161 related articles for article (PubMed ID: 18803649)
1. Anxiety undermines quality of life in ALS patients and caregivers.
Vignola A; Guzzo A; Calvo A; Moglia C; Pessia A; Cavallo E; Cammarosano S; Giacone S; Ghiglione P; Chiò A
Eur J Neurol; 2008 Nov; 15(11):1231-6. PubMed ID: 18803649
[TBL] [Abstract][Full Text] [Related]
2. A longitudinal study on quality of life and depression in ALS patient-caregiver couples.
Gauthier A; Vignola A; Calvo A; Cavallo E; Moglia C; Sellitti L; Mutani R; Chiò A
Neurology; 2007 Mar; 68(12):923-6. PubMed ID: 17372127
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Neurobehavioral symptoms in ALS are negatively related to caregivers' burden and quality of life.
Chiò A; Vignola A; Mastro E; Giudici AD; Iazzolino B; Calvo A; Moglia C; Montuschi A
Eur J Neurol; 2010 Oct; 17(10):1298-303. PubMed ID: 20402747
[TBL] [Abstract][Full Text] [Related]
5. Religiousness is positively associated with quality of life of ALS caregivers.
Calvo A; Moglia C; Ilardi A; Cammarosano S; Gallo S; Canosa A; Mastro E; Montuschi A; Chiò A
Amyotroph Lateral Scler; 2011 May; 12(3):168-71. PubMed ID: 21348787
[TBL] [Abstract][Full Text] [Related]
6. Existential well-being and spirituality of individuals with amyotrophic lateral sclerosis is related to psychological well-being of their caregivers.
Pagnini F; Lunetta C; Rossi G; Banfi P; Gorni K; Cellotto N; Castelnuovo G; Molinari E; Corbo M
Amyotroph Lateral Scler; 2011 Mar; 12(2):105-8. PubMed ID: 20653520
[TBL] [Abstract][Full Text] [Related]
7. Aggressiveness, sexuality, and obsessiveness in late stages of ALS patients and their effects on caregivers.
Marconi A; Meloni G; Fossati F; Lunetta C; Bastianello S; Melazzini M; Banfi P; Rossi G; Corbo M
Amyotroph Lateral Scler; 2012 Sep; 13(5):452-8. PubMed ID: 22871080
[TBL] [Abstract][Full Text] [Related]
8. A study comparing patients with amyotrophic lateral sclerosis and their caregivers on measures of quality of life, depression, and their attitudes toward treatment options.
Trail M; Nelson ND; Van JN; Appel SH; Lai EC
J Neurol Sci; 2003 May; 209(1-2):79-85. PubMed ID: 12686407
[TBL] [Abstract][Full Text] [Related]
9. Burden, depression, and anxiety in caregivers of people with amyotrophic lateral sclerosis.
Pagnini F; Rossi G; Lunetta C; Banfi P; Castelnuovo G; Corbo M; Molinari E
Psychol Health Med; 2010 Dec; 15(6):685-93. PubMed ID: 21154021
[TBL] [Abstract][Full Text] [Related]
10. Mindfulness as a Protective Factor for the Burden of Caregivers of Amyotrophic Lateral Sclerosis Patients.
Pagnini F; Phillips D; Bosma CM; Reece A; Langer E
J Clin Psychol; 2016 Jan; 72(1):101-11. PubMed ID: 26485696
[TBL] [Abstract][Full Text] [Related]
11. Individual and health-related quality of life assessment in amyotrophic lateral sclerosis patients and their caregivers.
Lo Coco G; Lo Coco D; Cicero V; Oliveri A; Lo Verso G; Piccoli F; La Bella V
J Neurol Sci; 2005 Nov; 238(1-2):11-7. PubMed ID: 16109426
[TBL] [Abstract][Full Text] [Related]
12. ALS patients and caregivers communication preferences and information seeking behaviour.
Chiò A; Montuschi A; Cammarosano S; De Mercanti S; Cavallo E; Ilardi A; Ghiglione P; Mutani R; Calvo A
Eur J Neurol; 2008 Jan; 15(1):55-60. PubMed ID: 18005051
[TBL] [Abstract][Full Text] [Related]
13. Major stressors facing patients with amyotrophic lateral sclerosis (ALS): a survey to identify their concerns and to compare with those of their caregivers.
Trail M; Nelson N; Van JN; Appel SH; Lai EC
Amyotroph Lateral Scler Other Motor Neuron Disord; 2004 Mar; 5(1):40-5. PubMed ID: 15204023
[TBL] [Abstract][Full Text] [Related]
14. Life factors affecting depression and burden in amyotrophic lateral sclerosis caregivers.
Qutub K; Lacomis D; Albert SM; Feingold E
Amyotroph Lateral Scler Frontotemporal Degener; 2014 Jun; 15(3-4):292-7. PubMed ID: 24555470
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Caregivers of patients with amyotrophic lateral sclerosis: investigating quality of life, caregiver burden, service engagement, and patient survival.
Burke T; Galvin M; Pinto-Grau M; Lonergan K; Madden C; Mays I; Carney S; Hardiman O; Pender N
J Neurol; 2017 May; 264(5):898-904. PubMed ID: 28280986
[TBL] [Abstract][Full Text] [Related]
18. Problem solving skills predict quality of life and psychological morbidity in ALS caregivers.
Murphy V; Felgoise SH; Walsh SM; Simmons Z
Amyotroph Lateral Scler; 2009 Jun; 10(3):147-53. PubMed ID: 18618351
[TBL] [Abstract][Full Text] [Related]
19. Caregiver burden and patients' perception of being a burden in ALS.
Chiò A; Gauthier A; Calvo A; Ghiglione P; Mutani R
Neurology; 2005 May; 64(10):1780-2. PubMed ID: 15911811
[TBL] [Abstract][Full Text] [Related]
20. Quality of life in amyotrophic lateral sclerosis patients and caregivers: Impact of assistive communication from early stages.
Londral A; Pinto A; Pinto S; Azevedo L; De Carvalho M
Muscle Nerve; 2015 Dec; 52(6):933-41. PubMed ID: 25808635
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
