Skeletal and Respiratory Muscle Dysfunctions in Pulmonary Arterial Hypertension

Skeletal and Respiratory Muscle Dysfunctions in Pulmonary Arterial Hypertension

Pulmonary arterial hypertension (PAH) is a rare disease, which leads to the progressive loss and remodeling of the pulmonary vessels, right heart failure, and death. Different clinical presentations can be responsible for such a bad prognosis disease and the underlying mechanisms still need to be fu...

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Bibliographic Details
Main Authors: Marianne Riou, Mégane Pizzimenti, Irina Enache, Anne Charloux, Mathieu Canuet, Emmanuel Andres, Samy Talha, Alain Meyer, Bernard Geny
Format: Article
Language:English
Published: MDPI AG 2020-02-01
Series:Journal of Clinical Medicine
Subjects:
pulmonary arterial hypertension
skeletal muscles
respiratory muscles
oxygen supply
catabolism
mitochondria
exercise
Online Access:https://www.mdpi.com/2077-0383/9/2/410

Internet

https://www.mdpi.com/2077-0383/9/2/410

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