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There are 7901205 results for: content related to: Exploring supportive care for individuals affected by Huntington disease and their family caregivers in a community setting

  1. Huntington disease: families’ experiences of healthcare services

    Journal of Advanced Nursing

    Volume 66, Issue 3, March 2010, Pages: 500–510, Heather Skirton, Janet K. Williams, J. Jackson Barnette and Jane S. Paulsen

    Version of Record online : 9 FEB 2010, DOI: 10.1111/j.1365-2648.2009.05217.x

  2. Social System Responses to Huntington Disease

    Family Process

    Volume 28, Issue 1, March 1989, Pages: 59–68, SEYMOUR KESSLER and MAURICE BLOCH

    Version of Record online : 3 AUG 2004, DOI: 10.1111/j.1545-5300.1989.00059.x

  3. The emotional experiences of family carers in Huntington disease

    Journal of Advanced Nursing

    Volume 65, Issue 4, April 2009, Pages: 789–798, Janet K. Williams, Heather Skirton, Jane S. Paulsen, Toni Tripp-Reimer, Lori Jarmon, Meghan McGonigal Kenney, Emily Birrer, Bonnie L. Hennig and Joann Honeyford

    Version of Record online : 18 FEB 2009, DOI: 10.1111/j.1365-2648.2008.04946.x

  4. The dilemma of suicide and Huntington disease

    American Journal of Medical Genetics

    Volume 26, Issue 2, February 1987, Pages: 315–317, Dr. Seymour Kessler and John M. Opitz

    Version of Record online : 2 JUN 2005, DOI: 10.1002/ajmg.1320260209

  5. Family carer personal concerns in Huntington disease

    Journal of Advanced Nursing

    Volume 68, Issue 1, January 2012, Pages: 137–146, Janet K. Williams, Heather Skirton, James Jackson Barnette and Jane S. Paulsen

    Version of Record online : 12 JUN 2011, DOI: 10.1111/j.1365-2648.2011.05727.x

  6. Forgotten person in the huntington disease family

    American Journal of Medical Genetics

    Volume 48, Issue 3, 15 October 1993, Pages: 145–150, Seymour Kessler

    Version of Record online : 7 JUN 2005, DOI: 10.1002/ajmg.1320480306

  7. Estimation of fertility and fitness in Huntington disease in New England

    American Journal of Medical Genetics

    Volume 33, Issue 2, June 1989, Pages: 248–254, Carol A. Mastromauro, Gregory J. Meissen, L. Adrienne Cupples, Dan K. Kiely, Barbara Berkman and Richard H. Myers

    Version of Record online : 5 JUN 2005, DOI: 10.1002/ajmg.1320330222

  8. Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington disease

    American Journal of Medical Genetics Part A

    Volume 119A, Issue 3, 15 June 2003, Pages: 279–282, L. Djoussé, B. Knowlton, M. Hayden, E.W. Almqvist, R. Brinkman, C. Ross, R. Margolis, A. Rosenblatt, A. Durr, C. Dode, P.J. Morrison, A. Novelletto, M. Frontali, R.J.A. Trent, E. McCusker, E. Gómez-Tortosa, D. Mayo, R. Jones, A. Zanko, M. Nance, R. Abramson, O. Suchowersky, J. Paulsen, M. Harrison, Q. Yang, L.A. Cupples, J.F. Gusella, M.E. MacDonald and R.H. Myers

    Version of Record online : 23 APR 2003, DOI: 10.1002/ajmg.a.20190

  9. Suicide and attempted suicide in Huntington disease: Implications for preclinical testing of persons at risk

    American Journal of Medical Genetics

    Volume 24, Issue 2, June 1986, Pages: 305–311, Dr. Lindsay A. Farrer, John M. Opitz and James F. Reynolds

