Researchers' perceptions of the ethical implications of pharmacogenomics research with children. - Wikidata - awgldk - TriplyDB

Researchers' perceptions of the ethical implications of pharmacogenomics research with children.

Researchers' perceptions of the ethical implications of pharmacogenomics research with children.

http://www.wikidata.org/entity/Q37466965

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"Who owns your poop?": insights regarding the intersection of human microbiome research and the ELSI aspects of biobanking and related studies Pharmacogenomics and public health.Ethical aspects of human biobanks: a systematic review.Canadian Research Ethics Board Leadership Attitudes to the Return of Genetic Research Results to Individuals and Their Families Pharmacogenomics and adverse drug reactions in children.Stakeholder views on pharmacogenomic testing.Whole exome or genome sequencing: nurses need to prepare families for the possibilities.The 3-I framework: a framework for developing public policies regarding pharmacogenomics (PGx) testing in Canada.On the readiness of physicians for pharmacogenomics testing: an empirical assessment.A review of consent practices and perspectives for pharmacogenetic testing The storage and use of biological tissue samples from minors for research: a focus group study.Attitudes of parents toward the return of targeted and incidental genomic research findings in children

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Researchers' perceptions of the ethical implications of pharmacogenomics research with children.

http://www.wikidata.org/entity/Q37466965

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 10 February 2009

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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Researchers' perceptions of th ...... nomics research with children.

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Researchers' perceptions of th ...... nomics research with children.

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Researchers' perceptions of th ...... nomics research with children.

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Public Health Genomics

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T Silverstein

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P2860

DNA databanks and consent: a suggested policy option involving an authorization model

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Pharmacogenomic data sample collection and storage: ethical issues and policy approaches.

Incidence of adverse drug reactions in paediatric in/out-patients: a systematic review and meta-analysis of prospective studies

Balancing recruitment and protection: children as research subjects.

Ethical dimensions of genetics in pediatric neurology: a look into the future.

Science and society: children and incompetent adults in genetic research: consent and safeguards.

Genotypic approaches to therapy in children: a national active surveillance network (GATC) to study the pharmacogenomics of severe adverse drug reactions in children.

Developmental and pediatric pharmacogenomics.

Guidelines for the ethical conduct of medical research involving children. Royal College of Paediatrics, Child Health: Ethics Advisory Committee.

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191-201

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