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Marsha Treadwell

Dados Biográficos

ID7104520
NOMEMarsha Treadwell
PRENOMESMarsha
SOBRENOMETreadwell
ASSINATURATREADWELL M
AFILIAÇÕESUniversity of California, San Francisco
ORCID0000-0003-0521-1846
VERIFICADOSim
TOTAL DE OBRAS5
TOTAL DE CITAÇÕES0
TOTAL COMO AUTOR5
TOTAL COMO EDITOR0
PRIMEIRO ANO DE PUBLICAÇÃO2016
ANO MAIS RECENTE DE PUBLICAÇÃO2024
ÍNDICE H0
  • Genomics and Health Data Governance in Africa

    Open Access•Nchangwi Syntia Munung, Charmaine D Royal et al.•ARTICLE•The Hastings Center Report•2024

    Effectively addressing ethical issues in precision medicine research in Africa requires a holistic social contract that integrates biomedical knowledge with local cultural values and Indigenous knowledge systems. Drawing on African epistemologies such as ubuntu and ujamaa and on our collective experiences in genomics and big data research for sickle cell disease, hearing impairment, and fragile X syndrome and the project Public Understanding of B…

  • Caught between pity, explicit bias, and discrimination

    Open Access•Nchangwi Syntia Munung, Marsha Treadwell et al.•ARTICLE•Quality of Life Research•2023

    The results highlight the importance of challenging stigmatizing narratives on SCD and recognizing that stigmatization represents a social injustice that significantly diminishes the QoL of individuals living with SCD

  • An evaluation of patient-reported outcomes in sickle cell disease within a conceptual model

    Open Access•Marsha Treadwell, Swapandeep Mushiana et al.•ARTICLE•Quality of Life Research•2022

    Study results highlight the importance of the biopsychosocial model to enhance understanding of the needs of this complex population, and to design multi-dimensional approaches for providing more effective interventions to improve outcomes

  • Social and Psychological Factors Associated With Health Care Transition for Young Adults Living With Sickle Cell Disease

    Open Access•Dora Clayton-Jones, Nadine S Matthie et al.•ARTICLE•Journal of Transcultural Nursing•2021

    Introduction: Due to advances in disease management, mortality rates in children with sickle cell disease (SCD) have decreased. However, mortality rates for young adults (YA) increased, and understanding of social and psychological factors is critical. The aim of this study was to explore factors associated with health care transition experiences for YA with SCD. Method: This was a qualitative descriptive study. A 45-minute semistructured intervi…

  • Community engagement to inform the development of a sickle cell counselor training and certification program in Ghana

    Open Access•Kofi A Anie, Marsha Treadwell et al.•ARTICLE•Journal of Community Genetics•2016

Sem obras proeminentes nesta página.

  • Community engagement to inform the development of a sickle cell counselor training and certification program in Ghana

    Open Access•Kofi A Anie, Marsha Treadwell et al.•ARTICLE•Journal of Community Genetics•2016

  • Social and Psychological Factors Associated With Health Care Transition for Young Adults Living With Sickle Cell Disease

    Open Access•Dora Clayton-Jones, Nadine S Matthie et al.•ARTICLE•Journal of Transcultural Nursing•2021

    Introduction: Due to advances in disease management, mortality rates in children with sickle cell disease (SCD) have decreased. However, mortality rates for young adults (YA) increased, and understanding of social and psychological factors is critical. The aim of this study was to explore factors associated with health care transition experiences for YA with SCD. Method: This was a qualitative descriptive study. A 45-minute semistructured intervi…

  • An evaluation of patient-reported outcomes in sickle cell disease within a conceptual model

    Open Access•Marsha Treadwell, Swapandeep Mushiana et al.•ARTICLE•Quality of Life Research•2022

    Study results highlight the importance of the biopsychosocial model to enhance understanding of the needs of this complex population, and to design multi-dimensional approaches for providing more effective interventions to improve outcomes

  • Caught between pity, explicit bias, and discrimination

    Open Access•Nchangwi Syntia Munung, Marsha Treadwell et al.•ARTICLE•Quality of Life Research•2023

    The results highlight the importance of challenging stigmatizing narratives on SCD and recognizing that stigmatization represents a social injustice that significantly diminishes the QoL of individuals living with SCD

  • Genomics and Health Data Governance in Africa

    Open Access•Nchangwi Syntia Munung, Charmaine D Royal et al.•ARTICLE•The Hastings Center Report•2024

    Effectively addressing ethical issues in precision medicine research in Africa requires a holistic social contract that integrates biomedical knowledge with local cultural values and Indigenous knowledge systems. Drawing on African epistemologies such as ubuntu and ujamaa and on our collective experiences in genomics and big data research for sickle cell disease, hearing impairment, and fragile X syndrome and the project Public Understanding of B…

Medicine (5 obras) · Hemoglobinopathies and Related Disorders (4 obras) · Psychiatry (4 obras) · Disease (3 obras) · Family medicine (3 obras) · Gerontology (3 obras) · Iron Metabolism and Disorders (3 obras) · Nursing (3 obras) · Psychology (3 obras) · Public health (3 obras)

Ethnos_APP • Projeto Open Source • Licença MIT • Frontend v2.0.0 • Privacidade e Cookies • Documentação da API: api.ethnos.app/docs • Código da API: GitHub • DOI: 10.5281/zenodo.17049435 • Código do Frontend: GitHub • DOI: 10.5281/zenodo.17050053 • cruz.rio.br • Expectantes Misericordiae