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Sebastian Porsdam Mann
Researcher at University of Copenhagen
Publications - 17
Citations - 271
Sebastian Porsdam Mann is an academic researcher from University of Copenhagen. The author has contributed to research in topics: Human rights & Health care. The author has an hindex of 7, co-authored 13 publications receiving 192 citations. Previous affiliations of Sebastian Porsdam Mann include University of Cambridge & University of Oxford.
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Journal ArticleDOI
Human Rights-Based Approaches to Mental Health: A Review of Programs.
TL;DR: All studies reviewed suggest that human-rights based approaches can lead to clinical improvements at relatively low costs, and the fact that such approaches can contribute to positive therapeutic outcomes and, potentially, cost savings, is additional reason for their implementation.
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Facilitating the ethical use of health data for the benefit of society: electronic health records, consent and the duty of easy rescue.
TL;DR: It is argued that the duty of easy rescue—the principle that persons should benefit others when this can be done at no or minimal risk to themselves—grounds the removal of consent requirements for minimally risky records-based research.
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The effect of alternate-day caloric restriction on the metabolic consequences of 8 days of bed rest in healthy lean men: a randomized trial.
Nina Majlund Harder-Lauridsen,Signe Tellerup Nielsen,Sebastian Porsdam Mann,Mark Lyngbæk,Fabiana Braga Benatti,Anne Langkilde,Ian Law,Anne-Sophie Wedell-Neergaard,Carsten Thomsen,Kirsten Møller,Kristian Karstoft,Bente Klarlund Pedersen,Rikke Krogh-Madsen +12 more
TL;DR: Alternate-day caloric restriction without overall energy reduction does not ameliorate the metabolic impairment induced in lean men by 8 days of bed rest, and no positive effects emerged from ADCR on these negative health outcomes.
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Blockchain, consent and prosent for medical research
TL;DR: This paper demonstrates how blockchain technologies can be used to further all three of the bioethical principles underlying consent requirements: the autonomy of patients, by giving them much greater control over their data; beneficence, by greatly facilitating medical research efficiency and by reducing biases and opportunities for errors; and justice, by enabling patients with rare or under-researched conditions to pseudonymously aggregate their data for analysis.
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A framework for the ethical assessment of chimeric animal research involving human neural tissue.
TL;DR: It is argued that changes in cognitive abilities are morally relevant to the extent that they increase the capacities that affect the moral status of any entity, including awareness, autonomy, and sociability.