174 related articles for article (PubMed ID: 19465560)
1. Caregiving by teens for family members with Huntington disease.
Williams JK; Ayres L; Specht J; Sparbel K; Klimek ML
J Fam Nurs; 2009 Aug; 15(3):273-94. PubMed ID: 19465560
[TBL] [Abstract][Full Text] [Related]
2. The emotional experiences of family carers in Huntington disease.
Williams JK; Skirton H; Paulsen JS; Tripp-Reimer T; Jarmon L; McGonigal Kenney M; Birrer E; Hennig BL; Honeyford J
J Adv Nurs; 2009 Apr; 65(4):789-98. PubMed ID: 19228233
[TBL] [Abstract][Full Text] [Related]
3. Experiences of teens living in the shadow of Huntington Disease.
Sparbel KJ; Driessnack M; Williams JK; Schutte DL; Tripp-Reimer T; McGonigal-Kenney M; Jarmon L; Paulsen JS
J Genet Couns; 2008 Aug; 17(4):327-35. PubMed ID: 18347962
[TBL] [Abstract][Full Text] [Related]
4. Family carer personal concerns in Huntington disease.
Williams JK; Skirton H; Barnette JJ; Paulsen JS
J Adv Nurs; 2012 Jan; 68(1):137-46. PubMed ID: 21668480
[TBL] [Abstract][Full Text] [Related]
5. The health and well-being of caregivers of children with cerebral palsy.
Raina P; O'Donnell M; Rosenbaum P; Brehaut J; Walter SD; Russell D; Swinton M; Zhu B; Wood E
Pediatrics; 2005 Jun; 115(6):e626-36. PubMed ID: 15930188
[TBL] [Abstract][Full Text] [Related]
6. 'I felt I have grown up as an adult': caregiving experience of children affected by HIV/AIDS in China.
Zhang L; Li X; Kaljee L; Fang X; Lin X; Zhao G; Zhao J; Hong Y
Child Care Health Dev; 2009 Jul; 35(4):542-50. PubMed ID: 19438874
[TBL] [Abstract][Full Text] [Related]
7. Adults' recollections of their experiences as young caregivers of family members with chronic physical illnesses.
Lackey NR; Gates MF
J Adv Nurs; 2001 May; 34(3):320-8. PubMed ID: 11328437
[TBL] [Abstract][Full Text] [Related]
8. Development of the HD-Teen Inventory.
Driessnack M; Williams JK; Barnette JJ; Sparbel KJ; Paulsen JS
Clin Nurs Res; 2012 May; 21(2):213-23. PubMed ID: 21632913
[TBL] [Abstract][Full Text] [Related]
9. Strategies used by teens growing up in families with Huntington disease.
Williams JK; Driessnack M; Barnette JJ; Sparbel KJ; Leserman A; Thompson S; Paulsen JS
J Pediatr Nurs; 2013; 28(5):464-9. PubMed ID: 23531469
[TBL] [Abstract][Full Text] [Related]
10. 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; 23(5):569-76. PubMed ID: 25471490
[TBL] [Abstract][Full Text] [Related]
11. Development of the Huntington disease family concerns and strategies survey from focus group data.
Williams JK; Barnette JJ; Reed D; Sousa VD; Schutte DL; McGonigal-Kenney M; Jarmon L; Phillips E; Tripp-Reimer T; Paulsen JS
J Nurs Meas; 2010; 18(2):83-99. PubMed ID: 20806651
[TBL] [Abstract][Full Text] [Related]
12. [Caregiver burden in relatives of persons with schizophrenia: an overview of measure instruments].
Reine G; Lancon C; Simeoni MC; Duplan S; Auquier P
Encephale; 2003; 29(2):137-47. PubMed ID: 14567165
[TBL] [Abstract][Full Text] [Related]
13. Caregiving Youth Knowledge and Perceptions of Parental End-of-Life Wishes in Huntington's Disease.
Kavanaugh MS; Noh H; Zhang L
J Soc Work End Life Palliat Care; 2016; 12(4):348-365. PubMed ID: 27938026
[TBL] [Abstract][Full Text] [Related]
14. Huntington's disease. Part 3: family aspects of HD.
Aubeeluck A; Moskowitz CB
Br J Nurs; 2008 Mar 13-26; 17(5):328-31. PubMed ID: 18414297
[TBL] [Abstract][Full Text] [Related]
15. Types of strain among family members of individuals with autism spectrum disorder across the lifespan.
Shivers CM; Krizova K; Lee GK
Res Dev Disabil; 2017 Sep; 68():42-51. PubMed ID: 28735161
[TBL] [Abstract][Full Text] [Related]
16. The Impact of Huntington Disease on Family Carers: a Literature Overview.
Domaradzki J
Psychiatr Pol; 2015; 49(5):931-44. PubMed ID: 26688844
[TBL] [Abstract][Full Text] [Related]
17. Family Caregiving for Individuals With Heart Failure: A Scientific Statement From the American Heart Association.
Kitko L; McIlvennan CK; Bidwell JT; Dionne-Odom JN; Dunlay SM; Lewis LM; Meadows G; Sattler ELP; Schulz R; Strömberg A;
Circulation; 2020 Jun; 141(22):e864-e878. PubMed ID: 32349542
[TBL] [Abstract][Full Text] [Related]
18. A comparative study to identify factors of caregiver burden between baby boomers and post baby boomers: a secondary analysis of a US online caregiver survey.
Kim H; Lee S; Cheon J; Hong S; Chang M
BMC Public Health; 2018 May; 18(1):579. PubMed ID: 29720119
[TBL] [Abstract][Full Text] [Related]
19. The nature of caregiving in children of a parent with multiple sclerosis from multiple sources and the associations between caregiving activities and youth adjustment overtime.
Pakenham KI; Cox S
Psychol Health; 2012; 27(3):324-46. PubMed ID: 21678171
[TBL] [Abstract][Full Text] [Related]
20. "No one else sees the difference: "family members' perceptions of changes in persons with preclinical Huntington disease.
Williams JK; Hamilton R; Nehl C; McGonigal-Kenney M; Schutte DL; Sparbel K; Birrer E; Tripp-Reimer T; Friedrich R; Penziner E; Jarmon L; Paulsen J
Am J Med Genet B Neuropsychiatr Genet; 2007 Jul; 144B(5):636-41. PubMed ID: 17219384
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
