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Plasma receptor tyrosine kinase RET in pulmonary arterial hypertension diagnosis and differentiation
BACKGROUND: Pulmonary arterial hypertension (PAH) is a serious disease exhibiting unspecific symptoms, as a result of which diagnosis is often delayed and prognosis is poor. The underlying pathophysiology includes vasoconstriction and remodelling of small pulmonary arteries. As receptor tyrosine kin...
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| Publicado no: | ERJ Open Res |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
European Respiratory Society
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6856495/ https://ncbi.nlm.nih.gov/pubmed/31754623 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1183/23120541.00037-2019 |
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