Prekallikrein Deficiency Latest Advances

Coagulation management in endovascular aortic repair in a patient with congenital prekallikrein deficiency: a case report.

Journal: Anaesthesia and intensive care

Published: October 22, 2025

A Case of Severe Prekallikrein Deficiency Manifesting as Isolated Activated Partial Thromboplastin Time (aPTT) Prolongation.

Journal: Cureus

Published: February 19, 2025

Rare Prekallikrein Deficiency Identified During Workup of Isolated Prolonged Activated Partial Thromboplastin Time.

Journal: Ochsner journal

Published: December 25, 2024

Analysis of two consanguineous Chinese pedigrees affected with Hereditary prokallikrein deficiency and High molecular weight kininogen deficiency

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: September 01, 2024

Genetic Analysis of Prekallikrein Deficiency in a Consanguineously Married Chinese Family.

Journal: Turkish journal of haematology : official journal of Turkish Society of Haematology

Published: December 05, 2023

Factor XII and prekallikrein promote microvascular inflammation and psoriasis in mice.

Journal: British journal of pharmacology

Published: July 17, 2023

Prekallikrein deficiency: Challenges in laboratory testing.

Journal: International journal of laboratory hematology

Published: February 14, 2022

Definite diagnosis of plasma prekallikrein deficiency should not be based exclusively on shortening of the aPTT upon prolonged pre-incubation.

Journal: International journal of laboratory hematology

Published: December 15, 2021

Prekallikrein deficiency due to homozygous KLKB1(+) mutation c.444_445insT (p.Ser151PhefsTer34).

Journal: International journal of laboratory hematology

Published: October 13, 2021

A Rare Cause of Isolated Prolonged Activated Partial Thromboplastin Time: An Overview of Prekallikrein Deficiency and the Contact System.

Journal: Journal of investigative medicine high impact case reports

Published: May 04, 2021

Homozygous Prekallikrein Deficiency in the USA: Several Patients but Still Few Mutation Studies.

Journal: Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis

Published: March 03, 2021

Resolving Differential Diagnostic Problems in von Willebrand Disease, in Fibrinogen Disorders, in Prekallikrein Deficiency and in Hereditary Hemorrhagic Telangiectasia by Next-Generation Sequencing.

Journal: Life (Basel, Switzerland)

Published: February 05, 2021

Prekallikrein Deficiency Latest Advances

Find the Latest Research About Prekallikrein Deficiency

Coagulation management in endovascular aortic repair in a patient with congenital prekallikrein deficiency: a case report.

Coagulation management in endovascular aortic repair in a patient with congenital prekallikrein deficiency: a case report.

A Case of Severe Prekallikrein Deficiency Manifesting as Isolated Activated Partial Thromboplastin Time (aPTT) Prolongation.

A Case of Severe Prekallikrein Deficiency Manifesting as Isolated Activated Partial Thromboplastin Time (aPTT) Prolongation.

Rare Prekallikrein Deficiency Identified During Workup of Isolated Prolonged Activated Partial Thromboplastin Time.

Rare Prekallikrein Deficiency Identified During Workup of Isolated Prolonged Activated Partial Thromboplastin Time.

Analysis of two consanguineous Chinese pedigrees affected with Hereditary prokallikrein deficiency and High molecular weight kininogen deficiency

Analysis of two consanguineous Chinese pedigrees affected with Hereditary prokallikrein deficiency and High molecular weight kininogen deficiency

Genetic Analysis of Prekallikrein Deficiency in a Consanguineously Married Chinese Family.

Genetic Analysis of Prekallikrein Deficiency in a Consanguineously Married Chinese Family.

Factor XII and prekallikrein promote microvascular inflammation and psoriasis in mice.

Factor XII and prekallikrein promote microvascular inflammation and psoriasis in mice.

Prekallikrein deficiency: Challenges in laboratory testing.

Prekallikrein deficiency: Challenges in laboratory testing.

Definite diagnosis of plasma prekallikrein deficiency should not be based exclusively on shortening of the aPTT upon prolonged pre-incubation.

Definite diagnosis of plasma prekallikrein deficiency should not be based exclusively on shortening of the aPTT upon prolonged pre-incubation.

Prekallikrein deficiency due to homozygous KLKB1(+) mutation c.444_445insT (p.Ser151PhefsTer34).

Prekallikrein deficiency due to homozygous KLKB1(+) mutation c.444_445insT (p.Ser151PhefsTer34).

A Rare Cause of Isolated Prolonged Activated Partial Thromboplastin Time: An Overview of Prekallikrein Deficiency and the Contact System.

A Rare Cause of Isolated Prolonged Activated Partial Thromboplastin Time: An Overview of Prekallikrein Deficiency and the Contact System.

Homozygous Prekallikrein Deficiency in the USA: Several Patients but Still Few Mutation Studies.

Homozygous Prekallikrein Deficiency in the USA: Several Patients but Still Few Mutation Studies.

Resolving Differential Diagnostic Problems in von Willebrand Disease, in Fibrinogen Disorders, in Prekallikrein Deficiency and in Hereditary Hemorrhagic Telangiectasia by Next-Generation Sequencing.

Resolving Differential Diagnostic Problems in von Willebrand Disease, in Fibrinogen Disorders, in Prekallikrein Deficiency and in Hereditary Hemorrhagic Telangiectasia by Next-Generation Sequencing.