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Journal Abstract Search
149 related items for PubMed ID: 18086713
1. The impact of Juvenile Huntington's Disease on the family: the case of a rare childhood condition. Brewer HM, Eatough V, Smith JA, Stanley CA, Glendinning NW, Quarrell OW. J Health Psychol; 2008 Jan; 13(1):5-16. PubMed ID: 18086713 [Abstract] [Full Text] [Related]
2. The personal experience of juvenile Huntington's disease: an interpretative phenomenological analysis of parents' accounts of the primary features of a rare genetic condition. Smith JA, Brewer HM, Eatough V, Stanley CA, Glendinning NW, Quarrell OW. Clin Genet; 2006 Jun; 69(6):486-96. PubMed ID: 16712700 [Abstract] [Full Text] [Related]
3. Caring for a child with Juvenile Huntington's Disease: helpful and unhelpful support. Brewer HM, Smith JA, Eatough V, Stanley CA, Glendinning NW, Quarrell OW. J Child Health Care; 2007 Mar; 11(1):40-52. PubMed ID: 17287223 [Abstract] [Full Text] [Related]
4. Exploring supportive care for individuals affected by Huntington disease and their family caregivers in a community setting. Soltysiak B, Gardiner P, Skirton H. J Clin Nurs; 2008 Apr; 17(7B):226-34. PubMed ID: 18578798 [Abstract] [Full Text] [Related]
5. The experiences of family members of persons with Huntington's disease. Semple OD. Perspectives; 1995 Apr; 19(4):4-10. PubMed ID: 8571758 [No Abstract] [Full Text] [Related]
7. Avoidance as a strategy of (not) coping: qualitative interviews with carers of Huntington's Disease patients. Lowit A, van Teijlingen ER. BMC Fam Pract; 2005 Sep 14; 6():38. PubMed ID: 16162290 [Abstract] [Full Text] [Related]
8. Huntington's disease. Part 2: treatment and management issues in juvenile HD. Aubeeluck A, Brewer H. Br J Nurs; 2005 Sep 14; 17(4):260-3. PubMed ID: 18414272 [Abstract] [Full Text] [Related]
9. [Working with families in the early stages of psychosis: a structured intervention for caregivers]. Alpi A, Cocchi A, Meneghelli A, Pafumi N, Patelli G. G Ital Med Lav Ergon; 2008 Sep 14; 30(3 Suppl B):B62-70. PubMed ID: 19288779 [Abstract] [Full Text] [Related]
10. Huntington's disease--falling through the net. Shakespeare J, Anderson J. Health Trends; 1993 Sep 14; 25(1):19-23. PubMed ID: 10125696 [Abstract] [Full Text] [Related]
11. Communication and Huntington's disease: qualitative interviews and focus groups with persons with Huntington's disease, family members, and carers. Hartelius L, Jonsson M, Rickeberg A, Laakso K. Int J Lang Commun Disord; 2010 Sep 14; 45(3):381-93. PubMed ID: 20144006 [Abstract] [Full Text] [Related]
12. Balancing needs as a family caregiver in Huntington's disease: a qualitative interview study. Røthing M, Malterud K, Frich JC. Health Soc Care Community; 2015 Sep 14; 23(5):569-76. PubMed ID: 25471490 [Abstract] [Full Text] [Related]
13. Alzheimer's disease and the psychosocial burden for caregivers. Gruffydd E, Randle J. Community Pract; 2006 Jan 14; 79(1):15-8. PubMed ID: 16435497 [Abstract] [Full Text] [Related]
14. Fathers' views and understanding of their roles in families with a child with acute lymphoblastic leukaemia: an interpretative phenomenological analysis. Hill K, Higgins A, Dempster M, McCarthy A. J Health Psychol; 2009 Nov 14; 14(8):1268-80. PubMed ID: 19858345 [Abstract] [Full Text] [Related]
18. Caregiver roles in families affected by Huntington's disease: a qualitative interview study. Røthing M, Malterud K, Frich JC. Scand J Caring Sci; 2014 Dec 14; 28(4):700-5. PubMed ID: 24237139 [Abstract] [Full Text] [Related]
19. Care and secrecy: being a mother of children living with HIV in Burkina Faso. Hejoaka F. Soc Sci Med; 2009 Sep 14; 69(6):869-76. PubMed ID: 19540644 [Abstract] [Full Text] [Related]
20. "Other cancer survivors": the impact on family and caregivers. Golant M, Haskins NV. Cancer J; 2008 Sep 14; 14(6):420-4. PubMed ID: 19060608 [Abstract] [Full Text] [Related] Page: [Next] [New Search]