A study comparing patients with amyotrophic lateral sclerosis and their caregivers on measures of quality of life, depression, and their attitudes toward treatment options.
about
Severe loss of appetite in amyotrophic lateral sclerosis patients: online self-assessment studyDrug therapy for pain in amyotrophic lateral sclerosis or motor neuron diseaseDrug therapy for pain in amyotrophic lateral sclerosis or motor neuron diseaseEvaluation of quality of life in individuals with severe chronic motor disability: A major challengePatient-Perceived Outcomes and Quality of Life in ALSComprehensive rehabilitative care across the spectrum of amyotrophic lateral sclerosis.Is dignity therapy feasible to enhance the end of life experience for people with motor neurone disease and their family carers?Prevalence of depressive disorders and change over time in late-stage ALS.Determinants of accepting non-invasive ventilation treatment in motor neurone disease: a quantitative analysis at point of needCaregiver burden in amyotrophic lateral sclerosis is more dependent on patients' behavioral changes than physical disability: a comparative study.A survey on self-assessed well-being in a cohort of chronic locked-in syndrome patients: happy majority, miserable minorityCaregiving in ALS - a mixed methods approach to the study of BurdenRespiratory function of people with amyotrophic lateral sclerosis and caregiver distress level: a correlational study.Conjugal amyotrophic lateral sclerosis: a case report from ScotlandAttitudes Toward Assisted Suicide and Life-Prolonging Measures in Swiss ALS Patients and Their Caregivers.A Review: carers, MND and service provision.Family caregiver perspectives on caring for ventilator-assisted individuals at homePsychological health in patients with amyotrophic lateral sclerosis.Usage of support services in primary lateral sclerosis.Quality of life in amyotrophic lateral sclerosis/motor neuron disease: a structured review.The impact on the family carer of motor neurone disease and intervention with noninvasive ventilation.A comparison of pharmacy students' and active older adults' perceptions regarding geriatric quality of life.A 10-year literature review of family caregiving for motor neurone disease: moving from caregiver burden studies to palliative care interventions.Depression and disease progression in amyotrophic lateral sclerosis: A comprehensive meta-regression analysis.Challenges in the Understanding and Treatment of Amyotrophic Lateral Sclerosis/Motor Neuron Disease.Need for palliative care for neurological diseases.Well-being in amyotrophic lateral sclerosis: a pilot experience sampling study.Mindfulness as a Protective Factor for the Burden of Caregivers of Amyotrophic Lateral Sclerosis Patients."I hate being a burden": The patient perspective on carer burden in amyotrophic lateral sclerosis.ALS: Family caregiver needs and quality of life.Who's caring for whom? Differing perspectives between seriously ill patients and their family caregivers.Experience matters: neurologists' perspectives on ALS patients' well-being.Comparison between home and hospital as the place of death for individuals with amyotrophic lateral sclerosis in the last stages of illness.Aggressiveness, sexuality, and obsessiveness in late stages of ALS patients and their effects on caregivers.Predictors of quality of life in carers for people with a progressive neurological illness: a longitudinal study.Cross-cultural adaptation and validation of als Functional Rating Scale-Revised in Portuguese language.Discussing edaravone with the ALS patient: an ethical framework from a U.S. perspective.Eye-tracking-based assessment suggests preserved well-being in locked-in patients.Translation and Psychometric Evaluation of a Korean Version of the Amyotrophic Lateral Sclerosis-Specific Quality of Life - Revised.Supporting wellbeing in motor neurone disease for patients, carers, social networks, and health professionals: A scoping review and synthesis.
P2860
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P2860
A study comparing patients with amyotrophic lateral sclerosis and their caregivers on measures of quality of life, depression, and their attitudes toward treatment options.
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
2003年论文
@zh
2003年论文
@zh-cn
name
A study comparing patients wit ...... udes toward treatment options.
@en
type
label
A study comparing patients wit ...... udes toward treatment options.
@en
prefLabel
A study comparing patients wit ...... udes toward treatment options.
@en
P2093
P1476
A study comparing patients wit ...... udes toward treatment options.
@en
P2093
Eugene C Lai
John N Van
Marilyn Trail
Naomi D Nelson
P356
10.1016/S0022-510X(03)00003-0
P577
2003-05-01T00:00:00Z