223 related articles for article (PubMed ID: 22081218)
21. Primary health care professionals' experiences with caring for patients with advanced Huntington's disease: a qualitative study.
van Walsem MR; Howe EI; Andelic N; Frich JC
BMC Prim Care; 2024 May; 25(1):155. PubMed ID: 38714964
[TBL] [Abstract][Full Text] [Related]
22. Survey of the Huntington's Disease Patient and Caregiver Community Reveals Most Impactful Symptoms and Treatment Needs.
Simpson JA; Lovecky D; Kogan J; Vetter LA; Yohrling GJ
J Huntingtons Dis; 2016 Dec; 5(4):395-403. PubMed ID: 27983566
[TBL] [Abstract][Full Text] [Related]
23. 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
[TBL] [Abstract][Full Text] [Related]
24. Instruments measuring the disease-specific quality of life of family carers of people with neurodegenerative diseases: a systematic review.
Page TE; Farina N; Brown A; Daley S; Bowling A; Basset T; Livingston G; Knapp M; Murray J; Banerjee S
BMJ Open; 2017 Mar; 7(3):e013611. PubMed ID: 28360239
[TBL] [Abstract][Full Text] [Related]
25. Caregiver burden in chronic mental illness: the role of patient and caregiver characteristics.
Möller-Leimkühler AM; Wiesheu A
Eur Arch Psychiatry Clin Neurosci; 2012 Mar; 262(2):157-66. PubMed ID: 21538092
[TBL] [Abstract][Full Text] [Related]
26. An International Validation of a Clinical Tool to Assess Carers' Quality of Life in Huntington's Disease.
Aubeeluck A; Stupple EJN; Schofield MB; Hughes AC; van der Meer L; Landwehrmeyer B; Ho AK
Front Psychol; 2019; 10():1658. PubMed ID: 31402885
[TBL] [Abstract][Full Text] [Related]
27. Brain, cognitive, and physical disability correlates of decreased quality of life in patients with Huntington's disease.
Junca E; Pino M; Santamaría-García H; Baez S
Qual Life Res; 2023 Jan; 32(1):171-182. PubMed ID: 35978062
[TBL] [Abstract][Full Text] [Related]
28. Validation of the first quality-of-life measurement for patients with Huntington's disease: the Huntington Quality of Life Instrument.
Clay E; De Nicola A; Dorey J; Squitieri F; Aballéa S; Martino T; Tedroff J; Zielonka D; Auquier P; Verny C; Toumi M
Int Clin Psychopharmacol; 2012 Jul; 27(4):208-14. PubMed ID: 22508443
[TBL] [Abstract][Full Text] [Related]
29. Effect of perceived stigmatization on the quality of life among ageing female family carers: a comparison of carers of adults with intellectual disability and carers of adults with mental illness.
Chou YC; Pu CY; Lee YC; Lin LC; Kröger T
J Intellect Disabil Res; 2009 Jul; 53(7):654-64. PubMed ID: 19490349
[TBL] [Abstract][Full Text] [Related]
30. Head and neck cancer and dysphagia; caring for carers.
Patterson JM; Rapley T; Carding PN; Wilson JA; McColl E
Psychooncology; 2013 Aug; 22(8):1815-20. PubMed ID: 23208850
[TBL] [Abstract][Full Text] [Related]
31. Young people's experiences of growing up in a family affected by Huntington's disease.
Forrest Keenan K; Miedzybrodzka Z; van Teijlingen E; McKee L; Simpson SA
Clin Genet; 2007 Feb; 71(2):120-9. PubMed ID: 17250660
[TBL] [Abstract][Full Text] [Related]
32. Facilitators and barriers in caring for a person with Huntington's disease: input for a remote support program.
Daemen MMJ; Boots LMM; Oosterloo M; de Vugt ME; Duits AA
Aging Ment Health; 2024; 28(1):178-187. PubMed ID: 37409463
[TBL] [Abstract][Full Text] [Related]
33. Well-being of family caregivers of persons with late-stage Huntington's disease: lessons in stress and coping.
Roscoe LA; Corsentino E; Watkins S; McCall M; Sanchez-Ramos J
Health Commun; 2009 Apr; 24(3):239-48. PubMed ID: 19415556
[TBL] [Abstract][Full Text] [Related]
34. Tools to measure quality of life and carer burden in informal carers of heart failure patients: a narrative review.
Whittingham K; Barnes S; Gardiner C
Palliat Med; 2013 Jul; 27(7):596-607. PubMed ID: 23442879
[TBL] [Abstract][Full Text] [Related]
35. Quality of life in couples living with Huntington's disease: the role of patients' and partners' illness perceptions.
Kaptein AA; Scharloo M; Helder DI; Snoei L; van Kempen GM; Weinman J; van Houwelingen JC; Roos RA
Qual Life Res; 2007 Jun; 16(5):793-801. PubMed ID: 17375373
[TBL] [Abstract][Full Text] [Related]
36. Psychological distress among carers and the moderating effects of social support.
George ES; Kecmanovic M; Meade T; Kolt GS
BMC Psychiatry; 2020 Apr; 20(1):154. PubMed ID: 32252700
[TBL] [Abstract][Full Text] [Related]
37. 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
[TBL] [Abstract][Full Text] [Related]
38. Patient and caregiver quality of life in Huntington's disease.
Ready RE; Mathews M; Leserman A; Paulsen JS
Mov Disord; 2008 Apr; 23(5):721-6. PubMed ID: 18175350
[TBL] [Abstract][Full Text] [Related]
39. Family carers' experiences of coping with the deaths of adults in home settings: A narrative analysis of carers' relevant background worries.
Thomas C; Turner M; Payne S; Milligan C; Brearley S; Seamark D; Wang X; Blake S
Palliat Med; 2018 May; 32(5):950-959. PubMed ID: 29400619
[TBL] [Abstract][Full Text] [Related]
40. Family carers' experience of caring for an older parent with severe and persistent mental illness.
McCann TV; Bamberg J; McCann F
Int J Ment Health Nurs; 2015 Jun; 24(3):203-12. PubMed ID: 25963281
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
