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Quoted phrase not found in phrase index: "Hereditary thrombophilia due to congenital protein C deficiency"
Page 1
Isolated Protein C Deficiency in a Newborn.
Bencharef H, Hidki F, Lahmoudi A, Pongo C, Chemsi M, Lehlimi M, Habzi A, Benomar S, Oukkache B. Bencharef H, et al. Clin Lab. 2023 May 1;69(5). doi: 10.7754/Clin.Lab.2020.200515. Clin Lab. 2023. PMID: 37145086
BACKGROUND: Congenital protein C deficiency is a rare hereditary thrombophilia, neonatal purpura fulminans is the most serious form of this deficit. ...We use the Berichrom Protein C assay on an automated coagulation analyzer from Siemens …
BACKGROUND: Congenital protein C deficiency is a rare hereditary thrombophilia, neonatal purpura f …
Human protein C concentrates for replacement therapy in congenital and acquired protein C deficiency.
Knoebl PN. Knoebl PN. Drugs Today (Barc). 2008 Jun;44(6):429-41. doi: 10.1358/dot.2008.44.6.1217993. Drugs Today (Barc). 2008. PMID: 18596997 Review.
Hereditary severe protein C deficiency is a life-threatening state with neonatal purpura fulminans. Patients with heterozygous protein C deficiency have an increased risk for thromboembolic events or coumarin-induced skin necrosis. …
Hereditary severe protein C deficiency is a life-threatening state with neonatal purpura fulminans. Patients wit …
Incidence and clinical characteristics of hereditary disorders associated with venous thrombosis.
Tabernero MD, Tomas JF, Alberca I, Orfao A, Lopez Borrasca A, Vicente V. Tabernero MD, et al. Am J Hematol. 1991 Apr;36(4):249-54. doi: 10.1002/ajh.2830360405. Am J Hematol. 1991. PMID: 1826407
At present, different congenital defects in several proteins--antithrombin III (AT III), protein C (PC), protein S (PS), and plasminogen (PLG)--are known to be causes of hereditary predisposition to thrombosis (thrombophilia). The incidence of these heredi …
At present, different congenital defects in several proteins--antithrombin III (AT III), protein C (PC), protein S (PS), and plasmino …
Studies on congenital protein C deficiency in Japanese: prevalence, genetic analysis, and relevance to the onset of arterial occlusive diseases.
Sakata T, Kario K, Katayama Y, Matsuyama T, Kato H, Miyata T. Sakata T, et al. Semin Thromb Hemost. 2000;26(1):11-6. doi: 10.1055/s-2000-9796. Semin Thromb Hemost. 2000. PMID: 10805275
Hereditary protein C deficiency is associated with a predisposition to venous thrombosis. ...The observed prevalence of protein C deficiency was 1 per 620. We performed genetic analyses of 57 Japanese families with protei …
Hereditary protein C deficiency is associated with a predisposition to venous thrombosis. ...The observed …
A protein C and plasminogen compound heterozygous mutation and a compound heterozygote of protein C in two related Chinese families.
Cheng X, Wang M, Jiang M, Bhugul PA, Hao X, Yang L. Cheng X, et al. Blood Coagul Fibrinolysis. 2016 Oct;27(7):838-844. doi: 10.1097/MBC.0000000000000579. Blood Coagul Fibrinolysis. 2016. PMID: 27314862
Hereditary protein C (PC) deficiency and congenital plasminogen (PLG) deficiency are both factors of thrombophilia which were caused by PC and PLG gene mutations with the characteristics of activity and antigen decreasing inconsonantly. ...Genetic analysis de …
Hereditary protein C (PC) deficiency and congenital plasminogen (PLG) deficiency are both factors of thrombophilia whic …