Ethical issues at the interface of clinical care and research practice in pediatric oncology: a narrative review of parents' and physicians' experiences.
about
Innovating consent for pediatric HCT patientsMotivations of children and their parents to participate in drug research: a systematic reviewRecruiting ethnic minority participants to a clinical trial: a qualitative study.Procedure versus process: ethical paradigms and the conduct of qualitative research.Strengths and weaknesses of guideline approaches to safeguard voluntary informed consent of patients within a dependent relationship.Clinical trial network for the promotion of clinical research for rare diseases in Japan: muscular dystrophy clinical trial network.Negotiating decisions during informed consent for pediatric Phase I oncology trialsDoes phase 1 trial enrollment preclude quality end-of-life care? Phase 1 trial enrollment and end-of-life care characteristics in children with cancerA Qualitative Study into Dependent Relationships and Voluntary Informed Consent for Research in Pediatric Oncology.Empirically-derived Knowledge on Adolescent Assent to Pediatric Biomedical Research.Informed Consent in Asymmetrical Relationships: an Investigation into Relational Factors that Influence Room for Reflection.Expectations and experiences of investigators and parents involved in a clinical trial for Duchenne/Becker muscular dystrophy."Matching" consent to purpose: The example of the Matchmaker Exchange.Parents' and Adolescents' Preferences for Intensified or Reduced Treatment in Randomized Lymphoblastic Leukemia Trials.Ethical considerations in placebo-controlled randomised clinical trials.Suggestions from adolescents, young adults, and parents for improving informed consent in phase 1 pediatric oncology trials.Is decision-making capacity an "essentially contested" concept in pediatrics?Decision making in pediatric oncology: Views of parents and physicians in two European countries.Research involving premature infants: timing is everything.Balancing research interests and patient interests: a qualitative study into the intertwinement of care and research in paediatric oncology.Informed Consent in Pediatric Oncology: A Systematic Review of Qualitative LiteratureExploring the Role of Digital Storytelling in Pediatric Oncology Patients’ Perspectives Regarding Diagnosis
P2860
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P2860
Ethical issues at the interface of clinical care and research practice in pediatric oncology: a narrative review of parents' and physicians' experiences.
description
2011 nî lūn-bûn
@nan
2011 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Ethical issues at the interfac ...... ' and physicians' experiences.
@ast
Ethical issues at the interfac ...... ' and physicians' experiences.
@en
Ethical issues at the interfac ...... ' and physicians' experiences.
@nl
type
label
Ethical issues at the interfac ...... ' and physicians' experiences.
@ast
Ethical issues at the interfac ...... ' and physicians' experiences.
@en
Ethical issues at the interfac ...... ' and physicians' experiences.
@nl
prefLabel
Ethical issues at the interfac ...... ' and physicians' experiences.
@ast
Ethical issues at the interfac ...... ' and physicians' experiences.
@en
Ethical issues at the interfac ...... ' and physicians' experiences.
@nl
P2093
P2860
P356
P1433
P1476
Ethical issues at the interfac ...... ' and physicians' experiences.
@en
P2093
Dirk P Engberts
Dorine Bresters
Evert van Leeuwen
Gertjan J L Kaspers
Martine C de Vries
Mirjam Houtlosser
P2860
P2888
P356
10.1186/1472-6939-12-18
P577
2011-09-27T00:00:00Z
P5875
P6179
1031207948