Instructor in Pediatrics, Dana-Farber Cancer Institute
Pediatric Hematology & Oncology
Dr. Cameron C. Trenor III, MD
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Cameron C. Trenor III, MD practices Pediatric Hematology & Oncology. He went to University of Tennessee College of Medicine. Cameron Trenor is also a published MD. He has 26 paper published. The most recent paper is: The G185R mutation disrupts function of the iron transporter Nramp2.
Publications
- Efficacy and Safety of Sirolimus in the Treatment of Complicated Vascular Anomalies.
- Comment on: Steroid-resistant kaposiform hemangioendothelioma: A retrospective study of 37 patients treated with vincristine and long-term follow-up.
- Cutaneovisceral Angiomatosis with Thrombocytopenia without Cutaneous Involvement.
- Complex lymphatic anomalies.
- Thromboprophylaxis of Hospitalized Pediatric Patients With IBD is Safe and Should Be Considered.
- High incidence of catheter-associated venous thromboembolic events in patients with long gap esophageal atresia treated with the Foker process.
- Hypercoagulability panel testing predicts Thrombosis in neonates undergoing cardiac surgery.
- Hypercoagulability Markers Predict Thrombosis in Single Ventricle Neonates Undergoing Cardiac Surgery.
- Kaposiform hemangioendothelioma: atypical features and risks of Kasabach-Merritt phenomenon in 107 referrals.
- Novel microfluidic platform for automated lab-on-chip testing of hypercoagulability panel.
- Sirolimus for refractory vascular anomalies.
- Tissue factor-bearing microparticles and thrombus formation.
- Hormonal contraception and thrombotic risk: a multidisciplinary approach.
- Thrombosis and inflammatory bowel disease: a call for improved awareness and prevention.
- Thrombophilia and pediatric stroke.
- Venous Thrombosis associated with gene deletion of tissue factor pathway inhibitor.
- A mutation in Sec15l1 causes Anemia in hemoglobin deficit (hbd) mice.
- Microcytic anaemia mice have a mutation in Nramp2, a candidate iron transporter gene.
- The Boston Marathon Study: a novel approach to research during residency.
- Thrombosis and thrombophilia: principles for pediatric patients.
- The molecular defect in hypotransferrinemic mice.
- A mutation in a mitochondrial transmembrane protein is responsible for the pleiotropic hematological and skeletal phenotype of flexed-tail (f/f) mice.
- Autosomal-dominant hemochromatosis is associated with a mutation in the ferroportin (SLC11A3) gene.
- The G185R mutation disrupts function of the iron transporter Nramp2.
- Novel bacterial P-type ATPases with histidine-rich heavy-metal-associated sequences.
Schools
University of Tennessee Memphis College of Medicine amp Surgery
Children39s Hospital Boston
Dana Farber Cancer Institute
Conditions Treated
- Anemia
- Deep Vein Thrombosis (DVT)
- Hypercoagulable State
- Immune Thrombocytopenic Purpura (ITP)
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Doctors Specialties
- Pediatric Hematology
- Oncology
Accepted Insurances
- Blue Card PPO
- BlueConnect HMO
- Blue with Managed Care Behavioral Health HMO
- Preferred Blue PPO
- Cigna HMO
- Cigna PPO
- Great West Healthcare-Cigna PPO
- LocalPlus
- Open Access Plus
- Commercial Insurance Company
- GHI PPO
- Fallon Community Health Plan
- First Health (Coventry Health Care) PPO
- Choice Care PPO
- Medicare MCR
- MultiPlan PPO
- PHCS Network PPO
- Tufts PPO
- Choice Plus POS
- Navigate HMO
- Navigate POS
- Options PPO
- United Healthcare
Education
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Boston Children's Hospital -
University of Tennessee College of Medicine
Hospital
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Dana-Farber Cancer Institute
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