Caregiver burden in amyotrophic lateral sclerosis: A systematic review

Patients’ self-perceived burden, caregivers’ burden and quality of life for amyotrophic lateral sclerosis patients: a cross-sectional study

(2017) Dan Geng et al.   JOURNAL OF CLINICAL NURSING

Are Amyotrophic Lateral Sclerosis Caregivers at Higher Risk for Health Problems?

(2016) Ana Catarina Pinho et al.   Acta Medica Portuguesa

Behavioural But Not Cognitive Impairment Is a Determinant of Caregiver Burden in Amyotrophic Lateral Sclerosis

(2016) Lucio Tremolizzo et al.   EUROPEAN NEUROLOGY

Associations between psychological factors and health-related quality of life and global quality of life in patients with ALS: a systematic review

(2016) Annerieke C. van Groenestijn et al.   Health and Quality of Life Outcomes

Which behaviours? Identifying the most common and burdensome behaviour changes in amyotrophic lateral sclerosis

(2016) Sophie Claire Andrews et al.   Psychology Health & Medicine

Cognitive-behavioral changes in amyotrophic lateral sclerosis: Screening prevalence and impact on patients and caregivers

(2016) Meredith Bock et al.   Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Caregiving in ALS – a mixed methods approach to the study of Burden

(2016) Miriam Galvin et al.   BMC Palliative Care

Caregiver burden for informal caregivers of patients with dementia: A systematic review

(2015) C.-Y. Chiao et al.   INTERNATIONAL NURSING REVIEW

Caregiver burden in amyotrophic lateral sclerosis: a cross-sectional investigation of predictors

(2015) Tom Burke et al.   JOURNAL OF NEUROLOGY

Factors related to caregiver strain in ALS: a longitudinal study

(2015) Huub Creemers et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

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

(2015) Fabia B Weisser et al.   PALLIATIVE MEDICINE

Impact of disease, cognitive and behavioural factors on caregiver outcome in amyotrophic lateral sclerosis

(2015) Tamlyn J. Watermeyer et al.   Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Multivariate models of subjective caregiver burden in dementia: A systematic review

(2014) Jacqueline van der Lee et al.   AGEING RESEARCH REVIEWS

Age, gender, kinship and caregiver burden in amyotrophic lateral sclerosis

(2014) Francesco Tramonti et al.   Psychology Health & Medicine

A permanent emergency: A longitudinal study on families coping with amyotrophic lateral sclerosis.

(2014) Francesco Tramonti et al.   Families Systems & Health

Minorities, men, and unmarried amyotrophic lateral sclerosis patients are more likely to die in an acute care facility

(2014) Stephen A. Goutman et al.   Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Life factors affecting depression and burden in amyotrophic lateral sclerosis caregivers

(2014) Kristen Qutub et al.   Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Caregiver burden in amyotrophic lateral sclerosis is more dependent on patients’ behavioral changes than physical disability: a comparative study

(2012) Patricia Lillo et al.   BMC Neurology

A 10-year literature review of family caregiving for motor neurone disease: Moving from caregiver burden studies to palliative care interventions

(2012) Samar M Aoun et al.   PALLIATIVE MEDICINE

The syndrome of cognitive impairment in amyotrophic lateral sclerosis: a population-based study

(2011) Julie Phukan et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Impact of patient suffering on caregiver well-being: The case of amyotrophic lateral sclerosis patients and their caregivers

(2011) Kathrin Boerner et al.   Psychology Health & Medicine

Associations between psychological factors and quality of life ratings in persons with spinal cord injury: a systematic review

(2011) C M C van Leeuwen et al.   SPINAL CORD

Existential well-being and spirituality of individuals with amyotrophic lateral sclerosis is related to psychological well-being of their caregivers

(2010) Francesco Pagnini et al.   Amyotrophic Lateral Sclerosis

How common are behavioural changes in amyotrophic lateral sclerosis?

(2010) Patricia Lillo et al.   Amyotrophic Lateral Sclerosis

Neurobehavioral symptoms in ALS are negatively related to caregivers’ burden and quality of life

(2010) A. Chiò et al.   EUROPEAN JOURNAL OF NEUROLOGY

Living with amyotrophic lateral sclerosis/motor neurone disease (ALS/MND): decision-making about ‘ongoing change and adaptation’

(2010) Susan J King et al.   JOURNAL OF CLINICAL NURSING

Burden, depression, and anxiety in caregivers of people with amyotrophic lateral sclerosis

(2010) Francesco Pagnini et al.   Psychology Health & Medicine

How common is depression among ALS caregivers? A longitudinal study

(2009) Judith G. Rabkin et al.   Amyotrophic Lateral Sclerosis

Consensus criteria for the diagnosis of frontotemporal cognitive and behavioural syndromes in amyotrophic lateral sclerosis

(2009) Michael J. Strong et al.   Amyotrophic Lateral Sclerosis

A Systematic Review of Caregiver Burden following Stroke

(2009) H. Rigby et al.   International Journal of Stroke

ALS: Family caregiver needs and quality of life

(2008) Mary Tederous Williams et al.   Amyotrophic Lateral Sclerosis