Psychological distress and coping styles of caregivers of patients with amyotrophic lateral sclerosis: a longitudinal study-Reference-Cited by-同舟云学术

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

Published:2019-01-18 Issue:3-4 Volume:20 Page:235-241
ISSN:2167-8421
Container-title:Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
language:en
Short-container-title:Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Author:

de Wit Jessica¹^ORCID,Bakker Leonhard A.¹²^ORCID,van Groenestijn Annerieke C.³^ORCID,Baardman Joost F.¹,van den Berg Leonard H.²^ORCID,Visser-Meily Johanna M.A.¹⁴^ORCID,SchrÖder Carin D.¹^ORCID

Affiliation:

1. Center of Excellence for Rehabilitation Medicine, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht University and De Hoogstraat Rehabilitation, Utrecht, The Netherlands;

2. Department of Neurology, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, The Netherlands;

3. Department of Rehabilitation, Amsterdam Movement Sciences, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands;

4. Department of Rehabilitation, Physical Therapy Science & Sports, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, The Netherlands

Funder

The Netherlands Organization for Health Research and Development

the Prinses Beatrix Spierfonds

Publisher

Informa UK Limited

Subject

Neurology (clinical),Neurology

Link

https://tandfonline.com/doi/pdf/10.1080/21678421.2018.1534976

Reference34 articles.

1. The family experience of living with a person with amyotrophic lateral sclerosis: A qualitative study

2. A longitudinal study on quality of life and depression in ALS patient–caregiver couples