330 related articles for article (PubMed ID: 20192883)
1. Measuring life quality, physical function and psychological well-being in neurological illness.
O'Doherty LJ; Hickey A; Hardiman O
Amyotroph Lateral Scler; 2010 Oct; 11(5):461-8. PubMed ID: 20192883
[TBL] [Abstract][Full Text] [Related]
2. [Quality of life of patients with amyotrophic lateral sclerosis].
Leirvik A; Liverød M; Holmøy T
Tidsskr Nor Laegeforen; 2006 Oct; 126(19):2520-2. PubMed ID: 17028632
[TBL] [Abstract][Full Text] [Related]
3. The ALSSQOL: balancing physical and nonphysical factors in assessing quality of life in ALS.
Simmons Z; Felgoise SH; Bremer BA; Walsh SM; Hufford DJ; Bromberg MB; David W; Forshew DA; Heiman-Patterson TD; Lai EC; McCluskey L
Neurology; 2006 Nov; 67(9):1659-64. PubMed ID: 17101900
[TBL] [Abstract][Full Text] [Related]
4. Family caregiver quality of life in multiple sclerosis among Kuwaitis: a controlled study.
Alshubaili AF; Ohaeri JU; Awadalla AW; Mabrouk AA
BMC Health Serv Res; 2008 Oct; 8():206. PubMed ID: 18840287
[TBL] [Abstract][Full Text] [Related]
5. Quality of life of patients with amyotrophic lateral sclerosis.
Tramonti F; Bongioanni P; Di Bernardo C; Davitti S; Rossi B
Psychol Health Med; 2012; 17(5):621-8. PubMed ID: 22313252
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. Life can be worth living in locked-in syndrome.
Lulé D; Zickler C; Häcker S; Bruno MA; Demertzi A; Pellas F; Laureys S; Kübler A
Prog Brain Res; 2009; 177():339-51. PubMed ID: 19818912
[TBL] [Abstract][Full Text] [Related]
9. Psychological health in patients with ALS is maintained as physical function declines.
Cupp J; Simmons Z; Berg A; Felgoise SH; Walsh SM; Stephens HE
Amyotroph Lateral Scler; 2011 Jul; 12(4):290-6. PubMed ID: 21294667
[TBL] [Abstract][Full Text] [Related]
10. Impact of depression and disability on quality of life in Iranian patients with multiple sclerosis.
Ayatollahi P; Nafissi S; Eshraghian MR; Kaviani H; Tarazi A
Mult Scler; 2007 Mar; 13(2):275-7. PubMed ID: 17439899
[TBL] [Abstract][Full Text] [Related]
11. The impact of disabilities on quality of life in people with multiple sclerosis.
Wynia K; Middel B; van Dijk JP; De Keyser JH; Reijneveld SA
Mult Scler; 2008 Aug; 14(7):972-80. PubMed ID: 18632779
[TBL] [Abstract][Full Text] [Related]
12. Cross-sectional and longitudinal correlations between disease progression and different health-related quality of life domains in persons with amyotrophic lateral sclerosis.
De Groot IJ; Post MW; van Heuveln T; Van den Berg LH; Lindeman E
Amyotroph Lateral Scler; 2007 Dec; 8(6):356-61. PubMed ID: 18033593
[TBL] [Abstract][Full Text] [Related]
13. Differences in quality of life modalities give rise to needs of individual support in patients with ALS and their next of kin.
Olsson AG; Markhede I; Strang S; Persson LI
Palliat Support Care; 2010 Mar; 8(1):75-82. PubMed ID: 20163763
[TBL] [Abstract][Full Text] [Related]
14. Illness perception and health-related quality of life in multiple sclerosis.
Spain LA; Tubridy N; Kilpatrick TJ; Adams SJ; Holmes AC
Acta Neurol Scand; 2007 Nov; 116(5):293-9. PubMed ID: 17850407
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Factors influencing the health-related quality of life in Hungarian multiple sclerosis patients.
Füvesi J; Bencsik K; Losonczi E; Fricska-Nagy Z; Mátyás K; Mészáros E; Benedek K; Rajda C; Lencsés G; Vécsei L
J Neurol Sci; 2010 Jun; 293(1-2):59-64. PubMed ID: 20394948
[TBL] [Abstract][Full Text] [Related]
17. Coping and quality of life in one hundred and thirty five subjects with multiple sclerosis.
Montel SR; Bungener C
Mult Scler; 2007 Apr; 13(3):393-401. PubMed ID: 17439909
[TBL] [Abstract][Full Text] [Related]
18. Burden of illness of multiple sclerosis: Part II: Quality of life. The Canadian Burden of Illness Study Group.
Can J Neurol Sci; 1998 Feb; 25(1):31-8. PubMed ID: 9532278
[TBL] [Abstract][Full Text] [Related]
19. Factors predicting quality of life in a group of Polish subjects with multiple sclerosis: accounting for functional state, socio-demographic and clinical factors.
Papuć E; Stelmasiak Z
Clin Neurol Neurosurg; 2012 May; 114(4):341-6. PubMed ID: 22137087
[TBL] [Abstract][Full Text] [Related]
20. Quality of life is favorable for most patients with multiple sclerosis: a population-based cohort study.
Pittock SJ; Mayr WT; McClelland RL; Jorgensen NW; Weigand SD; Noseworthy JH; Rodriguez M
Arch Neurol; 2004 May; 61(5):679-86. PubMed ID: 15148144
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
