| scholarly article | Q13442814 |
| P50 | author | Adriano Chiò | Q30003371 |
| P2093 | author name string | Gauthier A | |
| Mutani R | |||
| Calvo A | |||
| Di Vito N | |||
| Ghiglione P | |||
| Montuschi A | |||
| P2860 | cites work | “Mini-mental state” | Q25938989 |
| A SELF-RATING DEPRESSION SCALE | Q28201088 | ||
| Pathological laughing and crying following stroke: validation of a measurement scale and a double-blind treatment study | Q28265388 | ||
| Improving the quality of life for people with ALS: the challenge ahead | Q34314315 | ||
| The McGill Quality of Life Questionnaire: a measure of quality of life appropriate for people with advanced disease. A preliminary study of validity and acceptability | Q34720132 | ||
| A new short form individual quality of life measure (SEIQoL-DW): application in a cohort of individuals with HIV/AIDS. | Q36599136 | ||
| Resilience and distress among amyotrophic lateral sclerosis patients and caregivers | Q39263471 | ||
| Predictors and correlates of interest in assisted suicide in the final month of life among ALS patients in Oregon and Washington | Q40618574 | ||
| Attitudes of patients with amyotrophic lateral sclerosis and their care givers toward assisted suicide | Q40841753 | ||
| Amyotrophic lateral sclerosis and hopelessness: psychosocial factors | Q47345206 | ||
| Correlates of suffering in amyotrophic lateral sclerosis | Q47348801 | ||
| The measurement of pessimism: the hopelessness scale. | Q47359395 | ||
| Euthanasia and physician-assisted suicide among patients with amyotrophic lateral sclerosis in the Netherlands. | Q51716340 | ||
| Agreement among three quality of life measures in patients with ALS. | Q51965056 | ||
| Spiritual well-being of the individual with amyotrophic lateral sclerosis. | Q51965068 | ||
| Impact of spirituality and religiousness on outcomes in patients with ALS. | Q51971913 | ||
| Validity of the McGill Quality of Life Questionnaire in the palliative care setting: a multi-centre Canadian study demonstrating the importance of the existential domain. | Q52005191 | ||
| Survival in amyotrophic lateral sclerosis. The role of psychological factors. | Q52029503 | ||
| The functional and psychological status of patients with amyotrophic lateral sclerosis: some implications for rehabilitation. | Q52034829 | ||
| Patients' assessment of quality of life instruments: a randomised study of SIP, SF-36 and SEIQoL-DW in patients with amyotrophic lateral sclerosis. | Q52128193 | ||
| A neuropsychological investigation of dementia in motor neurone disease (MND). | Q52144471 | ||
| Religiousness is related to quality of life in patients with ALS | Q52951184 | ||
| Fatigue and depression are associated with poor quality of life in ALS. | Q53400703 | ||
| Correlates of Quality of Life in people with motor neuron disease (MND). | Q53402921 | ||
| Assessing individual quality of life in amyotrophic lateral sclerosis. | Q53468566 | ||
| Quality of life in ALS depends on factors other than strength and physical function. | Q53515661 | ||
| Quality of life assessment in MND: development of a social withdrawal scale. | Q53535981 | ||
| Against all odds: positive life experiences of people with advanced amyotrophic lateral sclerosis. | Q53581382 | ||
| The psychological impact of motor neurone disease. | Q53659518 | ||
| Patients' health-related quality of life and utilities associated with different stages of amyotrophic lateral sclerosis | Q57942823 | ||
| Evidence for the validity and reliability of the ALS assessment questionnaire: The ALSAQ-40 | Q58271831 | ||
| Quality of life in ALS is maintained as physical function declines | Q73550691 | ||
| P433 | issue | 11 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | amyotrophic lateral sclerosis | Q206901 |
| quality of life | Q13100823 | ||
| P304 | page(s) | 1597-1601 | |
| P577 | publication date | 2004-11-01 | |
| P1433 | published in | Journal of Neurology, Neurosurgery and Psychiatry | Q1599804 |
| P1476 | title | A cross sectional study on determinants of quality of life in ALS. | |
| P478 | volume | 75 |
| Q26775401 | A comprehensive review of amyotrophic lateral sclerosis |
| Q38775462 | A prospective study of quality of life in amyotrophic lateral sclerosis patients |
| Q40073457 | ALS: Family caregiver needs and quality of life |
