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Background: Pulmonary arterial hypertension (PAH) is one of several cardiovascular complications in patients with thalassemia, and significant cause of mortality and morbidity. The etiology is multifactorial and one of the… Click to show full abstract
Background: Pulmonary arterial hypertension (PAH) is one of several cardiovascular complications in patients with thalassemia, and significant cause of mortality and morbidity. The etiology is multifactorial and one of the important mechanisms is a decrease in nitric oxide (NO) resulting in
Keywords:
nebulized nitrite;
arterial hypertension;
pulmonary arterial;
effect inhaled;
inhaled nebulized
Journal Title: Journal of the American College of Cardiology
Year Published: 2017
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Journal Title: Journal of the American College of Cardiology
Year Published: 2017
Link to full text (if available)
Share on Social Media: Sign Up to like & get
recommendations!