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Die Biomedizinkonvention des Europarates : Humanforschung, Transplantationsmedizin, Genetik, Rechtsanalyse und Rechtsvergleich /Radau, Wiltrud Christine. January 2006 (has links) (PDF)
Univ., Diss.--Düsseldorf, 2005. / Literaturverz. S. [387] - 423.
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How to say I'm sorry a study of the Veterans Administration Hospital Association's Apology and Disclosure Program /Carmack, Heather J. January 2008 (has links)
Thesis (Ph.D.)--Ohio University, June, 2008. / Title from PDF t.p. Includes bibliographical references.
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Rechtfertigung und Opferverhalten /Mitsch, Wolfgang. January 2004 (has links) (PDF)
Univ., Habil.-Schr.--Tübingen, 1991. / Literaturverz. S. 641 - 676.
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The costs and benefits of orthodontic treatment patients' values compared to professional judgments : a thesis submitted in partial fulfillment ... for the degree of Master of Science in Orthodontics ... /Iyer, Monisha Gupta. January 2003 (has links)
Thesis (M.S.)--University of Michigan, 2003. / Includes bibliographical references.
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A study of simulation in canon 1101 in light of recent British authors and jurisprudenceServinsky, Michael E. January 2005 (has links)
Thesis (J.C.L.)--Catholic University of America, 1989. / This is an electronic reproduction of TREN, #029-0166. Includes bibliographical references (leaves 99-103).
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Impact of culture on marriage a psychological perspective and canonical implications /Jorgensen, Gerald Thomas. January 1998 (has links)
Thesis (J.C.L.)--Catholic University of America, 1998. / Includes bibliographical references (leaves 78-83).
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Informed consent in obstetric anesthesia the effect of the amount, timing and modality of information on patient satisfaction /Hicks, Michelle B. Wheeler, Maurice B., January 2008 (has links)
Thesis (Ph. D.)--University of North Texas, Dec., 2008. / Title from title page display. Includes bibliographical references.
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Patientenverfügung zur Auftragsklärung für Entscheidungen am Lebensende : Ärztlicher Notfalldienst und Abteilung Innere Medizin Lindenhofspital Bern /Federspiel, Barbara. January 2004 (has links) (PDF)
Masterarbeit, Univ. Bern, 2004. / Masterarbeit Nachdiplomstudium Management im Gesundheitswesen Medizinische, Rechts- und Wirtschaftswissenschaftliche Fakultät der Universität Bern.
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Die Biomedizinkonvention des Europarates : Humanforschung - Transplantationsmedizin - Genetik - Rechtsanalyse und Rechtsvergleich /Radau, Wiltrud Christine. January 2006 (has links)
Thesis (doctoral)--Universität, Düsseldorf, 2005. / Includes bibliographical references (p. [387]-423).
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”Man får lirka”. : En kvalitativ studie om hur omsorgspersonal förhåller sig till samtycke när de arbetar med personer med demens. / “You have to coax”. : A qualitative study regarding how carers relate to consent when working with people with dementia.Bengtsson, Isabelle, Blomberg, Louise January 2018 (has links)
The aim of this study was to get an increased understanding regarding how carers relate to consent while working with people who has dementia. The study asks the following questions: How does the carers understand the concept of consent associated with giving care to people with dementia? What is considered by the carers in connection to consenting to caregiving by people with dementia? And lastly, how does consent mediate between carers and people with dementia? It had a hermeneutic and qualitative scientific approach. The data was collected through three focus groups with carers and then analyzed according to Jens Rennstam and David Wästerfors (2015) method of analysis. The theoretical analysis was performed with three different theoretical aspects called: Scope for action and relationship, Being a client and relational power. The authors of the theoretical aspects were Kerstin Svensson, Eva Johnsson and Leili Laanemets (2014), Roine Johansson (2007), Katarina Jacobsson, Joakim Thelander and David Wästerfors (2010) and also Mats Franzén (2010). The main conclusion of this study was that the carers used body language and had to phrase their questions well towards the people with dementia regarding if they consented to let them help or not. The relationship between carers and the people with dementia was vital - without it consent was very hard to reach.
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