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1
Facilitators and barriers of women's participation in HIV clinical research in Switzerland: A qualitative study.
In: HIV medicine, vol. 23, no. 4, pp. 441-447 (2022)
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2
A Therapeutic Relational Agent for Reducing Problematic Substance Use (Woebot): Development and Usability Study.
In: Journal of medical Internet research, vol 23, iss 3 (2021)
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3
New Directions in Treatments Targeting Stroke Recovery.
In: Stroke, vol 49, iss 12 (2018)
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4
Cognitive Working Memory Training (CWMT) in adolescents suffering from Attention-Deficit/Hyperactivity Disorder (ADHD): A controlled trial taking into account concomitant medication effects.
In: Psychiatry research, vol. 269, pp. 79-85 (2018)
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5
Refractory depression: mechanisms and evaluation of radically open dialectical behaviour therapy (RO-DBT) [REFRAMED]: protocol for randomised trial.
Lynch, TR; Whalley, B; Hempel, RJ. - : BMJ Publishing Group, 2015
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6
Painful oral aphthous-like lesions in patient with kidney cancer after target therapy and bisphosphonate administration: a case report of adverse drug reaction.
Mauceri, R; Di Fede, O; Perrone,D. - : Edizioni Minerva Medica, 2015. : country:IT, 2015
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7
Refractory depression: mechanisms and evaluation of radically open dialectical behaviour therapy (RO-DBT) [REFRAMED]: protocol for randomised trial.
Lynch, TR; Whalley, B; Hempel, RJ. - : England, 2015
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8
Atomoxetine improved attention in children and adolescents with attention-deficit/hyperactivity disorder and dyslexia in a 16 week, acute, randomized, double-blind trial
In: PMC (2013)
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9
Innovative solutions to novel drug development in mental health.
In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2013)
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10
Innovative solutions to novel drug development in mental health.
In: Neurosci Biobehav Rev , 37 (10 Pt 1) pp. 2438-2444. (2013) (2013)
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11
An evaluation of the parents under pressure programme: a study protocol for an RCT into its clinical and cost effectiveness
Barlow, Jane; Sembi, Sukhdev; Gardner, Frances. - : BioMed Central, 2013
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12
Research Article ASSESSMENT OF COLLEGE STUDENT’S AWARENESS ABOUT TUBERCULOSIS IN AHMEDNAGAR
In: http://www.ijrdpl.com/docs/5th/6 Res.pdf (2012)
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13
Association between ambulatory 24-hour blood pressure levels and brain volume reduction: a cross-sectional elderly population-based study
In: ISSN: 1524-4563 ; Hypertension (Dallas, Tex. : 1979) ; https://hal.univ-angers.fr/hal-03355591 ; Hypertension (Dallas, Tex. : 1979), 2012, 60 (5), pp.1324-31. ⟨10.1161/hypertensionaha.112.193409⟩ (2012)
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14
Basal insulin and cardiovascular and other outcomes in dysglycemia.
In: New England Journal of Medicine, vol. 367, no. 4, pp. 319-328 (2012)
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15
n-3 fatty acids and cardiovascular outcomes in patients with dysglycemia.
In: New England Journal of Medicine, vol. 367, no. 4, pp. 309-318 (2012)
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16
Cardiorenal end points in a trial of aliskiren for type 2 diabetes.
In: New England Journal of Medicine, vol. 367, no. 23, pp. 2204-2213 (2012)
Abstract: BACKGROUND: This study was undertaken to determine whether use of the direct renin inhibitor aliskiren would reduce cardiovascular and renal events in patients with type 2 diabetes and chronic kidney disease, cardiovascular disease, or both. METHODS: In a double-blind fashion, we randomly assigned 8561 patients to aliskiren (300 mg daily) or placebo as an adjunct to an angiotensin-converting-enzyme inhibitor or an angiotensin-receptor blocker. The primary end point was a composite of the time to cardiovascular death or a first occurrence of cardiac arrest with resuscitation; nonfatal myocardial infarction; nonfatal stroke; unplanned hospitalization for heart failure; end-stage renal disease, death attributable to kidney failure, or the need for renal-replacement therapy with no dialysis or transplantation available or initiated; or doubling of the baseline serum creatinine level. RESULTS: The trial was stopped prematurely after the second interim efficacy analysis. After a median follow-up of 32.9 months, the primary end point had occurred in 783 patients (18.3%) assigned to aliskiren as compared with 732 (17.1%) assigned to placebo (hazard ratio, 1.08; 95% confidence interval [CI], 0.98 to 1.20; P=0.12). Effects on secondary renal end points were similar. Systolic and diastolic blood pressures were lower with aliskiren (between-group differences, 1.3 and 0.6 mm Hg, respectively) and the mean reduction in the urinary albumin-to-creatinine ratio was greater (between-group difference, 14 percentage points; 95% CI, 11 to 17). The proportion of patients with hyperkalemia (serum potassium level, ≥6 mmol per liter) was significantly higher in the aliskiren group than in the placebo group (11.2% vs. 7.2%), as was the proportion with reported hypotension (12.1% vs. 8.3%) (P<0.001 for both comparisons). CONCLUSIONS: The addition of aliskiren to standard therapy with renin-angiotensin system blockade in patients with type 2 diabetes who are at high risk for cardiovascular and renal events is not supported by these data and may even be harmful. (Funded by Novartis; ALTITUDE ClinicalTrials.gov number, NCT00549757.).
Keyword: Aged; Amides/adverse effects; Amides/therapeutic use; Angiotensin Receptor Antagonists/therapeutic use; Angiotensin-Converting Enzyme Inhibitors/therapeutic use; Antihypertensive Agents/adverse effects; Antihypertensive Agents/therapeutic use; Cardiovascular Diseases/epidemiology; Cardiovascular Diseases/mortality; Combination; Diabetes Mellitus; Double-Blind Method; Drug Therapy; Female; Follow-Up Studies; Fumarates/adverse effects; Fumarates/therapeutic use; Humans; Hyperkalemia/chemically induced; Hypokalemia; Kidney Diseases/epidemiology; Kidney Diseases/etiology; Male; Middle Aged; Patient Dropouts; Renin/antagonists & inhibitors; Treatment Failure; Type 2/complications; Type 2/drug therapy
URL: https://serval.unil.ch/notice/serval:BIB_AA678180CBF9
https://doi.org/10.1056/NEJMoa1208799
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17
Crossover trial of subacute computerized aphasia therapy for anomia with the addition of either levodopa or placebo
In: ISSN: 1545-9683 ; Neurorehabilitation and Neural Repair, Vol. 25, No 1 (2011) pp. 43-47 (2011)
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18
Once-yearly zoledronic acid and days of disability, bed rest, and back pain: randomized, controlled HORIZON Pivotal Fracture Trial.
In: Journal of Bone and Mineral Research, vol. 26, no. 5, pp. 984-992 (2011)
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19
Nova Scotia Medical Bulletin 5(4), 1926
Medical Society of Nova Scotia. - : Halifax, Medical Society of Nova Scotia, 2010
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20
Effect of once-yearly zoledronic acid on the spine and hip as measured by quantitative computed tomography: results of the HORIZON Pivotal Fracture Trial.
In: Osteoporosis International, vol. 21, no. 7, pp. 1277-1285 (2010)
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