Congenital Plasminogen Deficiency Latest Advances
Find the Latest Research About Congenital Plasminogen Deficiency
Last Updated: 06/30/2026
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Found 287 publications
Alpha-2 antiplasmin deficiency: a rare fibrinolytic disorder identified after decades of diagnostic delay.
Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
Published: June 08, 2026
Plain language summary: a phase 2/3 study of plasminogen, human-tvmh for the treatment of children and adults with type 1 plasminogen deficiency.
Journal: Expert review of hematology
Published: June 02, 2026
Cystathionine γ-lyase deficiency exacerbates high-fat diet-induced kidney and liver injury associated with disrupted glutathione homeostasis.
Journal: Free radical biology & medicine
Published: April 08, 2026
Compound heterozygous plasminogen mutations causing hereditary plasminogen deficiency: a family study and mechanistic analysis
Journal: Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi
Published: February 09, 2026
Urokinase Plasminogen Activator Deficiency Delays the Development of Obesity and Metabolic Sequelae.
Urokinase Plasminogen Activator Deficiency Delays the Development of Obesity and Metabolic Sequelae.
Journal: Arteriosclerosis, thrombosis, and vascular biology
Published: January 22, 2026
Genotype-Phenotype Correlation of Hereditary Plasminogen Deficiency: Molecular Mechanisms From 18 Patients With Cerebral Infarction.
Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: October 25, 2025
Human plasma-derived plasminogen replacement in type 1 plasminogen deficiency: a pediatric case with multisystemic manifestation.
Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
Published: September 07, 2025
Fresh frozen plasma therapy in type I plasminogen deficiency: a case of ligneous conjunctivitis with hydrocephalus.
Journal: Oxford medical case reports
Published: August 24, 2025
Lung Involvement in a Child With Type 1 Plasminogen Deficiency.
Journal: Pediatric pulmonology
Published: June 27, 2025
Novel compound heterozygous mutations in plasminogen (p.Gly568Arg/p.Ala620Thr) impair protein structure and function in type II deficiency: mechanistic insights into a hereditary thrombogenic disorder.
Journal: Orphanet journal of rare diseases
Published: June 26, 2025
Plasminogen deficiency reduces disease severity and immune responses in enterovirus A71-infected mice.
Journal: Microbiology spectrum
Published: May 16, 2025
Last Updated: 06/30/2026