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Disease-specific platelet signaling defects in idiopathic pulmonary arterial hypertension
Idiopathic pulmonary arterial hypertension (IPAH) is a rapidly progressive disease with several treatment options. Long-term mortality remains high with great heterogeneity in treatment response. Even though most of the pathology of IPAH is observed in the lung, there is systemic involvement. Platel...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Am J Physiol Lung Cell Mol Physiol |
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| Κύριοι συγγραφείς: | , , , , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
American Physiological Society
2021
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8174825/ https://ncbi.nlm.nih.gov/pubmed/33596129 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajplung.00500.2020 |
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