يعرض 1 - 10 نتائج من 1,810 نتيجة بحث عن '"Pickkers Peter"', وقت الاستعلام: 1.62s تنقيح النتائج
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    المساهمون: University of California San Francisco (UC San Francisco), University of California (UC), University of Alberta, University of Washington Seattle, University of Florida Gainesville (UF), Perelman School of Medicine, University of Pennsylvania, Wake Forest School of Medicine Winston-Salem, Wake Forest Baptist Medical Center, University of Pittsburgh School of Medicine, Pennsylvania Commonwealth System of Higher Education (PCSHE), University of Chicago, PAIR (Palliative and Advanced Illness Research) Center, Alberta Health Services Calgary, University Hospital Münster - Universitaetsklinikum Muenster Germany (UKM), SeaStar Medical, Department of Medicine San Francisco, University of California (UC)-University of California (UC), University of California San Diego (UC San Diego), Radboud University Medical Center Nijmegen, Division of Chronic Care Management, Centers for Medicare & Medicaid Services, AM-Pharma, University of New South Wales Sydney (UNSW), French-Clinical Research Infrastructure Network - F-CRIN Paris (Cardiovascular & Renal Clinical Trialists - CRCT ), Centre d'investigation clinique Nancy (CIC), Centre Hospitalier Régional Universitaire de Nancy (CHRU Nancy)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lorraine (UL), Centre Hospitalier Princesse Grace, Guy's and St Thomas' Hospital London, King‘s College London

    المصدر: ISSN: 1364-8535.

    مصطلحات موضوعية: [SDV]Life Sciences [q-bio]

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    دورية أكاديمية

    المساهمون: HUS Perioperative, Intensive Care and Pain Medicine, Department of Diagnostics and Therapeutics, Clinicum

    وصف الملف: application/pdf

    العلاقة: This work was supported by AM-Pharma. The role of the sponsor in the design of the study was to coordinate and facilitate processes, where the scientific input was provided by the members of the protocol committee, steering committee, and specific input by external experts in data management and statistics. The sponsor contracted an external contract research organization to operationally conduct the study at the study sites. The contract research organization was responsible for setting up the technical systems, data collection, quality control, pharmacovigilance, statistics, and further overall management of the study, under coordination and supervision of the sponsor. The statistical analysis plan was prepared by the contract research organization with input by principal investigator, sponsor, and external experts in statistics. The analyses were performed by external contract research organizations. Data were interpreted by the members of the steering committee, and, in a later phase, all coauthors and external experts, coordinated by the sponsor, could provide input. The principal investigator was responsible for preparation of the manuscript. All coauthors reviewed, made adjustments, and approved the manuscript. The decision to submit the manuscript was made by the principal investigator and other coauthors.; the REVIVAL investigators , Pickkers , P , Angus , D C , Bass , K & Pettilä , V 2024 , ' Phase-3 trial of recombinant human alkaline phosphatase for patients with sepsis-associated acute kidney injury (REVIVAL) ' , Intensive Care Medicine , vol. 50 , pp. 68–78 . https://doi.org/10.1007/s00134-023-07271-wTest; http://hdl.handle.net/10138/570610Test; 873c068f-9b86-4137-9cea-2d51a3e6e285; 001135595300006

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    المصدر: Critical Care. 25(1)

    وصف الملف: application/pdf

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