Quality of life, physical disability, and respiratory impairment in Duchenne muscular dystrophy. - Wikidata - awgldk - TriplyDB

Quality of life, physical disability, and respiratory impairment in Duchenne muscular dystrophy.

Quality of life, physical disability, and respiratory impairment in Duchenne muscular dystrophy.

http://www.wikidata.org/entity/Q47778864

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Interventions for increasing ankle range of motion in patients with neuromuscular disease Aminoglycosides and other nonsense suppression therapies for the treatment of dystrophinopathy Dystrophin and the two related genetic diseases, Duchenne and Becker muscular dystrophies Quality improvement in neurology: muscular dystrophy quality measures Quality of life and measures of quality of life in patients with neuromuscular disorders.Non-invasive brain-computer interface system: towards its application as assistive technology.Living with severe physical impairment, Duchenne's muscular dystrophy and home mechanical ventilation Impact of three genetic musculoskeletal diseases: a comparative synthesis of achondroplasia, Duchenne muscular dystrophy and osteogenesis imperfecta.Measuring quality of life in muscular dystrophy.Long term non-invasive ventilation in children: impact on survival and transition to adult care.Living with muscular dystrophy: health related quality of life consequences for children and adults Gastrointestinal Dysfunction in Patients with Duchenne Muscular Dystrophy Respiratory involvement in inherited primary muscle conditions.Mechanical ventilation in Duchenne patients with chronic respiratory insufficiency: clinical implications of 20 years published experience.Health-related quality of life in patients with Duchenne muscular dystrophy: a multinational, cross-sectional study.Role of beta-adrenoceptor signaling in skeletal muscle: implications for muscle wasting and disease.Rate of oral intake and effects of mechanical insufflation-exsufflation on pulmonary complications in patients with duchenne muscular dystrophy.A systematic review of quality of life in adults with muscle disease.Communication regarding breathing support options for youth with Duchenne muscular dystrophy.Reliability of home-based, motor function measure in hereditary neuromuscular diseases Patient-centered benefit-risk assessment in duchenne muscular dystrophy.Health-Related Quality of Life in Children with DuchenneMuscular Dystrophy: A Review.Functional correction in mouse models of muscular dystrophy using exon-skipping tricyclo-DNA oligomers.Dystrophin and Spectrin, Two Highly Dissimilar Sisters of the Same Family.A multicentre postal survey investigating the contribution of illness perceptions, coping and optimism to quality of life and mood in adults with muscle disease.Effects of glucocorticoids and idebenone on respiratory function in patients with duchenne muscular dystrophy.Participation and quality of life in children with Duchenne muscular dystrophy using the International Classification of Functioning, Disability, and Health Health perceptions of young adults living with recessive limb-girdle muscular dystrophy.The quality of life of home-ventilated children and their primary caregivers plus the associated social and economic burdens: a prospective study.Long-term ventilation of patients with Duchenne muscular dystrophy: experiences at the Neuromuscular Centre Ulm.Efficacy and Safety Profile of Tricyclo-DNA Antisense Oligonucleotides in Duchenne Muscular Dystrophy Mouse Model Noninvasive Respiratory Management of Patients With Neuromuscular Disease Chronic ventilation and social participation: experiences of men with neuromuscular disorders.Health-related quality of life and its relation to disease severity in boys with Duchenne muscular dystrophy: satisfied boys, worrying parents--a case-control study.Eteplirsen for the treatment of Duchenne muscular dystrophy.Correlates of health related quality of life in adult patients with spinal muscular atrophy.Is functional dependence of Duchenne muscular dystrophy patients determinant of the quality of life and burden of their caregivers?Correlates of care for young men with Duchenne and Becker muscular dystrophy.Community-based study of health-related quality of life in spinal cord injury, muscular dystrophy, multiple sclerosis, and cerebral palsy.Quality of life in Duchenne muscular dystrophy: the subjective impact on children and parents.

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P2860

Quality of life, physical disability, and respiratory impairment in Duchenne muscular dystrophy.

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2005 nî lūn-bûn

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Quality of life, physical disa ...... n Duchenne muscular dystrophy.

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Quality of life, physical disa ...... n Duchenne muscular dystrophy.

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American Journal of Respiratory and Critical Care Medicine

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Quality of life, physical disa ...... n Duchenne muscular dystrophy.

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Christian F Clarenbach

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Erich W Russi

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Konrad E Bloch

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Lukas Böni

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Thomas Brack

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P2860

Standardization of Spirometry, 1994 Update. American Thoracic Society

The heart in human dystrophinopathies.

Maximal values of sniff nasal inspiratory pressure in healthy subjects.

Practical problems in the respiratory care of patients with muscular dystrophy.

Impact of nasal ventilation on survival in hypercapnic Duchenne muscular dystrophy.

Sniff nasal inspiratory pressure. Reference values in Caucasian children.

Disability, coping and quality of life in individuals with muscular dystrophy: a prospective study over five years.

STUDIES OF ILLNESS IN THE AGED. THE INDEX OF ADL: A STANDARDIZED MEASURE OF BIOLOGICAL AND PSYCHOSOCIAL FUNCTION.

Improved quality of life after lung volume reduction surgery.

Long-term ventilation for patients with Duchenne muscular dystrophy : physicians' beliefs and practices.

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quality of life