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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Detalhes bibliográficos
Publicado no:Syst Rev
Main Authors: Raskovalova, Tatiana, Deegan, Patrick B., Yang, Ruby, Pavlova, Elena, Stirnemann, Jérome, Labarère, José, Zimran, Ari, Mistry, Pramod K., Berger, Marc
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2017
Assuntos:
Protocol
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5397740/
https://ncbi.nlm.nih.gov/pubmed/28427477
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13643-017-0483-x
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