Imaging of non-neuronopathic Gaucher disease: recent advances in quantitative imaging and comprehensive assessment of disease involvement

Gaucher disease is an inherited metabolic disorder resulting in deficiency of lysosomal enzyme β-glucocerebrosidase causing the accumulation of abnormal macrophages (“Gaucher cells”) within multiple organs, most conspicuously affecting the liver, spleen, and bone marrow. As the most common glycolipi...

Descripción completa

Detalles Bibliográficos
Autores principales: Degnan, Andrew J., Ho-Fung, Victor M., Ahrens-Nicklas, Rebecca C., Barrera, Christian A., Serai, Suraj D., Wang, Dah-Jyuu, Ficicioglu, Can
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2019
Materias:
Critical Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6616606/
https://www.ncbi.nlm.nih.gov/pubmed/31289964
http://dx.doi.org/10.1186/s13244-019-0743-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6616606/
https://www.ncbi.nlm.nih.gov/pubmed/31289964
http://dx.doi.org/10.1186/s13244-019-0743-5

Ejemplares similares