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Quoted phrase not found in phrase index: "Hereditary thrombophilia due to congenital protein C deficiency"
Page 1
Direct Oral Anticoagulants in Select Patients With Hypercoagulable Disorders.
Valanejad SM, Davis KA. Valanejad SM, et al. Ann Pharmacother. 2021 Jul;55(7):891-901. doi: 10.1177/1060028020968551. Epub 2020 Oct 26. Ann Pharmacother. 2021. PMID: 33100017 Review.
DATA SOURCES: An electronic PubMed literature search was conducted from January 2010 to July 2020 using the following keywords: DOAC, rivaroxaban, apixaban, dabigatran, edoxaban, thrombophilia, cancer, antiphospholipid syndrome, protein C deficiency, p …
DATA SOURCES: An electronic PubMed literature search was conducted from January 2010 to July 2020 using the following keywords: DOAC, rivaro …
Pregnancy-associated thrombosis.
Pabinger I, Grafenhofer H. Pabinger I, et al. Wien Klin Wochenschr. 2003 Aug 14;115(13-14):482-4. doi: 10.1007/BF03041032. Wien Klin Wochenschr. 2003. PMID: 13677267 Review.
In the general population the incidence of pregnancy associated VTE is approximately 1 in 1500 deliveries The risk of VTE is five times higher in a pregnant than in a non-pregnant woman. Postpartum the VTE-risk is even higher. Women with congenital abnormalities or persist …
In the general population the incidence of pregnancy associated VTE is approximately 1 in 1500 deliveries The risk of VTE is five times high …
Protein C deficiency as the major cause of thrombophilias in childhood.
Ohga S, Ishiguro A, Takahashi Y, Shima M, Taki M, Kaneko M, Fukushima K, Kang D, Hara T; Japan Childhood Thrombophilia Study Group. Ohga S, et al. Pediatr Int. 2013 Jun;55(3):267-71. doi: 10.1111/ped.12102. Pediatr Int. 2013. PMID: 23521084 Review.
Factor V Leiden (G1691A) and factor II mutation (G20210A) are the leading causes of inherited thrombophilias in Caucasians, but are not found in Asian ancestries. Protein S (PS), protein C (PC) and antithrombin (AT) activity are reportedly low in 65% of adult Japanese pati …
Factor V Leiden (G1691A) and factor II mutation (G20210A) are the leading causes of inherited thrombophilias in Caucasians, but are n …
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 …
Laboratory diagnosis of hereditary thrombophilia.
Michiels JJ, Hamulyák K. Michiels JJ, et al. Semin Thromb Hemost. 1998;24(4):309-20. doi: 10.1055/s-2007-996019. Semin Thromb Hemost. 1998. PMID: 9763348 Review.
Genetic defects of antithrombin (AT) or one of the components of the protein C pathway are associated with hereditary thrombophilia. Laboratory assays are currently available to diagnose and type hereditary thrombophilia due to deficiency or dysfunctio …
Genetic defects of antithrombin (AT) or one of the components of the protein C pathway are associated with hereditary thrombophili …
Multiple arterial and venous thromboembolism in a male patient with hereditary protein C deficiency: A case report.
Sun L, Li X, Li Q, Wang L, Li J, Shu C. Sun L, et al. Medicine (Baltimore). 2021 Apr 16;100(15):e25575. doi: 10.1097/MD.0000000000025575. Medicine (Baltimore). 2021. PMID: 33847687 Free PMC article.
RATIONALE: Hereditary protein C deficiency has a high prevalence in Asian populations, being the important risk factor associated with thrombophilia. ...LESSONS: Aggressive surgical treatment may be the effective attempt for life-saving when con …
RATIONALE: Hereditary protein C deficiency has a high prevalence in Asian populations, being the important risk …
Efficacy and safety of protein C concentrate to treat purpura fulminans and thromboembolic events in severe congenital protein C deficiency.
Manco-Johnson MJ, Bomgaars L, Palascak J, Shapiro A, Geil J, Fritsch S, Pavlova BG, Gelmont D. Manco-Johnson MJ, et al. Thromb Haemost. 2016 Jul 4;116(1):58-68. doi: 10.1160/TH15-10-0786. Epub 2016 Apr 7. Thromb Haemost. 2016. PMID: 27052576 Clinical Trial.
Severe congenital protein C (PC) deficiency (SCPCD) is associated with disseminated intravascular coagulation (DIC), purpura fulminans (PF), and vascular thromboembolic events (TE), often leading to organ failure and death. ...
Severe congenital protein C (PC) deficiency (SCPCD) is associated with disseminated intravascular coagulation (DIC), purpura fulminan …
Role of thrombophilia factors in acute systemic-pulmonary shunt obstruction.
Ergul Y, Kiplapinar N, Tanidir IC, Ozturk E, Guzeltas A, Haydin S, Akcay A, Erek E, Yeniterzi M, Odemis E, Bakir I. Ergul Y, et al. Pediatr Int. 2015 Dec;57(6):1072-7. doi: 10.1111/ped.12727. Epub 2015 Nov 10. Pediatr Int. 2015. PMID: 26096312
BACKGROUND: Systemic-pulmonary shunts are widely used in initial palliation in cyanotic congenital heart disease. The incidence and the relationship between acute shunt obstruction and thrombophilia are not precisely defined. ...Acute shunt occlusion rate was 10% (8 …
BACKGROUND: Systemic-pulmonary shunts are widely used in initial palliation in cyanotic congenital heart disease. The incidence and t …
Factor V Leiden, protein C, and lipoprotein (a) in catheter-related thrombosis in childhood: a prospective study.
Nowak-Göttl U, Dübbers A, Kececioglu D, Koch HG, Kotthoff S, Runde J, Vielhaber H. Nowak-Göttl U, et al. J Pediatr. 1997 Oct;131(4):608-12. doi: 10.1016/s0022-3476(97)70071-4. J Pediatr. 1997. PMID: 9386668
OBJECTIVE: To determine the association between catheter-related thromboses and hereditary causes of thrombophilia, including the factor V Leiden mutation, deficiencies of protein C or protein S, or increased lipoprotein (a). ...Fifteen of the 18 infants with thromb …
OBJECTIVE: To determine the association between catheter-related thromboses and hereditary causes of thrombophilia, including …
Fast functional assay of protein C in whole plasma using a snake venom activator: evaluation in patients with congenital and acquired protein C deficiencies.
Takahashi H, Hanano M, Tatewaki W, Shibata A. Takahashi H, et al. Clin Chim Acta. 1988 Jul 29;175(3):217-25. doi: 10.1016/0009-8981(88)90098-8. Clin Chim Acta. 1988. PMID: 3416483
Both anticoagulant and amidolytic activities of protein C (PC) were measured using a snake venom activator in 4 patients with hereditary PC deficiency, 37 with disseminated intravascular coagulation (DIC), and 30 under stabilized warfarin therapy. ...PC levels measured by …
Both anticoagulant and amidolytic activities of protein C (PC) were measured using a snake venom activator in 4 patients with hereditary …
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