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Last Updated: 01/07/2026
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Found 90 publications
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
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
Last Updated: 01/07/2026