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Paroxysmal nocturnal hemoglobinuria: When delay in diagnosis and long therapy occurs
Paroxysmal nocturnal hemoglobinuria (PNH) is a rare clonal disorder characterized by hemolytic anemia, bone marrow failure and thrombosis, caused by a somatic mutation in PIG-A gene that results in the absence of CD55 and CD59, two important complement regulatory proteins. In this paper, a case of P...
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| Publicado no: | Hematol Rep |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
PAGEPress Publications, Pavia, Italy
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5907647/ https://ncbi.nlm.nih.gov/pubmed/29721255 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4081/hr.2018.7523 |
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