    Version of Record online : 3 JUN 2005, DOI: 10.1002/ajmg.1320240211

  10. You have free access to this content
    Care/Health Services

    Clinical Genetics

    Volume 76, Issue s1, September 2009, Pages: 85–94,

    Version of Record online : 20 AUG 2009, DOI: 10.1111/j.1399-0004.2009.01225.x

  11. The relationship with the ambulance clinicians as experienced by significant others

    Nursing in Critical Care

    Volume 21, Issue 4, July 2016, Pages: e1–e8, Mats Holmberg, Kerstin Forslund, Anna Carin Wahlberg and Ingegerd Fagerberg

    Version of Record online : 9 JAN 2015, DOI: 10.1111/nicc.12144

  12. A new scale to measure family members' perception of community health care services for persons with Huntington disease

    Journal of Evaluation in Clinical Practice

    Volume 16, Issue 3, June 2010, Pages: 470–475, Valmi D. Sousa, Janet K. Williams, Jack J. Barnette and David A. Reed

    Version of Record online : 11 MAR 2010, DOI: 10.1111/j.1365-2753.2009.01144.x

  13. Couples' experiences of predictive testing and living with the risk or reality of Huntington disease: A qualitative study

    American Journal of Medical Genetics Part A

    Volume 126A, Issue 2, 15 April 2004, Pages: 170–182, Fiona Richards

    Version of Record online : 24 OCT 2003, DOI: 10.1002/ajmg.a.20583

  14. Diagnosis of Huntington disease: A model for the stages of psychological response based on experience of a predictive testing program

    American Journal of Medical Genetics

    Volume 47, Issue 3, 1 September 1993, Pages: 368–374, M. Bloch, S. Adam, A. Fuller, B. Kremer, J. P. Welch, S. Wiggins, P. Whyte, M. Huggins, J. Theilmann and M. R. Hayden

    Version of Record online : 7 JUN 2005, DOI: 10.1002/ajmg.1320470314

  15. Individual use of online-consulting for persons affected with eating disorders and their relatives—evaluation of an online consulting service

    European Eating Disorders Review

    Volume 14, Issue 4, July/August 2006, Pages: 218–225, Martin Grunwald and Dorette Wesemann

    Version of Record online : 21 JUN 2006, DOI: 10.1002/erv.712

  16. Impact on couple relationships of predictive testing for Huntington disease: A longitudinal study

    American Journal of Medical Genetics Part A

    Volume 126A, Issue 2, 15 April 2004, Pages: 161–169, Fiona Richards and Katrina Williams

    Version of Record online : 24 OCT 2003, DOI: 10.1002/ajmg.a.20582

  17. You have full text access to this OnlineOpen article
    Balancing needs as a family caregiver in Huntington's disease: a qualitative interview study

    Health & Social Care in the Community

    Volume 23, Issue 5, September 2015, Pages: 569–576, Merete Røthing, Kirsti Malterud and Jan C. Frich

    Version of Record online : 4 DEC 2014, DOI: 10.1111/hsc.12174

  18. You have free access to this content
    Juvenile onset Huntington disease resulting from a very large maternal expansion

    American Journal of Medical Genetics Part A

    Volume 137A, Issue 3, 1 September 2005, Pages: 328–331, F.A. Nahhas, J. Garbern, K.M. Krajewski, B.B. Roa and G.L. Feldman

    Version of Record online : 11 AUG 2005, DOI: 10.1002/ajmg.a.30891

  19. Trafficking in Human Beings: The EU Approach between Border Control, Law Enforcement and Human Rights

    European Law Journal

    Volume 15, Issue 6, November 2009, Pages: 775–790, Sarah H. Krieg

    Version of Record online : 12 NOV 2009, DOI: 10.1111/j.1468-0386.2009.00490.x

  20. Psychosocial impact of predictive testing for Huntington disease on support persons

    American Journal of Medical Genetics

    Volume 96, Issue 3, 12 June 2000, Pages: 353–359, Janet K. Williams, Debra L. Schutte, Patricia A. Holkup, Catherine Evers and Ann Muilenburg

    Version of Record online : 12 JUL 2000, DOI: 10.1002/1096-8628(20000612)96:3<353::AID-AJMG23>3.0.CO;2-9