Disease: Congenital thrombotic disease- due to Protein C deficiency
- A case of multiple cerebral arterial thrombosis due to congenital protein C deficiency
- A case of recurrent cerebral vein thrombosis with protein C gene mutation identified
- A case of superior mesenteric venous thrombosis due to protein C deficiency in a patient with duodenal ulcer bleeding
- A homozygous deletion/insertion mutation in the protein C (PROC) gene causing neonatal Purpura fulminans: prenatal diagnosis in an at-risk pregnancy
- Acquired Versus Congenital Neonatal Purpura Fulminans: A Case Report and Literature Review
- Acroangiodermatitis of Mali in protein C deficiency due to a novel PROC gene mutation
- Adult-onset arterial thrombosis in a pedigree of homozygous and heterozygous protein C deficiency
- An imbalance of pro- vs anti-coagulation factors in plasma from patients with cirrhosis
- Analysis of 45 episodes of arterial occlusive disease in Japanese patients with congenital protein C deficiency
- Antepartum findings in fetal protein C deficiency
- Aortic Mural Thrombus Associated with Congenital Protein C Deficiency in an Elderly Patient
- Arteriovenous thrombosis in chronic renal failure patients receiving renal replacement therapy
- Association of congenital protein C deficiency and latent myeloproliferative disease as cause of splanchnic venous thrombosis in a 34-year-old woman
- Blood coagulation disorders--special reference to thrombosis
- Cerebral venous thrombosis in children
- Clinical Characteristics and Outcome of Budd-Chiari Syndrome at a Tertiary Care Hospital in Pakistan
- Clinical manifestations and management of inherited thrombophilia: retrospective analysis and follow-up after diagnosis of 238 patients with congenital deficiency of antithrombin III, protein C, protein S
- Coagulation factor abnormalities as possible thrombotic risk factors after Fontan operations
- Congenital deficiencies of natural anticoagulant systems responsible for recurrent thromboembolism
- Congenital heterozygous protein C deficiency with portal vein thrombosis
- Congenital protein C deficiency and thrombosis in a dog
- Congenital protein C deficiency and thrombotic disease in nine French families
- Congenital protein C deficiency in patients with thromboembolic disease. Study of 4 Spanish families
- Congenital prothrombotic disorders in children with peripheral venous and arterial thromboses
- Congenital thrombophilia among patients with venous thromboembolism
- Congenital thrombophilia caused by protein C deficiency
- Congenital thrombotic diseases
- Deep vein thrombosis due to protein C deficiency in a neonate
- Deep venous thrombosis treated by rivaroxaban in a young patient with type Ia carbohydrate-deficient glycoprotein (CDG) syndrome
- Different incidence of venous thrombosis in patients with inherited deficiencies of antithrombin III, protein C and protein S
- Direct Oral Anticoagulants in Select Patients With Hypercoagulable Disorders
- Efficacy and safety of protein C concentrate to treat purpura fulminans and thromboembolic events in severe congenital protein C deficiency
- Ethnic differences in coagulation factor abnormalities after the Fontan procedure
- Factor V Leiden, protein C, and lipoprotein (a) in catheter-related thrombosis in childhood: a prospective study
- Fetal hydrocephalus and neonatal stroke as the first presentation of protein C deficiency
- Gene targeting in hemostasis. factor XI
- Hematological causes of venous thrombosis in young people: high incidence of myeloproliferative disorder as underlying disease in patients with splanchnic venous thrombosis
- Heterozygous protein C deficiency associated with multiple congenital hemangiomas--a case report
- Homozygous protein C deficiency combined with heterozygous dysplasminogenemia found in a 21-year-old thrombophilic male
- Homozygous type I protein C deficiency in two unrelated families exhibiting thrombophilia related to Ala136-->Pro or Arg286-->His mutations
- Homozygous type I protein C deficiency in two unrelated families exhibiting thrombophilia related to Ala136-->Pro or Arg286-->His mutations
- Incidence and clinical characteristics of hereditary disorders associated with venous thrombosis
- Inherited protein-C deficiency, factor V G 1691 A and FV A 4070 G mutations in a child with internal cerebral venous thrombosis
