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Roesel RA, Hommes FA, Samper L: Pyroglutamic aciduria (5-oxoprolinuria) without glutathione synthetase deficiency and with decreased pyroglutamate hydrolase activity

In patients with neurological manifestations, prompt treatment can halt progression and potentially reverse symptoms

[DOI] [PubMed] [Google Scholar] 75.Zhao W, Zhang J, Lu Y, Wang R

Pour la protger, une des solutions est de lentourer de lipides (liposomes) afin de favoriser lassimilation intestinale : cest ce que lon appelle la microencapsulation

Due to its amphiphilic structure, ALA is soluble in both aqueous and lipidic environments

Identifying novel therapeutic targets in cystic fibrosis through advanced single-cell transcriptomics analysis