טוען...
Involvement of hepcidin in iron metabolism dysregulation in Gaucher disease
Gaucher disease (GD) is an inherited deficiency of glucocerebrosidase leading to accumulation of glucosylceramide in tissues such as the spleen, liver, and bone marrow. The resulting lipid-laden macrophages lead to the appearance of “Gaucher cells”. Anemia associated with an unexplained hyperferriti...
שמור ב:
| הוצא לאור ב: | Haematologica |
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| Main Authors: | , , , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Ferrata Storti Foundation
2018
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5865418/ https://ncbi.nlm.nih.gov/pubmed/29305416 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3324/haematol.2017.177816 |
| תגים: |
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