| Q47692052 | Apathy and its impact on patient outcome in amyotrophic lateral sclerosis |
| Q37333922 | Assessing social isolation in motor neurone disease: a Rasch analysis of the MND Social Withdrawal Scale |
| Q36075065 | Assessment of disease progression in motor neuron disease |
| Q26738679 | Associations between psychological factors and health-related quality of life and global quality of life in patients with ALS: a systematic review |
| Q92637315 | Associations of Patient Mood, Modulators of Quality of Life, and Pharmaceuticals with Amyotrophic Lateral Sclerosis Survival Duration |
| Q48947706 | Burden, depression, and anxiety in caregivers of people with amyotrophic lateral sclerosis |
| Q47978176 | Caregiver burden in amyotrophic lateral sclerosis: a cross-sectional investigation of predictors |
| Q35157186 | Clinical psychology and amyotrophic lateral sclerosis. |
| Q46101846 | Cognitive-behavioral changes in amyotrophic lateral sclerosis: Screening prevalence and impact on patients and caregivers |
| Q30365902 | Comprehensive rehabilitative care across the spectrum of amyotrophic lateral sclerosis. |
| Q33864113 | Coping strategies as related to medical and demographic data in amyotrophic lateral sclerosis |
| Q48513607 | Coping strategies in relation to quality of life in amyotrophic lateral sclerosis |
| Q87381284 | Correlations in health status between estimates of families of people with amyotrophic lateral sclerosis and estimates of staff |
| Q50881104 | Cross-sectional and longitudinal correlations between disease progression and different health-related quality of life domains in persons with amyotrophic lateral sclerosis. |
| Q47854725 | Depression and anxiety in amyotrophic lateral sclerosis: correlations between the distress of patients and caregivers |
| Q36768040 | Depression and anxiety in individuals with amyotrophic lateral sclerosis: epidemiology and management |
| Q38207001 | Depression and disease progression in amyotrophic lateral sclerosis: A comprehensive meta-regression analysis. |
| Q80092070 | Depression and quality of life issues in patients with amyotrophic lateral sclerosis |
| Q35163766 | Depression in amyotrophic lateral sclerosis |
| Q37267129 | Depression, pain and quality of life in patients with amyotrophic lateral sclerosis: a cross-sectional study |
| Q48882658 | Differences in quality of life modalities give rise to needs of individual support in patients with ALS and their next of kin. |
| Q48658828 | Disease severity affects quality of life of hereditary spastic paraplegia patients. |
| Q47792393 | Effect of a short-term psychological intervention on the anxiety and depression of amyotrophic lateral sclerosis patients |
| Q64061203 | Ethical Principles in Patient-Centered Medical Care to Support Quality of Life in Amyotrophic Lateral Sclerosis |
| Q58657043 | Ethical challenges in tracheostomy-assisted ventilation in amyotrophic lateral sclerosis |
| Q26748130 | Evaluation of quality of life in individuals with severe chronic motor disability: A major challenge |
| Q48569701 | Experience of services as a key outcome in amyotrophic lateral sclerosis (ALS) care: the case for a better understanding of patient experiences |
| Q39274996 | 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 |
| Q91938042 | Exploring and Addressing 'Concerns' for Significant Others to Extend the Understanding of Quality of Life With Amyotrophic Lateral Sclerosis: A Qualitative Study |
| Q47592064 | Eye-tracking-based assessment suggests preserved well-being in locked-in patients. |
| Q90202873 | Group interventions for amyotrophic lateral sclerosis caregivers in Ireland: a randomised controlled trial protocol |
| Q47728396 | Health Status Perspectives in Amyotrophic Lateral Sclerosis |
| Q44219897 | Health utility decreases with increasing clinical stage in amyotrophic lateral sclerosis |
| Q48747132 | Health-related quality of life among community-dwelling patients with intractable neurological diseases and their caregivers in Japan |
| Q44545095 | Health-related quality of life in ALS, myasthenia gravis and facioscapulohumeral muscular dystrophy |
| Q35538809 | Home-based palliative approach for people with severe multiple sclerosis and their carers: study protocol for a randomized controlled trial |
