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Deborah J Sharp

Datos Biográficos

ID3929848
NOMBREDeborah J Sharp
NOMBRESDeborah J
APELLIDOSharp
FIRMASHARP D J
AFILIACIONESUniversity of Bristol
VERIFICADONo
TOTAL DE OBRAS5
TOTAL DE CITAS5
TOTAL COMO AUTOR5
TOTAL COMO EDITOR0
PRIMER AÑO DE PUBLICACIÓN1999
AÑO MÁS RECIENTE DE PUBLICACIÓN2006
ÍNDICE H2
  • Expectations of patients and parents of children with asthma regarding access to complementary therapy information and services via the NHS

    Open Access•A Shaw, Elizabeth Thompson et al.•ARTICLE•Health Expectations•2006

    Objective To explore the expectations of patients and parents of children with asthma regarding access to complementary therapies via the NHS. Methods Fifty semi‐structured interviews with adults and parents of children with asthma, from a range of health‐care settings, including users and non‐users of complementary therapies. Interviews were recorded, transcribed verbatim and the data were analysed thematically. Results Thirty‐one patients were …

  • Factors that contribute to quality of life outcomes prioritised by people with multiple sclerosis

    Open Access•Maggie Somerset, Timothy J Peters et al.•ARTICLE•Quality of Life Research•2003

  • Variables associated with attendance at, and the perceived helpfulness of, meetings for people with multiple sclerosis

    Open Access•Timothy J Peters, Maggie Somerset et al.•ARTICLE•Health & Social Care in the…•2003•Citada por: 2•Referencias: 2

    People who have chronic disabling conditions are frequently advised by health or social care practitioners to attend meetings organised specifically for individuals who have the same or similar health problems. The purpose of the analyses described in the present paper was to ascertain the variables independently associated with attendance at meetings for people with multiple sclerosis (MS), and amongst those who did attend, variables related to …

  • What do people with MS want and expect from health‐care services

    Open Access•Maggie Somerset, Rona Campbell et al.•ARTICLE•Health Expectations•2001

    Objective To determine the health‐care preferences of people with Multiple Sclerosis (MS). Design Cross‐sectional survey using a postal questionnaire comprising standardized measures of health related quality of life (SF‐36) and of depression (BDI) and original questions about issues linked to health‐care, prioritized by people with MS during an earlier qualitative phase. Participants A stratified sample of 318 people with MS in Scotland and Engl…

  • Obstacles on the path to a primary-care led National Health Service

    Open Access•Maggie Somerset, Alex Faulkner et al.•ARTICLE•Social Science & Medicine•1999•Citada por: 3•Referencias: 20

  • Obstacles on the path to a primary-care led National Health Service

    Open Access•Maggie Somerset, Alex Faulkner et al.•ARTICLE•Social Science & Medicine•1999•Citada por: 3•Referencias: 20

  • Variables associated with attendance at, and the perceived helpfulness of, meetings for people with multiple sclerosis

    Open Access•Timothy J Peters, Maggie Somerset et al.•ARTICLE•Health & Social Care in the…•2003•Citada por: 2•Referencias: 2

    People who have chronic disabling conditions are frequently advised by health or social care practitioners to attend meetings organised specifically for individuals who have the same or similar health problems. The purpose of the analyses described in the present paper was to ascertain the variables independently associated with attendance at meetings for people with multiple sclerosis (MS), and amongst those who did attend, variables related to …

  • Obstacles on the path to a primary-care led National Health Service

    Open Access•Maggie Somerset, Alex Faulkner et al.•ARTICLE•Social Science & Medicine•1999•Citada por: 3•Referencias: 20

  • What do people with MS want and expect from health‐care services

    Open Access•Maggie Somerset, Rona Campbell et al.•ARTICLE•Health Expectations•2001

    Objective To determine the health‐care preferences of people with Multiple Sclerosis (MS). Design Cross‐sectional survey using a postal questionnaire comprising standardized measures of health related quality of life (SF‐36) and of depression (BDI) and original questions about issues linked to health‐care, prioritized by people with MS during an earlier qualitative phase. Participants A stratified sample of 318 people with MS in Scotland and Engl…

  • Factors that contribute to quality of life outcomes prioritised by people with multiple sclerosis

    Open Access•Maggie Somerset, Timothy J Peters et al.•ARTICLE•Quality of Life Research•2003

  • Variables associated with attendance at, and the perceived helpfulness of, meetings for people with multiple sclerosis

    Open Access•Timothy J Peters, Maggie Somerset et al.•ARTICLE•Health & Social Care in the…•2003•Citada por: 2•Referencias: 2

    People who have chronic disabling conditions are frequently advised by health or social care practitioners to attend meetings organised specifically for individuals who have the same or similar health problems. The purpose of the analyses described in the present paper was to ascertain the variables independently associated with attendance at meetings for people with multiple sclerosis (MS), and amongst those who did attend, variables related to …

  • Expectations of patients and parents of children with asthma regarding access to complementary therapy information and services via the NHS

    Open Access•A Shaw, Elizabeth Thompson et al.•ARTICLE•Health Expectations•2006

    Objective To explore the expectations of patients and parents of children with asthma regarding access to complementary therapies via the NHS. Methods Fifty semi‐structured interviews with adults and parents of children with asthma, from a range of health‐care settings, including users and non‐users of complementary therapies. Interviews were recorded, transcribed verbatim and the data were analysed thematically. Results Thirty‐one patients were …

Medicine (5 obras) · Family medicine (4 obras) · Nursing (4 obras) · Multiple Sclerosis Research Studies (3 obras) · Psychology (3 obras) · Attendance (2 obras) · Family Support in Illness (2 obras) · Gerontology (2 obras) · Health care (2 obras) · Patient-Provider Communication in Healthcare (2 obras)

Ethnos_APP • Proyecto Open Source • Licencia MIT • Frontend v2.0.0 • Privacidad y Cookies • Documentación de la API: api.ethnos.app/docs • Código de la API: GitHub • DOI: 10.5281/zenodo.17049435 • Código del Frontend: GitHub • DOI: 10.5281/zenodo.17050053 • cruz.rio.br • Expectantes Misericordiae