Stephanie Curcio PT
Physical Therapist (Pediatric) | Pediatrics
382 S MAIN ST CHESHIRE CT, 06410About
Stephanie Curcio is a pediatric physical therapist practicing in CHESHIRE, CT. Stephanie is a doctor specializing in physical treatment of children to help reduce pain, restore mobility, rehabilitate an injury, or increase movement and overall function. As a physical therapist, Dr. Curcio can treat multiple conditions with exercises, ultrasound, electrical stimulation, joint mobilization, heat, ice, massage, laser or light therapy and more. Dr. Curcio will create a treatment plan based on the childs specific injury, disease or condition, and might target a specific body part or body system based on the individual.
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Expert Publications
Data provided by the National Library of Medicine- Surveillance for factor VIII inhibitor development in the Canadian Hemophilia A population following the widespread introduction of recombinant factor VIII replacement therapy.
- Proteolytic processing of human coagulation factor IX by plasmin.
- Aortic endothelial cell von Willebrand factor content, and circulating
- Waveform analysis of clotting test optical profiles in the diagnosis and management of disseminated intravascular coagulation (DIC).
- Effectiveness of factor VIII infusions in haemophilia A patients with high responding inhibitors.
- Anticoagulant and fibrinolytic activities are promoted, not retarded, in vivo after thrombin generation in the presence of a monoclonal antibody that inhibits activation of protein C.
- Normalization of the haemostatic plugs of dogs with haemophilia A (factor VIII deficiency) following the infusion of a combination of factor Xa and phosphatidylcholine/phosphatidylserine vesicles.
- The measurement of low levels of factor VIII or factor IX in hemophilia A and hemophilia B plasma by clot waveform analysis and thrombin generation assay.
- Alpha 2-macroglobulin binds and inhibits activated protein C.
- Germ-line mosaicism for a valine-to-methionine substitution at residue 553 in the glycoprotein Ib-binding domain of von Willebrand factor, causing type IIB von Willebrand disease.
- Recurring mutations at CpG dinucleotides in the region of the von Willebrand factor gene encoding the glycoprotein Ib binding domain, in patients with type IIB von Willebrand's disease.
- Activated thrombin-activatable fibrinolysis inhibitor is generated in vivo at levels that can substantially affect fibrinolysis in chimpanzees in response to thrombin generation.
- The effect of plasma von Willebrand factor on the binding of human factor VIII to thrombin-activated human platelets.
- Organization of a hemophilia genetic screening program. Ontario Hemophilia Study Group.
- The role of factor VII in haemostasis: infusion studies of factor VIIa in a canine model of factor VIII deficiency.
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