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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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Bibliografiska uppgifter
I publikationen:Pediatr Pulmonol
Huvudupphovsmän: Beghetti, Maurice, Gorenflo, Matthias, Ivy, D. Dunbar, Moledina, Shahin, Bonnet, Damien
Materialtyp: Artigo
Språk:Inglês
Publicerad: John Wiley and Sons Inc. 2019
Ämnen:
Länkar: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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