Congenital Plasminogen Deficiency Latest Advances

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.

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

Congenital Holoprocencephaly, Hydrocephalus, and Dandy-Walker Malformation Due to Plasminogen Deficiency.

Journal: Cureus

Published: October 07, 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

Urokinase-type plasminogen activator deficiency enhances CD8+ T cell infiltration and anti-PD-1 therapy efficacy in prostate cancer.

Journal: Frontiers in immunology

Published: May 08, 2025

Ligneous periodontitis: A molecularly confirmed case of type I plasminogen deficiency.

Journal: Journal of clinical and experimental dentistry

Published: March 27, 2025

Perinatal Intracranial Hemorrhage as a Rare Presentation of Plasminogen Activator Inhibitor-1 (PAI-1) Deficiency: A Case Report.

Journal: Cureus

Published: March 20, 2025

Congenital Plasminogen Deficiency Latest Advances

Find the Latest Research About Congenital Plasminogen Deficiency

Compound heterozygous plasminogen mutations causing hereditary plasminogen deficiency: a family study and mechanistic analysis

Compound heterozygous plasminogen mutations causing hereditary plasminogen deficiency: a family study and mechanistic analysis

Urokinase Plasminogen Activator Deficiency Delays the Development of Obesity and Metabolic Sequelae.

Urokinase Plasminogen Activator Deficiency Delays the Development of Obesity and Metabolic Sequelae.

Genotype-Phenotype Correlation of Hereditary Plasminogen Deficiency: Molecular Mechanisms From 18 Patients With Cerebral Infarction.

Genotype-Phenotype Correlation of Hereditary Plasminogen Deficiency: Molecular Mechanisms From 18 Patients With Cerebral Infarction.

Congenital Holoprocencephaly, Hydrocephalus, and Dandy-Walker Malformation Due to Plasminogen Deficiency.

Congenital Holoprocencephaly, Hydrocephalus, and Dandy-Walker Malformation Due to Plasminogen Deficiency.

Human plasma-derived plasminogen replacement in type 1 plasminogen deficiency: a pediatric case with multisystemic manifestation.

Human plasma-derived plasminogen replacement in type 1 plasminogen deficiency: a pediatric case with multisystemic manifestation.

Fresh frozen plasma therapy in type I plasminogen deficiency: a case of ligneous conjunctivitis with hydrocephalus.

Fresh frozen plasma therapy in type I plasminogen deficiency: a case of ligneous conjunctivitis with hydrocephalus.

Lung Involvement in a Child With Type 1 Plasminogen Deficiency.

Lung Involvement in a Child With Type 1 Plasminogen Deficiency.

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.

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.

Plasminogen deficiency reduces disease severity and immune responses in enterovirus A71-infected mice.

Plasminogen deficiency reduces disease severity and immune responses in enterovirus A71-infected mice.

Urokinase-type plasminogen activator deficiency enhances CD8+ T cell infiltration and anti-PD-1 therapy efficacy in prostate cancer.

Urokinase-type plasminogen activator deficiency enhances CD8+ T cell infiltration and anti-PD-1 therapy efficacy in prostate cancer.

Ligneous periodontitis: A molecularly confirmed case of type I plasminogen deficiency.

Ligneous periodontitis: A molecularly confirmed case of type I plasminogen deficiency.

Perinatal Intracranial Hemorrhage as a Rare Presentation of Plasminogen Activator Inhibitor-1 (PAI-1) Deficiency: A Case Report.

Perinatal Intracranial Hemorrhage as a Rare Presentation of Plasminogen Activator Inhibitor-1 (PAI-1) Deficiency: A Case Report.