263 related articles for article (PubMed ID: 31747791)
1. Psychological distress in partners of patients with amyotrophic lateral sclerosis and progressive muscular atrophy: what's the role of care demands and perceived control?
de Wit J; Beelen A; van den Heerik MS; van den Berg LH; Visser-Meily JMA; Schröder CD
Psychol Health Med; 2020 Mar; 25(3):319-330. PubMed ID: 31747791
[TBL] [Abstract][Full Text] [Related]
2. A blended psychosocial support program for partners of patients with amyotrophic lateral sclerosis and progressive muscular atrophy: protocol of a randomized controlled trial.
de Wit J; Beelen A; Drossaert CHC; Kolijn R; van den Berg LH; Visser-Meily JMA; Schröder CD
BMC Psychol; 2018 May; 6(1):20. PubMed ID: 29716660
[TBL] [Abstract][Full Text] [Related]
3. User perspectives on a psychosocial blended support program for partners of patients with amyotrophic lateral sclerosis and progressive muscular atrophy: a qualitative study.
de Wit J; Vervoort SCJM; van Eerden E; van den Berg LH; Visser-Meily JMA; Beelen A; Schröder CD
BMC Psychol; 2019 Jun; 7(1):35. PubMed ID: 31202270
[TBL] [Abstract][Full Text] [Related]
4. Blended psychosocial support for partners of patients with ALS and PMA: results of a randomized controlled trial.
De Wit J; Beelen A; Drossaert CHC; Kolijn R; Van Den Berg LH; SchrÖder CD; Visser-Meily JMA
Amyotroph Lateral Scler Frontotemporal Degener; 2020 Aug; 21(5-6):344-354. PubMed ID: 32362155
[No Abstract] [Full Text] [Related]
5. Coping strategies and psychological distress in caregivers of patients with Amyotrophic Lateral Sclerosis (ALS).
Siciliano M; Santangelo G; Trojsi F; Di Somma C; Patrone M; Femiano C; Monsurrò MR; Trojano L; Tedeschi G
Amyotroph Lateral Scler Frontotemporal Degener; 2017 Aug; 18(5-6):367-377. PubMed ID: 28631956
[TBL] [Abstract][Full Text] [Related]
6. Patients' self-perceived burden, caregivers' burden and quality of life for amyotrophic lateral sclerosis patients: a cross-sectional study.
Geng D; Ou R; Miao X; Zhao L; Wei Q; Chen X; Liang Y; Shang H; Yang R
J Clin Nurs; 2017 Oct; 26(19-20):3188-3199. PubMed ID: 27874996
[TBL] [Abstract][Full Text] [Related]
7. Longitudinal predictors of caregiver burden in amyotrophic lateral sclerosis: a population-based cohort of patient-caregiver dyads.
Burke T; Hardiman O; Pinto-Grau M; Lonergan K; Heverin M; Tobin K; Staines A; Galvin M; Pender N
J Neurol; 2018 Apr; 265(4):793-808. PubMed ID: 29396678
[TBL] [Abstract][Full Text] [Related]
8. Caregiver burden in amyotrophic lateral sclerosis is more dependent on patients' behavioral changes than physical disability: a comparative study.
Lillo P; Mioshi E; Hodges JR
BMC Neurol; 2012 Dec; 12():156. PubMed ID: 23216745
[TBL] [Abstract][Full Text] [Related]
9. Psychological distress and coping styles of caregivers of patients with amyotrophic lateral sclerosis: a longitudinal study.
de Wit J; Bakker LA; van Groenestijn AC; Baardman JF; van den Berg LH; Visser-Meily JMA; SchrÖder CD
Amyotroph Lateral Scler Frontotemporal Degener; 2019 May; 20(3-4):235-241. PubMed ID: 30654658
[No Abstract] [Full Text] [Related]
10. Caregiving in ALS - a mixed methods approach to the study of Burden.
Galvin M; Corr B; Madden C; Mays I; McQuillan R; Timonen V; Staines A; Hardiman O
BMC Palliat Care; 2016 Sep; 15(1):81. PubMed ID: 27596749
[TBL] [Abstract][Full Text] [Related]
11. Depression and anxiety in amyotrophic lateral sclerosis: correlations between the distress of patients and caregivers.
