 棕色脂肪组织和 BMP3b/Smad1/5 通路小鼠 by Danying Qian (21730250)

    Published 2025
    Subjects: “…electroacupuncture significantly decreased…”
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  18. 1658

    Discovery of an Orally Active PDE1 Inhibitor for Disease-Modifying Treatment of Postmenopausal Osteoporosis via Dual Anabolic-Antiresorptive Mechanisms by Farman M. Abbasi (22318766)

    Published 2025
    “…Postmenopausal osteoporosis (PMO) is characterized by an imbalance in bone remodeling with increased osteoclast and decreased osteoblast activity, leading to bone loss and higher fracture risk. …”
  19. 1659

    Discovery of an Orally Active PDE1 Inhibitor for Disease-Modifying Treatment of Postmenopausal Osteoporosis via Dual Anabolic-Antiresorptive Mechanisms by Farman M. Abbasi (22318766)

    Published 2025
    “…Postmenopausal osteoporosis (PMO) is characterized by an imbalance in bone remodeling with increased osteoclast and decreased osteoblast activity, leading to bone loss and higher fracture risk. …”
  20. 1660

    Discovery of an Orally Active PDE1 Inhibitor for Disease-Modifying Treatment of Postmenopausal Osteoporosis via Dual Anabolic-Antiresorptive Mechanisms by Farman M. Abbasi (22318766)

    Published 2025
    “…Postmenopausal osteoporosis (PMO) is characterized by an imbalance in bone remodeling with increased osteoclast and decreased osteoblast activity, leading to bone loss and higher fracture risk. …”