Value of Glucosylsphingosine (Lyso-Gb1) as a Biomarker in Gaucher Disease: A Systematic Literature Review

The challenges in the diagnosis, prognosis, and monitoring of Gaucher disease (GD), an autosomal recessive inborn error of glycosphingolipid metabolism, can negatively impact clinical outcomes. This systematic literature review evaluated the value of glucosylsphingosine (lyso-Gb1), as the most relia...

Descripción completa

Detalles Bibliográficos
Autores principales: Revel-Vilk, Shoshana, Fuller, Maria, Zimran, Ari
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7584006/
https://www.ncbi.nlm.nih.gov/pubmed/32998334
http://dx.doi.org/10.3390/ijms21197159

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7584006/
https://www.ncbi.nlm.nih.gov/pubmed/32998334
http://dx.doi.org/10.3390/ijms21197159

Ejemplares similares