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...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ferrata Storti Foundation 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5865418/
https://www.ncbi.nlm.nih.gov/pubmed/29305416
http://dx.doi.org/10.3324/haematol.2017.177816

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5865418/
https://www.ncbi.nlm.nih.gov/pubmed/29305416
http://dx.doi.org/10.3324/haematol.2017.177816

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