Effects of HFCS and hazelnut on food intake, liquid intake and body weights in groups of rats. by Ayça Toprak-Semiz (22582110)

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Effects of HFCS and hazelnut on biochemical parameters in groups of rats. by Ayça Toprak-Semiz (22582110)

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This is the raw data used for this study. by James M. Friedman (22522150)

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Pre-operative versus post-operative symptoms. by James M. Friedman (22522150)

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The Human Disharmony Loop (full) Including Inciting Factors. by James M. Friedman (22522150)

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Baseline Severity of Disease by Scapular Dyskinesia Stage^1. by James M. Friedman (22522150)

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The Human Disharmony Loop Clinical Presentation. by James M. Friedman (22522150)

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Patient Demographics. by James M. Friedman (22522150)

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Pain and Function Outcomes Following PM Tenotomy. by James M. Friedman (22522150)

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Diagnostic Criteria for Human Disharmony Loop. by James M. Friedman (22522150)

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Normal Anatomy vs. Disharmonic Pathoanatomy. by James M. Friedman (22522150)

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The Human Disharmony Loop (central). by James M. Friedman (22522150)

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Sample Pain Diagrams. by James M. Friedman (22522150)

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Summary of study eligibility criteria. by Biban Gill (1473337)

“…Considering the high prevalence of BV among African, Caribbean and Black (ACB) women, we conducted a prospective, randomized, open-label phase 1 clinical trial to determine the feasibility, safety and tolerability of administering low-dose estrogen, probiotics or both in combination to improve vaginal health and decrease HIV-1 susceptibility.</p><p>Methods</p><p>ACB women aged 18–49 from the Greater Toronto Area (GTA) were randomized to one of four study arms: intravaginal estradiol (Estring©; 7.5mg/day); a vaginal probiotic (RepHresh™ Pro-B™) administered twice daily; a combination of Estring© and vaginal RepHresh™ Pro-B™ (twice daily); or the Estring© and oral RepHresh™ Pro-B™ (twice daily), for a duration of 30 days. …”

Summary of study participation and feasibility. by Biban Gill (1473337)

“…Considering the high prevalence of BV among African, Caribbean and Black (ACB) women, we conducted a prospective, randomized, open-label phase 1 clinical trial to determine the feasibility, safety and tolerability of administering low-dose estrogen, probiotics or both in combination to improve vaginal health and decrease HIV-1 susceptibility.</p><p>Methods</p><p>ACB women aged 18–49 from the Greater Toronto Area (GTA) were randomized to one of four study arms: intravaginal estradiol (Estring©; 7.5mg/day); a vaginal probiotic (RepHresh™ Pro-B™) administered twice daily; a combination of Estring© and vaginal RepHresh™ Pro-B™ (twice daily); or the Estring© and oral RepHresh™ Pro-B™ (twice daily), for a duration of 30 days. …”

Sociodemographic and economic factors of study subjects, Ethiopia, EDHS 2005–2016 (N = 29,525). by Girma Beressa (9580436)

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Multivariable multilevel mixed-effects logistic regression analyses of zinc utilisation and predictors among under-five children with diarrhoea, Ethiopia, 2005–2016 (N = 29,525). by Girma Beressa (9580436)

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Pairwise comparison of adult longevity across treatments. P-values from pairwise comparisons between control conditions and irradiation doses. Values in boldface indicate significa... by Flavia Cerasti (21655934)

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Detecting neural spikes by thresholding. by Ariel Burman (20329776)

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Dynamical changes in the buffer population (<i>L</i> = 1023). by Ariel Burman (20329776)

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