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Treatment of pediatric pulmonary arterial hypertension: A focus on the NO‐sGC‐cGMP pathway

OBJECTIVE: While pulmonary arterial hypertension (PAH) is rare in infants and children, it results in substantial morbidity and mortality. In recent years, prognosis has improved, coinciding with the introduction of new PAH‐targeted therapies, although much of their use in children is off‐label. Evi...

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Enregistré dans:
Détails bibliographiques
Publié dans:Pediatr Pulmonol
Auteurs principaux: Beghetti, Maurice, Gorenflo, Matthias, Ivy, D. Dunbar, Moledina, Shahin, Bonnet, Damien
Format: Artigo
Langue:Inglês
Publié: John Wiley and Sons Inc. 2019
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC6771736/
https://ncbi.nlm.nih.gov/pubmed/31313530
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ppul.24442
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