Chen D; Guo X; Zheng Z; Wei Q; Song W; Cao B; Huang R; Yang R; Shang H
Muscle Nerve; 2015 Mar; 51(3):353-7. PubMed ID: 24976369
[TBL] [Abstract][Full Text] [Related]
12. Mutual support groups for family caregivers of people with amyotrophic lateral sclerosis in Italy: A pilot study.
Cipolletta S; Gammino GR; Francescon P; Palmieri A
Health Soc Care Community; 2018 Jul; 26(4):556-563. PubMed ID: 29479773
[TBL] [Abstract][Full Text] [Related]
13. Informal Caregiving in Amyotrophic Lateral Sclerosis (ALS): A High Caregiver Burden and Drastic Consequences on Caregivers' Lives.
Schischlevskij P; Cordts I; Günther R; Stolte B; Zeller D; Schröter C; Weyen U; Regensburger M; Wolf J; Schneider I; Hermann A; Metelmann M; Kohl Z; Linker RA; Koch JC; Stendel C; Müschen LH; Osmanovic A; Binz C; Klopstock T; Dorst J; Ludolph AC; Boentert M; Hagenacker T; Deschauer M; Lingor P; Petri S; Schreiber-Katz O
Brain Sci; 2021 Jun; 11(6):. PubMed ID: 34200087
[TBL] [Abstract][Full Text] [Related]
14. Resilience and distress among amyotrophic lateral sclerosis patients and caregivers.
Rabkin JG; Wagner GJ; Del Bene M
Psychosom Med; 2000; 62(2):271-9. PubMed ID: 10772408
[TBL] [Abstract][Full Text] [Related]
15. Impact of disease, cognitive and behavioural factors on caregiver outcome in amyotrophic lateral sclerosis.
Watermeyer TJ; Brown RG; Sidle KC; Oliver DJ; Allen C; Karlsson J; Ellis C; Shaw CE; Al-Chalabi A; Goldstein LH
Amyotroph Lateral Scler Frontotemporal Degener; 2015; 16(5-6):316-23. PubMed ID: 26199108
[TBL] [Abstract][Full Text] [Related]
16. Impact of patient suffering on caregiver well-being: the case of amyotrophic lateral sclerosis patients and their caregivers.
Boerner K; Mock SE
Psychol Health Med; 2012; 17(4):457-66. PubMed ID: 22117117
[TBL] [Abstract][Full Text] [Related]
17. The Evolution of Caregiver Burden in Frontotemporal Dementia with and without Amyotrophic Lateral Sclerosis.
Hsieh S; Leyton CE; Caga J; Flanagan E; Kaizik C; O'Connor CM; Kiernan MC; Hodges JR; Piguet O; Mioshi E
J Alzheimers Dis; 2016; 49(3):875-85. PubMed ID: 26519438
[TBL] [Abstract][Full Text] [Related]
18. Caregiver burden in amyotrophic lateral sclerosis: A systematic review.
de Wit J; Bakker LA; van Groenestijn AC; van den Berg LH; Schröder CD; Visser-Meily JMA; Beelen A
Palliat Med; 2018 Jan; 32(1):231-245. PubMed ID: 28671483
[TBL] [Abstract][Full Text] [Related]
19. Experiences of burden, needs, rewards and resilience in family caregivers of people living with Motor Neurone Disease/Amyotrophic Lateral Sclerosis: A secondary thematic analysis of qualitative interviews.
Weisser FB; Bristowe K; Jackson D
Palliat Med; 2015 Sep; 29(8):737-45. PubMed ID: 25762578
[TBL] [Abstract][Full Text] [Related]
20. Participation and mental well-being of mothers of home-living patients with spinal muscular atrophy.
Cremers CH; Fischer MJ; Kruitwagen-van Reenen ET; Wadman RI; Vervoordeldonk JJ; Verhoef M; Visser-Meily JM; van der Pol WL; Schröder CD
Neuromuscul Disord; 2019 Apr; 29(4):321-329. PubMed ID: 30954388
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
