Cameron C Trenor 3rd
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Explore the profile of Cameron C Trenor 3rd including associated specialties, affiliations and a list of published articles.
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54
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1312
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Recent Articles
11.
Wang K, Glenn R, Adams D, Alomari A, Al-Ibraheemi A, Anderson M, et al.
J Pediatr Orthop
. 2019 Jun;
40(3):e227-e236.
PMID: 31181028
Background: Fibroadipose vascular anomaly (FAVA) is a recently-defined vascular malformation often involving the extremities and presenting in childhood. Patients may present to orthopaedic surgeons with pain, swelling, joint contractures, and...
12.
Doody J, Adil E, Trenor 3rd C, Cunningham M
Ann Otol Rhinol Laryngol
. 2019 Jun;
128(11):1061-1072.
PMID: 31148463
Objective: Juvenile nasopharyngeal angiofibroma (JNA) is a rare vascular tumor of unknown etiology. Studies investigating the molecular and genetic determinants of JNA are limited by small sample size and inconsistent...
13.
Taghinia A, Upton J, Trenor 3rd C, Alomari A, Lillis A, Shaikh R, et al.
J Pediatr Surg
. 2018 Oct;
54(3):562-568.
PMID: 30292452
Background: Central conducting lymphatic anomalies (CCLA) may cause chylous leaks and protein-losing enteropathy (PLE) owing to dysfunction of the central lymphatic channels. Most of the treatment strategies for these conditions...
14.
Iacobas I, Phung T, Adams D, Trenor 3rd C, Blei F, Fishman D, et al.
J Pediatr
. 2018 Sep;
203:294-300.e2.
PMID: 30244993
Objective: To define the types of hepatic hemangiomas using the updated International Society for the Study of Vascular Anomalies classification and to create a set of guidelines for their diagnostic...
15.
Mo A, Trenor 3rd C, Hedequist D
JBJS Case Connect
. 2018 Sep;
8(3):e70.
PMID: 30211713
Case: Gorham-Stout disease (GSD) is a rare entity that is marked by progressive osteolysis and bone resorption. A 14-year-old boy who was being followed for scoliosis presented with a marked...
16.
Reis 3rd J, Alomari A, Trenor 3rd C, Adams D, Fishman S, Spencer S, et al.
J Vasc Surg Venous Lymphat Disord
. 2018 Jun;
6(4):511-516.
PMID: 29909856
Objective: Patients with Klippel-Trénaunay syndrome (KTS) and congenital lipomatous overgrowth, vascular malformations, epidermal nevi, and spinal/skeletal abnormalities (CLOVES) syndrome have central phlebectasia and enlarged persistent embryonic veins that are often...
17.
Oladunjoye O, Sleeper L, Nair A, Trenor 3rd C, VanderPluym C, Kheir J, et al.
J Thorac Cardiovasc Surg
. 2018 May;
156(1):332-340.e1.
PMID: 29709361
Objectives: Anticoagulation with unfractionated heparin (UFH) after pediatric cardiac surgery can be monitored using either activated partial thromboplastin time (aPTT) or anti-factor Xa activity (anti-Xa). However, correlation of bleeding with...
18.
Nair A, Oladunjoye O, Trenor 3rd C, LaRonde M, van den Bosch S, Sleeper L, et al.
J Thorac Cardiovasc Surg
. 2018 May;
156(1):343-352.e4.
PMID: 29706371
Background: Patients undergoing surgery for congenital heart disease are at high risk for bleeding as well as thrombosis in the postoperative period. The objective of the study was to describe...
19.
Bernson-Leung M, Boyd T, Meserve E, Danehy A, Kapur K, Trenor 3rd C, et al.
J Pediatr
. 2018 Feb;
195:39-47.e5.
PMID: 29397159
Objective: To assess the association of placental abnormalities with neonatal stroke. Study Design: This retrospective case-control study at 3 academic medical centers examined placental specimens for 46 children with neonatal...
20.
Strychowsky J, Rahbar R, OHare M, Irace A, Padua H, Trenor 3rd C
Laryngoscope
. 2017 Aug;
128(1):269-276.
PMID: 28782106
Objective: Lymphatic malformations (LMs) are challenging to manage, particularly those involving the cervicofacial region and airway. Traditional therapy is sclerotherapy and/or resection. We aim to establish the emerging therapeutic role...