Coumarin skin necrosis without protein C deficiency.
Aust N Z J Med. 1986.
PMID: 2948486
No abstract available.
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10
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found by citation matching
Coumarin necrosis associated with hereditary protein C deficiency.
Ann Intern Med. 1984.
PMID: 6547283
No abstract available.
Coumarin necrosis, neonatal purpura fulminans, and protein C deficiency.
Arch Dermatol. 1987.
PMID: 2961308
Review.
Search results
Page 1
Coumarin necrosis, neonatal purpura fulminans, and protein C deficiency.
Arch Dermatol. 1987 Dec;123(12):1701a-1706a.
Arch Dermatol. 1987.
PMID: 2961308
Review.
Symptomatic heterozygous PC deficiency and PS deficiency have been treated with oral anticoagulants, successfully minimizing recurrence of thrombosis. Coumarin-induced skin necrosis, a rare complication of oral anticoagulant therapy usually seen within three to five …
Symptomatic heterozygous PC deficiency and PS deficiency have been treated with oral anticoagulants, successfully minimizing recurrence of t …
Protein C antigen deficiency and warfarin necrosis.
Am J Clin Pathol. 1986 Nov;86(5):653-5. doi: 10.1093/ajcp/86.5.653.
Am J Clin Pathol. 1986.
PMID: 3776917
Recent reports have suggested a correlation between congenital protein C deficiency and tissue necrosis complicating oral anticoagulants (warfarin necrosis). ...These results confirm that low protein C antigen levels are implicated in the pathog …
Recent reports have suggested a correlation between congenital protein C deficiency and tissue necrosis complica …
Human protein C concentrates for replacement therapy in congenital and acquired protein C deficiency.
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 necros …
Hereditary severe protein C deficiency is a life-threatening state with neonatal purpura fulminans. Patients with heter …
Inherited protein C deficiency and coumarin-responsive chronic relapsing purpura fulminans in a newborn infant.
Lancet. 1983 Nov 19;2(8360):1165-8. doi: 10.1016/s0140-6736(83)91216-3.
Lancet. 1983.
PMID: 6139528
A coumarin-responsive chronic relapsing purpura fulminans syndrome is described in a protein-C-deficient newborn infant. ...This experience suggests that protein C deficiency may greatly compromise the ability of newborn infants to control consumptive …
A coumarin-responsive chronic relapsing purpura fulminans syndrome is described in a protein-C-deficient newborn infant. ...This expe …
Hereditary protein C deficiency.
Haemostasis. 1985;15(4):233-40. doi: 10.1159/000215154.
Haemostasis. 1985.
PMID: 3840112
Hereditary protein C deficiency, which is inherited as an autosomal-dominant trait, predisposes to venous thrombotic disease. ...Other manifestations are cerebral venous thrombosis and mesenteric vein thrombosis. In severe, often homozygous, protein …
Hereditary protein C deficiency, which is inherited as an autosomal-dominant trait, predisposes to venous thrombotic di …
The dermatologist and protein C.
J Am Acad Dermatol. 1988 Nov;19(5 Pt 1):904-7. doi: 10.1016/s0190-9622(88)80374-8.
J Am Acad Dermatol. 1988.
PMID: 3056998
Review.
No abstract available.
Heterozygous protein C deficiency and coumarin necrosis of the skin.
Rom J Intern Med. 1992 Apr-Jun;30(2):105-11.
Rom J Intern Med. 1992.
PMID: 1496262
An obese female patient aged 47 with a personal and familial history of recurrent venous thrombosis, who developed a coumarin-induced skin necrosis is presented. Laboratory investigations, performed three months after the acute event and in absence of coumarin …
An obese female patient aged 47 with a personal and familial history of recurrent venous thrombosis, who developed a coumarin-induced …
Warfarin-Induced Skin Necrosis in Patients With Low Protein C Levels.
Acta Med Iran. 2016 Aug;54(8):551-554.
Acta Med Iran. 2016.
PMID: 27701728
Free article.
Warfarin-induced skin necrosis (WISN) is a rare complication of anticoagulant therapy associated with a high incidence of morbidity and mortality requiring immediate drug cessation. ...He had intermittent atrial fibrillation and was started on anticoagulant therapy. After …
Warfarin-induced skin necrosis (WISN) is a rare complication of anticoagulant therapy associated with a high incidence of morbidity a …
Coumarin-induced skin necrosis.
Arch Dermatol. 1993 Jun;129(6):766-8.
Arch Dermatol. 1993.
PMID: 8507082
No abstract available.
Severe congenital protein C deficiency: the use of protein C concentrates (human) as replacement therapy for life-threatening blood-clotting complications.
Biologics. 2008 Jun;2(2):285-96. doi: 10.2147/btt.s1954.
Biologics. 2008.
PMID: 19707361
Free PMC article.
Patients with heterozygous protein C deficiency have an increased risk for thromboembolic events or experience coumarin-induced skin necrosis during initiation of coumarin therapy. ...This article summarizes the current knowledge on prote …
Patients with heterozygous protein C deficiency have an increased risk for thromboembolic events or experience couma …
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