Clinical implications of maximal respiratory pressure determinations for individuals with duchenne muscular dystrophy
- 1 January 1997
- journal article
- Published by Elsevier in Archives of Physical Medicine and Rehabilitation
- Vol. 78 (1) , 1-6
- https://doi.org/10.1016/s0003-9993(97)90001-0
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- Hereditary Motor and Sensory Neuropathy, Types I and IIAmerican Journal of Physical Medicine & Rehabilitation, 1995
- Duchenne Muscular DystrophyAmerican Journal of Physical Medicine & Rehabilitation, 1995
- Spinal Muscular AtrophyAmerican Journal of Physical Medicine & Rehabilitation, 1995
- Becker??s Muscular DystrophyAmerican Journal of Physical Medicine & Rehabilitation, 1995
- Facioscapulohumeral Muscular DystrophyAmerican Journal of Physical Medicine & Rehabilitation, 1995
- Myotonic DystrophyAmerican Journal of Physical Medicine & Rehabilitation, 1995
- Evaluation of phrenic nerve and pulmonary function in hereditary motor and sensory neuropathy, type IMuscle & Nerve, 1992
- Respiratory failure and sleep in neuromuscular disease.Thorax, 1990
- Practical Problems in the Respiratory Care of Patients with Muscular DystrophyNew England Journal of Medicine, 1987
- Analysis of lung volume restriction in patients with respiratory muscle weakness.Thorax, 1980