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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Haematologica
Egile Nagusiak: Lefebvre, Thibaud, Reihani, Niloofar, Daher, Raed, de Villemeur, Thierry Billette, Belmatoug, Nadia, Rose, Christian, Colin-Aronovicz, Yves, Puy, Hervé, Le Van Kim, Caroline, Franco, Mélanie, Karim, Zoubida
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Ferrata Storti Foundation 2018
Gaiak:
Article
Sarrera elektronikoa: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
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