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

Religiousness is positively associated with quality of life of ALS caregivers

(2011) Andrea Calvo et al.   Amyotrophic Lateral Sclerosis

From symptom onset to a diagnosis of amyotrophic lateral sclerosis/motor neuron disease (ALS/MND): Experiences of people with ALS/MND and family carers – a qualitative study

(2011) Mary R. O'Brien et al.   Amyotrophic Lateral Sclerosis

The Preferred Priorities for Care document in Motor Neurone Disease: Views of bereaved relatives and carers

(2011) Harriet Preston et al.   PALLIATIVE MEDICINE

Social services homecare for people with motor neurone disease/amyotrophic lateral sclerosis: Why are such services used or refused?

(2011) Mary R O’Brien et al.   PALLIATIVE MEDICINE

Motor Neurone Disease family carers’ experiences of caring, palliative care and bereavement: An exploratory qualitative study

(2011) Samar M Aoun et al.   PALLIATIVE MEDICINE

Some difficult decisions in ALS/MND

(2010) David J. Oliver et al.   Amyotrophic Lateral Sclerosis

Cognitive and behavioral challenges in caring for patients with frontotemporal dementia and amyotrophic lateral sclerosis

(2010) Jennifer Merrilees 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

Health-related quality of life among community-dwelling patients with intractable neurological diseases and their caregivers in Japan

(2010) Mitsunori Miyashita et al.   PSYCHIATRY AND CLINICAL NEUROSCIENCES

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

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

Which carers of family members at the end of life need more support from health services and why?

(2010) Beverley McNamara et al.   SOCIAL SCIENCE & MEDICINE

Marital relationships in amyotrophic lateral sclerosis

(2009) Louise Atkins et al.   Amyotrophic Lateral Sclerosis

How common is depression among ALS caregivers? A longitudinal study

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

Socioeconomic burden of amyotrophic lateral sclerosis, myasthenia gravis and facioscapulohumeral muscular dystrophy

(2009) Karsten Schepelmann et al.   JOURNAL OF NEUROLOGY

Supporting lay carers in end of life care: current gaps and future priorities

(2009) G Grande et al.   PALLIATIVE MEDICINE

Problem solving skills predict quality of life and psychological morbidity in ALS caregivers

(2008) Virginia Murphy et al.   Amyotrophic Lateral Sclerosis

Mononeuropathy multiplex as a result of treatment with interferon-α and ribavirin in a patient with hepatitis C

(2008) C. Jacobi et al.   EUROPEAN JOURNAL OF NEUROLOGY

Anxiety undermines quality of life in ALS patients and caregivers

(2008) A. Vignola et al.   EUROPEAN JOURNAL OF NEUROLOGY

Care burden and depression in caregivers caring for patients with intractable neurological diseases at home in Japan

(2008) Mitsunori Miyashita et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Satisfaction with services among people with progressive neurological illnesses and their carers in Australia

(2008) Marita P. McCabe et al.   Nursing & Health Sciences

Quality of Life in Amyotrophic Lateral Sclerosis

(2008) Mark B. Bromberg   Physical Medicine and Rehabilitation Clinics of North America

Diagnosis and management of motor neurone disease

(2008) Christopher J McDermott et al.   BMJ-British Medical Journal