Inspiratory pressure‐generating capacity is preserved during ventilatory and non‐ventilatory behaviours in young dystrophic mdx mice despite profound diaphragm muscle weakness
Author:
Affiliation:
1. Department of PhysiologySchool of MedicineCollege of Medicine and HealthUniversity College Cork Cork Ireland
Funder
University College Cork
Publisher
Wiley
Subject
Physiology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1113/JP277443
Reference55 articles.
1. Sleep-related respiratory disturbances in patients with Duchenne muscular dystrophy
2. Diaphragmatic function in advanced Duchenne muscular dystrophy
3. Tempol Supplementation Restores Diaphragm Force and Metabolic Enzyme Activities in mdx Mice
4. Recovery of respiratory function in mdx mice co-treated with neutralizing interleukin-6 receptor antibodies and urocortin-2
5. Evidence of hypoxic tolerance in weak upper airway muscle from young mdx mice
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