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Targeting novel mechanisms of pain in sickle cell disease
Patients with sickle cell disease (SCD) suffer from intense pain that can start during infancy and increase in severity throughout life, leading to hospitalization and poor quality of life. A unique feature of SCD is vaso-occlusive crises (VOCs) characterized by episodic, recurrent, and unpredictabl...
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| Yayımlandı: | Blood |
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| Asıl Yazarlar: | , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
American Society of Hematology
2017
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5709786/ https://ncbi.nlm.nih.gov/pubmed/29187376 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2017-05-782003 |
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