- Inherited thrombophilia and arterial diseases
- Intracardiac thrombosis diagnosed by echocardiography in childhood: predisposing and etiological factors
- Liver transplantation for congenital protein C deficiency with initial poor graft function: a case report with literature review
- Long-term Outcome of Budd-Chiari Syndrome: A Single Center Experience
- MiR-124 and miR-506 are involved in the decline of protein C in children with extra-hepatic portal vein obstruction
- Multiple arterial and venous thromboembolism in a male patient with hereditary protein C deficiency: A case report
- Neonatal purpura fulminans due to homozygous protein C or protein S deficiencies
- Ophthalmic manifestation of congenital protein C deficiency
- Paediatric presentation and outcome of congenital protein C deficiency in Japan
- Pediatric venous thromboembolic disease in one single center: congenital prothrombotic disorders and the clinical outcome
- Perioperative management for fracture in a child with homozygous congenital protein C deficiency
- Physiopathologic and clinical implications of protein C deficiencies
- Postpartum cerebral venous thrombosis, congenital protein C deficiency, and activated protein C resistance due to heterozygous factor V Leiden mutation
- Pregnancy-associated thrombosis
- Prevalence of prothrombotic abnormalities in patients with acute mesenteric ischemia
- Prevalence, Genetic Background, and Clinical Phenotype of Congenital Thrombophilia in Chronic Thromboembolic Pulmonary Hypertension
- PROC c.574_576del polymorphism: a common genetic risk factor for venous thrombosis in the Chinese population
- Protein C activity in severely ill newborns with congenital heart disease
- Protein C in thromboembolic disease
- Protein C pathway in infants and children
- Prothrombotic risk factors in children with hemiplegic cerebral palsy
- Pseudothromboangiitis obliterans and qualitative protein C deficiency: report of a case
- Purpura fulminans. A cutaneous manifestation of severe protein C deficiency
- Recent advances in understanding clotting and evaluating patients with recurrent thrombosis
- Rivaroxaban dose adjustment using thrombin generation in severe congenital protein C deficiency and warfarin-induced skin necrosis
- Role of thrombophilia factors in acute systemic-pulmonary shunt obstruction
- Searching for genetic variants associated with thrombophilia
- Severe inherited "homozygous" protein C deficiency in a newborn infant
- Severe protein C deficiency in congenital thrombotic disease--description of an immunoenzymological assay for protein C determination
- Silent cerebral infarcts in basal ganglia are advanced in congenital protein C-deficient heterozygotes with hypertension
- Specific sequelae after Fontan operation at mid- and long-term follow-up. Arrhythmia, liver dysfunction, and coagulation disorders
- Studies on congenital protein C deficiency in Japanese: prevalence, genetic analysis, and relevance to the onset of arterial occlusive diseases
- Superior sagittal sinus and cerebral cortical venous thrombosis caused by congenital protein C deficiency--case report
- Syndromes of thrombosis and hypercoagulability. Congenital and acquired causes of thrombosis
- The "pseudo-cholangiocarcinoma sign" in patients with cavernous transformation of the portal vein and its effect on the serum alkaline phosphatase and bilirubin levels
- The etiologic distribution of thrombophilic factors in chronic portal vein thrombosis
- The use of a functional and immunologic assay for plasma protein C in the study of the heterogeneity of congenital protein C deficiency
- Thrombogenic diseases
- Thrombophilia caused by congenital disorders of blood coagulation
- Thrombophilia found in patients with moyamoya disease
- Thrombophilia in patients with venous thromboembolism
- Thrombophilia: disorders predisposing to venous thromboembolism
- Thrombosis in congenital deficiencies of AT III, protein C or protein S: a study of 44 children
- Thyroid crisis and protein C deficiency in a case of superior sagittal sinus thrombosis
- Two-dimensional echocardiographic diagnosis of tricuspid valve noninfective endocarditis due to protein C deficiency (lesion mimicking tricuspid valve myxoma)
- Unmasking Asian thrombophilia: is APC dysfunction the real culprit?