Protein C deficiency: Report of a challenging case with recurrent multiorgan thrombosis. [PDF]
Afghani R, Gharib H, Kor F, Kharazm P.
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The lost chILD: a case report of delayed diagnosis of surfactant protein C deficiency in a 15-year-old African male. [PDF]
Faelli N +11 more
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[Clinical characteristics and gene mutation analysis of two families with hereditary protein C deficiency]. [PDF]
Zeng ML +6 more
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Challenges in managing severe homozygous protein c deficiency: a case report. [PDF]
Almatter E +4 more
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Compound heterozygous protein C deficiency with pulmonary embolism caused by a novel PROC gene mutation: Case report and literature review. [PDF]
Zhang Z, Yang Z, Chen M, Li Y.
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Compound heterozygous congenital protein C deficiency: a challenging management with recurrent purpura fulminans treated with protein C concentrations. [PDF]
Srichumpuang C +3 more
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Paracentral Acute Middle Maculopathy and Nonischemic Central Retinal Vein Obstruction in a Young Patient with Protein C Deficiency. [PDF]
Abrishami M +3 more
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Protein C deficiency with recurrent systemic thrombosis associated with compound heterozygous PROC missense variants. [PDF]
Shiba M +6 more
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Lens-sparing vitrectomy for pediatric tractional retinal detachment in homozygous protein C deficiency. [PDF]
Alowairdhi MA +3 more
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Protein C deficiency with venous and arterial thromboembolic events. [PDF]
Zhang N +4 more
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