Digitum: Repositorio Institucional de la Universidad de Murcia: Buscando en Digitum

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Vista previa	Fecha de publicación	Fecha de Creación	Título
	2012	-	Protective role of antithrombin in mouse models of liver injury
	2012	-	Congenital disorder of glycosylation (PMM2-CDG) in a patient with antithrombin deficiency and severe thrombophilia
	2012	-	Amelioration of the severity of heparin-binding antithrombin mutations by posttranslational mosaicism
	2013	-	GPI-anchor and GPI-anchored protein expression in PMM2-CDG patients
	2013	-	Identification of Antithrombin-Modulating Genes. Role of LARGE, a Gene Encoding a Bifunctional Glycosyltransferase, in the Secretion of Proteins?
	2016	-	Hypoglycosylation is a common finding in antithrombin deficiency in the absence of a SERPINC1 gene defect
	2017	-	High levels of latent antithrombin in plasma from patients with antithrombin deficiency
	2019	-	Archeogenetics of F11 p.Cys38Arg: a 5400-year-old mutation identified in different southwestern European countries
	2019	-	A human antithrombin isoform dampens inflammatory responses and protects from organ damage during bacterial infection
	2019	-	MPI-CDG with transient hypoglycosylation and antithrombin deficiency
	2019	-	International clinical guidelines for the management of phosphomannomutase 2-congenital disorders of glycosylation: Diagnosis, treatment and follow up
	2021	-	Antithrombin p.Thr147Ala: The First Founder Mutation in People of African Origin Responsible for Inherited Antithrombin Deficiency

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