Symptoms of anxiety and depression in patients with amyotrophic lateral sclerosis and their relatives during the disease trajectory

Informal Caregivers in Amyotrophic Lateral Sclerosis: A Multi-Centre, Exploratory Study of Burden and Difficulties

(2021) Éilís Conroy et al.   Brain Sciences

Informal Caregiving in Amyotrophic Lateral Sclerosis (ALS): A High Caregiver Burden and Drastic Consequences on Caregivers’ Lives

(2021) Pavel Schischlevskij et al.   Brain Sciences

Fatigue and anxiety mediate the effect of dyspnea on quality of life in amyotrophic lateral sclerosis

(2021) Carolyn Young et al.   Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Grief, depression, and anxiety in bereaved caregivers of people with motor neurone disease: a population-based national study

(2020) Samar M Aoun et al.   Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Individual quality of life in spousal ALS patient-caregiver dyads

(2020) Miriam Galvin et al.   Health and Quality of Life Outcomes

Psychological distress and coping styles of caregivers of patients with amyotrophic lateral sclerosis: a longitudinal study

(2019) Jessica de Wit et al.   Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

The relationships between symptoms, disability, perceived health and quality of life in amyotrophic lateral sclerosis/motor neuron disease

(2019) Carolyn Anne Young et al.   Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Do pain, anxiety and depression influence quality of life for people with amyotrophic lateral sclerosis/motor neuron disease? A national study reconciling previous conflicting literature

(2019) Rhiannon Edge et al.   JOURNAL OF NEUROLOGY

Psychological distress in partners of patients with amyotrophic lateral sclerosis and progressive muscular atrophy: what’s the role of care demands and perceived control?

(2019) Jessica de Wit et al.   Psychology Health & Medicine

Longitudinal predictors of caregiver burden in amyotrophic lateral sclerosis: a population-based cohort of patient–caregiver dyads

(2018) Tom Burke et al.   JOURNAL OF NEUROLOGY

Needs of informal caregivers across the caregiving course in amyotrophic lateral sclerosis: a qualitative analysis

(2018) Miriam Galvin et al.   BMJ Open

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

(2016) Miriam Galvin et al.   BMC Palliative Care

Interaction of physical function, quality of life and depression in Amyotrophic lateral sclerosis: characterization of a large patient cohort

(2015) Sonja Körner et al.   BMC Neurology

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

Depression and anxiety in amyotrophic lateral sclerosis: Correlations between the distress of patients and caregivers

(2015) Dezhi Chen et al.   MUSCLE & NERVE

Coping strategies among patients with newly diagnosed amyotrophic lateral sclerosis

(2014) Birgitta Jakobsson Larsson et al.   JOURNAL OF CLINICAL NURSING

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

Psychological health in patients with ALS is maintained as physical function declines

(2011) Julia Cupp et al.   Amyotrophic Lateral Sclerosis

Prevalence of major depression in ALS: Comparison of a semi-structured interview and four self-report measures

(2011) Panagiotis Ferentinos et al.   Amyotrophic Lateral Sclerosis

Measuring Symptom Distress in Palliative Care: Psychometric Properties of the Symptom Assessment Scale (SAS)

(2011) Samar M. Aoun et al.   JOURNAL OF PALLIATIVE MEDICINE

Measuring life quality, physical function and psychological well-being in neurological illness

(2010) Lorna Jane O'Doherty et al.   Amyotrophic Lateral Sclerosis

Prevalence of depression in amyotrophic lateral sclerosis and other motor disorders

(2010) L. Taylor et al.   EUROPEAN JOURNAL OF NEUROLOGY

Quality of life, anxiety and depression in ALS patients and their next of kin

(2010) Anneli G Olsson Ozanne 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

Prognostic factors in ALS: A critical review

(2009) Adriano Chiò et al.   Amyotrophic Lateral Sclerosis

Amyotrophic lateral sclerosis

(2009) Lokesh C Wijesekera et al.   Orphanet Journal of Rare Diseases

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

(2008) Virginia Murphy et al.   Amyotrophic Lateral Sclerosis

Anxiety undermines quality of life in ALS patients and caregivers

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