Plasma chitotriosidase activity versus CCL18 level for assessing type I Gaucher disease severity: protocol for a systematic review with meta-analysis of individual participant data

BACKGROUND: Gaucher disease (GD) is an autosomal recessive lysosomal storage disorder caused by deficiency in acid beta-glucosidase. GD exhibits a wide clinical spectrum of disease severity with an unpredictable natural course. Plasma chitotriosidase activity and CC chemokine ligand 18 (CCL18) have...

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Detalles Bibliográficos
Autores principales: Raskovalova, Tatiana, Deegan, Patrick B., Yang, Ruby, Pavlova, Elena, Stirnemann, Jérome, Labarère, José, Zimran, Ari, Mistry, Pramod K., Berger, Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Protocol
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5397740/
https://www.ncbi.nlm.nih.gov/pubmed/28427477
http://dx.doi.org/10.1186/s13643-017-0483-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5397740/
https://www.ncbi.nlm.nih.gov/pubmed/28427477
http://dx.doi.org/10.1186/s13643-017-0483-x

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