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Last Updated: 10/31/2025

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Found 352 publications

Measurement of cleaved high-molecular-weight kininogen in patients with hereditary angioedema due to C1-inhibitor deficiency: preanalytical and analytical optimization.

Measurement of cleaved high-molecular-weight kininogen in patients with hereditary angioedema due to C1-inhibitor deficiency: preanalytical and analytical optimization.

Journal: Journal of immunological methods
Published: May 12, 2025

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.

Journal: Cureus
Published: February 19, 2025

Advances in the Pathogenesis of Hereditary Angioedema.

Advances in the Pathogenesis of Hereditary Angioedema.

Journal: Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae
Published: January 08, 2025

Identification of multiple novel procoagulant plasma ligands for stabilin-2.

Identification of multiple novel procoagulant plasma ligands for stabilin-2.

Journal: Journal of thrombosis and haemostasis : JTH
Published: December 27, 2024

Factor XI and Atrial Fibrillation: A Mismatched Pairing?

Factor XI and Atrial Fibrillation: A Mismatched Pairing?

Journal: European cardiology
Published: December 26, 2024

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.

Journal: Ochsner journal
Published: December 25, 2024

Hereditary Angioedema With Normal C1 Inhibitor: A Quarter Century of Forward Progress and Persisting Obstacles.

Hereditary Angioedema With Normal C1 Inhibitor: A Quarter Century of Forward Progress and Persisting Obstacles.

Journal: The journal of allergy and clinical immunology. In practice
Published: December 16, 2024

KNG1 mutations (c.618 T > G and c.1165C > T) cause disruption of the Cys206-Cys218 disulfide bond and truncation of the D5 domain leading to hereditary high molecular weight kininogen deficiency.

KNG1 mutations (c.618 T > G and c.1165C > T) cause disruption of the Cys206-Cys218 disulfide bond and truncation of the D5 domain leading to hereditary high molecular weight kininogen deficiency.

Journal: Clinical biochemistry
Published: October 03, 2024

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

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: September 01, 2024

Hereditary angioedema plasma proteomics following specific plasma kallikrein inhibition with lanadelumab.

Hereditary angioedema plasma proteomics following specific plasma kallikrein inhibition with lanadelumab.

Journal: Frontiers in immunology
Published: July 31, 2024

Case Report: Allelic and biallelic variants in coagulation factor XI cause factor XI deficiency.

Case Report: Allelic and biallelic variants in coagulation factor XI cause factor XI deficiency.

Journal: Frontiers in cardiovascular medicine
Published: July 09, 2024

Contact System Activation and Bradykinin Generation in Angioedema: Laboratory Assessment and Biomarker Utilization.

Contact System Activation and Bradykinin Generation in Angioedema: Laboratory Assessment and Biomarker Utilization.

Journal: Immunology and allergy clinics of North America
Published: June 27, 2024
Showing 1-12 of 352

Last Updated: 10/31/2025