Histomorphometric analysis of liver biopsies of treated patients with Gaucher disease type 1

Gaucher disease (GD) is an autosomal recessive lysosomal disorder caused by a disturbance in the metabolism of glucocerebroside in the macrophages. Most of its manifestations – hepatosplenomegaly, anemia, thrombocytopenia, and bone pain – are amenable to a macrophage-target therapy such as enzyme re...

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Detalles Bibliográficos
Autores principales: Starosta, Rodrigo Tzovenos, Siebert, Marina, Vairo, Filippo Pinto e, Costa, Bruno Lafaiete de Lima, Ponzoni, Christiano Tomaso, Schwartz, Ida Vanessa Doederlein, Cerski, Carlos Thadeu Schmidt
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hospital Universitário da Universidade de São Paulo 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8387085/
https://www.ncbi.nlm.nih.gov/pubmed/34458174
http://dx.doi.org/10.4322/acr.2021.306

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8387085/
https://www.ncbi.nlm.nih.gov/pubmed/34458174
http://dx.doi.org/10.4322/acr.2021.306

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