The progression of Duchenne muscular dystrophy is expected to negatively influence the patients' health-related quality of life, but knowledge of the relationship with disease severity is limited. We investigated the relationship between health-related quality of life (KIDSCREEN-52 questionnaire) and disease severity (clinical assessments of body functions and activities) in 40 boys with Duchenne muscular dystrophy (19 ambulant, 21 wheelchair dependent) who were in different phases of the disease and underwent life-limiting events such as the loss of the ability to ambulate and the ability to lift the arms. In addition, we compared boys' health-related quality of life perceptions with that of their parents. The participants' health-related ...
Objective: Duchenne Muscular Dystrophy (DMD) is the most severe form among a variety of muscular dys...
This cross-sectional study examined the influence that age/disease severity, pain, and/or family fun...
Participation and quality of life in children with Duchenne muscular dystrophy using the cohort of b...
Item does not contain fulltextThe progression of Duchenne muscular dystrophy is expected to negative...
Background: Duchenne muscular dystrophy is associated with variable physical and psychosocial sequal...
Muscular dystrophy is a serious congenital disease that is currently incurable. There are many types...
This study aims to assess the family functioning and health-related quality of life (HRQOL) in Chine...
Knowledge of health related quality of life (HRQOL) in the immediate phase following DMD diagnosis h...
Knowledge of health related quality of life (HRQOL) in the immediate phase following DMD diagnosis h...
We conducted a study to evaluate the quality of life in boys with Duchenne muscular dystrophy aged 8...
AIM: This study investigated the relationship between quality of life (QoL) and health-related quali...
Abstract Background Muscular dystrophies are chronic diseases manifesting with progressive muscle we...
Abstract Background This study examined the impact of Duchenne muscular dystrophy (DMD) on family-me...
This study investigated agreement between boys and their parents when reporting on health-related qu...
Objective The relationship between functional dependence and quality of life (QO...
Objective: Duchenne Muscular Dystrophy (DMD) is the most severe form among a variety of muscular dys...
This cross-sectional study examined the influence that age/disease severity, pain, and/or family fun...
Participation and quality of life in children with Duchenne muscular dystrophy using the cohort of b...
Item does not contain fulltextThe progression of Duchenne muscular dystrophy is expected to negative...
Background: Duchenne muscular dystrophy is associated with variable physical and psychosocial sequal...
Muscular dystrophy is a serious congenital disease that is currently incurable. There are many types...
This study aims to assess the family functioning and health-related quality of life (HRQOL) in Chine...
Knowledge of health related quality of life (HRQOL) in the immediate phase following DMD diagnosis h...
Knowledge of health related quality of life (HRQOL) in the immediate phase following DMD diagnosis h...
We conducted a study to evaluate the quality of life in boys with Duchenne muscular dystrophy aged 8...
AIM: This study investigated the relationship between quality of life (QoL) and health-related quali...
Abstract Background Muscular dystrophies are chronic diseases manifesting with progressive muscle we...
Abstract Background This study examined the impact of Duchenne muscular dystrophy (DMD) on family-me...
This study investigated agreement between boys and their parents when reporting on health-related qu...
Objective The relationship between functional dependence and quality of life (QO...
Objective: Duchenne Muscular Dystrophy (DMD) is the most severe form among a variety of muscular dys...
This cross-sectional study examined the influence that age/disease severity, pain, and/or family fun...
Participation and quality of life in children with Duchenne muscular dystrophy using the cohort of b...