Protein C Deficiency Latest Advances
Find the Latest Research About Protein C Deficiency
Last Updated: 04/28/2026
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Found 1899 publications
Clinical and genetic analysis of two families with combined defect in antithrombin and protein C genes
Journal: Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi
Published: March 16, 2026
Congenital Protein C Deficiency Presenting as Neonatal Purpura Fulminans: A Report of Two Cases.
Journal: Cureus
Published: February 16, 2026
Inherited Thrombophilia as a Risk Factor for Persistent Left Ventricular Thrombus Following Acute Myocardial Infarction.
Journal: Thrombosis and haemostasis
Published: February 09, 2026
Plasma-derived human protein C replacement concentrate therapy in a patient with severe congenital protein C deficiency presenting with purpura fulminans and disseminated intravascular coagulation
Journal: [Rinsho ketsueki] The Japanese journal of clinical hematology
Published: February 01, 2026
Pulmonary Embolism Presenting as Recurrent Syncope and Visual Disturbances in a Patient With Protein C Deficiency: An Atypical Emergency Department Presentation.
Journal: Cureus
Published: December 20, 2025
Corrigendum to 'Real-world use of protein C concentrate for the treatment of patients with protein C deficiency: an international registry': [Journal of Thrombosis and Haemostasis 23(11) (2025) 3569-3577].
Journal: Journal of thrombosis and haemostasis : JTH
Published: December 19, 2025
Assessing the Correlation of Protein C and Protein S Levels with Stroke Severity and Functional Outcomes in Adults with Ischaemic Stroke.
Journal: West African journal of medicine
Published: December 10, 2025
Purpura Fulminans Due to Escherichia coli Septicemia in Relapsed Acute Myeloid Leukemia: An Unusual Case of Protein C Deficiency and Disseminated Intravascular Coagulation.
Journal: Cureus
Published: November 27, 2025
Diagnosing thrombophilia: the case for genetic or functional testing?
Journal: Expert review of molecular diagnostics
Published: November 10, 2025
A pedigree analysis of deep venous thrombosis caused by rare compound heterozygous PROC mutations combined with a heterozygous THBD mutation.
Journal: Thrombosis journal
Published: November 06, 2025
FDA-approved drug repurposing in zebrafish identifies thyroid hormone and other compounds as potential antithrombotics.
Journal: bioRxiv : the preprint server for biology
Published: October 03, 2025
Last Updated: 04/28/2026