Bioethics in human nutrigenomics research: European Nutrigenomics Organisation workshop report
MM Bergmann, M Bodzioch, ML Bonet… - British journal of …, 2006 - cambridge.org
As part of its work on setting standards and establishing guidelines for nutrigenomics
research, the European Nutrigenomics Organisation (NuGO) is developing bioethical …
research, the European Nutrigenomics Organisation (NuGO) is developing bioethical …
Media coverage of ethical issues in predictive genetic testing: a qualitative analysis
B Zimmermann, B Elger, D Shaw - AJOB empirical bioethics, 2019 - Taylor & Francis
Background: Predictive genetic testing (PGT) raises many ethical issues and is of increasing
interest to the general population. Mass media, especially newspapers, are the public's main …
interest to the general population. Mass media, especially newspapers, are the public's main …
La ética en la comunicación del diagnóstico de síndrome de down
T Vargas Aldecoa - Cuadernos de Bioética, 2019 - digiuv.villanueva.edu
La comunicación del diagnóstico de síndrome de Down tiene serias implicaciones éticas ya
que la finalidad del mismo puede ser eugenésica o terapeútica. El objetivo de este artículo …
que la finalidad del mismo puede ser eugenésica o terapeútica. El objetivo de este artículo …
Non‐invasive prenatal screening: Testing motivations and decision making in the low‐risk population
JK Lea, BK Stevens, S Mulligan… - Journal of Genetic …, 2024 - Wiley Online Library
Non‐invasive prenatal screening provides a risk assessment for aneuploidies by utilizing
cell‐free DNA (cfDNA). It is recommended that cell‐free DNA screening (cfDNA screening) …
cell‐free DNA (cfDNA). It is recommended that cell‐free DNA screening (cfDNA screening) …
Non-invasive prenatal testing (NIPT): does the practice discriminate against persons with disabilities?
A Dufner - Journal of Perinatal Medicine, 2021 - degruyter.com
The most well-known goal of non-invasive prenatal testing (NIPT) is still to determine
whether or not a fetus has trisomy 21. Since women often terminate the pregnancy upon a …
whether or not a fetus has trisomy 21. Since women often terminate the pregnancy upon a …
Carrier detection of phenylketonuria in Iranian families by variable number tandem-repeat polymorphism analysis
SM Hosseini Mazinani, J Koochmeshgi… - … Health Journal, 14 (6) …, 2008 - apps.who.int
This study of Iranian families assessed the usefulness of carrier detection of phenylketonuria
by variable number tandem-repeat [ VNTR] polymorphism analysis. We studied 171 people [ …
by variable number tandem-repeat [ VNTR] polymorphism analysis. We studied 171 people [ …
Relationships matter: ethical considerations for returning results to family members of deceased subjects
LC Milner, EY Liu, NA Garrison - The American Journal of …, 2013 - Taylor & Francis
The obligation to return genetic results to the biological relatives of research subjects is an
emerging issue in research ethics. The lack of consensus regarding this type of thirdparty …
emerging issue in research ethics. The lack of consensus regarding this type of thirdparty …
El documento de consentimiento informado para la realización de pruebas genéticas en el ámbito asistencial y en proyectos de investigación
T Pampols, J Rueda, M Milà, D Valverde, N Garín… - Diagnóstico …, 2013 - Elsevier
Las pruebas genéticas (PG) proporcionan resultados que son para toda la vida y que tienen
implicaciones no solo para el individuo sino para la familia, debiendo ir siempre …
implicaciones no solo para el individuo sino para la familia, debiendo ir siempre …
Efectividad y aspectos éticos del asesoramiento genético en Cuba
IAR Betancourt, BM Teruel - Revista Cubana de Salud Pública, 2021 - medigraphic.com
Introducción: El asesoramiento genético constituye el proceso central en el manejo de
trastornos de causa genética, de ahí la importancia de evaluar su efectividad. Objetivo …
trastornos de causa genética, de ahí la importancia de evaluar su efectividad. Objetivo …