A systematic review of quality of life in adults with muscle disease.
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Patient-identified disease burden in facioscapulohumeral muscular dystrophy.Do Psychosocial Interventions Improve Quality of Life and Wellbeing in Adults with Neuromuscular Disorders? A Systematic Review and Narrative Synthesis.Stability and relative validity of the Neuromuscular Disease Impact Profile (NMDIP)Health-Related Quality of Life (HRQoL) in Idiopathic Inflammatory Myopathy: A Systematic ReviewQuality of life in rehabilitation outpatients: normal values and a comparison with the general Dutch population and psychiatric patientsThe relationship between physical symptoms and health-related quality of life in oculopharyngeal muscular dystrophy.Activity rating scales in adult muscle disease: what do they actually measure?Activity rating scales in adult muscle disease: how well do they actually measure?The potential of psychological interventions to improve quality of life and mood in muscle disorders.A multicentre postal survey investigating the contribution of illness perceptions, coping and optimism to quality of life and mood in adults with muscle disease.Effectiveness of teleassistance at improving quality of life in people with neuromuscular diseases.Pain location and intensity impacts function in persons with myotonic dystrophy type 1 and facioscapulohumeral dystrophy with chronic pain.A method for assessing heterogeneity of blood flow and metabolism in exercising normal human muscle by near-infrared spectroscopy.The use of an online support group for neuromuscular disorders: a thematic analysis of message postings.The individualized neuromuscular quality of life questionnaire: cultural translation and psychometric validation for the Dutch population.Correlates of health related quality of life in adult patients with spinal muscular atrophy.What Matters Most: A Perspective From Adult Spinal Muscular Atrophy Patients.Suite of clinically relevant functional assays to address therapeutic efficacy and disease mechanism in the dystrophic mdx mouse.Health-related quality of life and well-being in adults with idiopathic inflammatory myopathy.Exercise prevents impaired autophagy and proteostasis in a model of neurogenic myopathyA Review of Psychopathology Features, Personality, and Coping in Myotonic Dystrophy Type 1
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P2860
A systematic review of quality of life in adults with muscle disease.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 20 May 2011
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
A systematic review of quality of life in adults with muscle disease.
@en
A systematic review of quality of life in adults with muscle disease.
@en-gb
A systematic review of quality of life in adults with muscle disease.
@nl
type
label
A systematic review of quality of life in adults with muscle disease.
@en
A systematic review of quality of life in adults with muscle disease.
@en-gb
A systematic review of quality of life in adults with muscle disease.
@nl
prefLabel
A systematic review of quality of life in adults with muscle disease.
@en
A systematic review of quality of life in adults with muscle disease.
@en-gb
A systematic review of quality of life in adults with muscle disease.
@nl
P2860
P50
P1433
P1476
A systematic review of quality of life in adults with muscle disease.
@en
P2093
Michael R Rose
P2860
P2888
P304
P356
10.1007/S00415-011-6062-5
P577
2011-05-20T00:00:00Z