A specific serum lipid signature characterizes patients with glycogen storage disease type Ia

Glycogen storage disease type Ia (GSDIa) is a rare, inherited glucose-6-phosphatase-α (G6Pase-α) deficiency-induced carbohydrate metabolism disorder. Although hyperlipidemia is a hallmark of GSDI, the extent of lipid metabolism disruption remains incompletely understood. Lipidomic analysis was perfo...

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Detalhes bibliográficos

Principais autores:	Alessandro Rossi, Margherita Ruoppolo, Roberta Fedele, Francesca Pirozzi, Carmen Rosano, Renata Auricchio, Daniela Melis, Pietro Strisciuglio, Maaike H. Oosterveer, Terry G.J. Derks, Giancarlo Parenti, Marianna Caterino
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Elsevier 2024-10-01
coleção:	Journal of Lipid Research
Assuntos:	hyperlipidemia serum lipidome ceramides bile acids lysophosphatidylcholine
Acesso em linha:	http://www.sciencedirect.com/science/article/pii/S0022227524001561
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