| Q35749276 | Hypnosis-based psychodynamic treatment in ALS: a longitudinal study on patients and their caregivers. |
| Q35367839 | Identification of personal factors in motor neurone disease: a pilot study |
| Q48056893 | Individualized quality of life of severely affected multiple sclerosis patients: practicability and value in comparison with standard inventories |
| Q30656923 | Interaction of physical function, quality of life and depression in Amyotrophic lateral sclerosis: characterization of a large patient cohort |
| Q48112130 | Longitudinal predictors of caregiver burden in amyotrophic lateral sclerosis: a population-based cohort of patient-caregiver dyads |
| Q48873738 | Measuring life quality, physical function and psychological well-being in neurological illness |
| Q45286756 | Modafinil to treat fatigue in amyotrophic lateral sclerosis: an open label pilot study |
| Q48830872 | Neurobehavioral symptoms in ALS are negatively related to caregivers' burden and quality of life. |
| Q55223612 | Neurological Symptoms in Palliative Care Patients. |
| Q37212835 | Patient and caregiver quality of life in Huntington's disease |
| Q53190192 | Perceptions of quality of life in people with ALS: effects of coping and health care. |
| Q45034684 | Prevalence of depression in amyotrophic lateral sclerosis and other motor disorders |
| Q49438915 | Progression and effect of cognitive-behavioral changes in patients with amyotrophic lateral sclerosis |
| Q44495627 | Psychiatric aspects of amyotrophic lateral sclerosis (ALS). |
| Q36892310 | Psychological health in patients with amyotrophic lateral sclerosis |
| Q38021491 | Psychological wellbeing and quality of life in amyotrophic lateral sclerosis: a review |
| Q51850217 | Psychopathological features and suicidal ideation in amyotrophic lateral sclerosis patients. |
| Q36056010 | Psychosocial adjustment to ALS: a longitudinal study |
| Q51102541 | Purposes of AAC device use for persons with ALS as reported by caregivers. |
| Q41066718 | Pyrimethamine significantly lowers cerebrospinal fluid Cu/Zn superoxide dismutase in amyotrophic lateral sclerosis patients with SOD1 mutations |
| Q34616055 | Quality of life and motor impairment in ALS: Italian validation of ALSAQ. |
| Q48044184 | Quality of life in amyotrophic lateral sclerosis patients and caregivers: Impact of assistive communication from early stages |
| Q37254391 | Quality of life in amyotrophic lateral sclerosis/motor neuron disease: a structured review |
| Q35863798 | Quality of life in patients with locked-in syndrome: Evolution over a 6-year period |
| Q50707459 | Requests for euthanasia: origin of suffering in ALS, heart failure, and cancer patients. |
| Q36517238 | Self perceived emotional functioning of spanish patients with amyotrophic lateral sclerosis: a longitudinal study |
| Q53285749 | Severity of depressive symptoms and quality of life in patients with amyotrophic lateral sclerosis. |
| Q48233453 | The impact of fatigue and psychosocial variables on quality of life for patients with motor neuron disease |
| Q37620438 | The patient experience of fatigue in motor neurone disease |
| Q86517348 | The role of palliative care in patients with neurological diseases |
| Q37507780 | The use, feasibility and psychometric properties of an individualised quality-of-life instrument: a systematic review of the SEIQoL-DW. |
| Q48361667 | The views of adults with neurodegenerative diseases on end-of-life care: a metasynthesis. |
| Q42003585 | Theory of Mind and Its Neuropsychological and Quality of Life Correlates in the Early Stages of Amyotrophic Lateral Sclerosis |
| Q47609979 | Translation and Psychometric Evaluation of a Korean Version of the Amyotrophic Lateral Sclerosis-Specific Quality of Life - Revised. |
| Q47584269 | Usability of eyetracking computer systems and impact on psychological wellbeing in patients with advanced amyotrophic lateral sclerosis |
| Q39838623 | Verbal communication impacts quality of life in patients with amyotrophic lateral sclerosis |
| Q39152252 | Well-being in amyotrophic lateral sclerosis: a pilot experience sampling study |
| Q83060899 | [Quality of life measurement: a fashion or a valid assessment?] |
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