Owase Jeelani
Overview
Explore the profile of Owase Jeelani including associated specialties, affiliations and a list of published articles.
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Articles
23
Citations
165
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Recent Articles
1.
Deliege L, Carriero A, Ong J, James G, Jeelani O, Dunaway D, et al.
Comput Biol Med
. 2024 May;
177:108633.
PMID: 38805810
Background: Endoscopic strip craniectomy followed by helmet therapy (ESCH) is a minimally invasive approach for correcting sagittal craniosynostosis. The treatment involves a patient-specific helmet designed to facilitate lateral growth while...
2.
Heutinck P, Knoops P, Florez N, Biffi B, Breakey W, James G, et al.
J Craniomaxillofac Surg
. 2021 Mar;
49(6):449-455.
PMID: 33712336
The aim of this study is, firstly, to create a population-based 3D head shape model for the 0 to 2-year-old subjects to describe head shape variability within a normal population...
3.
Bozkurt S, Borghi A, Jeelani O, Dunaway D, Schievano S
J Craniofac Surg
. 2020 Jan;
31(3):692-696.
PMID: 31977684
Unicoronal craniosynostosis is the second most common type of nonsyndromic craniosynostosis: it is characterized by ipsilateral forehead and fronto-parietal region flattening with contralateral compensatory bossing. It is a complex condition;...
4.
Borghi A, Florez N, Ruggiero F, James G, OHara J, Ong J, et al.
Biomech Model Mechanobiol
. 2019 Oct;
19(4):1319-1329.
PMID: 31571084
Sagittal craniosynostosis consists of premature fusion (ossification) of the sagittal suture during infancy, resulting in head deformity and brain growth restriction. Spring-assisted cranioplasty (SAC) entails skull incisions to free the...
5.
Knoops P, Papaioannou A, Borghi A, Breakey R, Wilson A, Jeelani O, et al.
Sci Rep
. 2019 Sep;
9(1):13597.
PMID: 31537815
Current computational tools for planning and simulation in plastic and reconstructive surgery lack sufficient precision and are time-consuming, thus resulting in limited adoption. Although computer-assisted surgical planning systems help to...
6.
OHara J, Ruggiero F, Wilson L, James G, Glass G, Jeelani O, et al.
Mol Syndromol
. 2019 Apr;
10(1-2):83-97.
PMID: 30976282
Patients with syndromic craniosynostosis have a molecularly identified genetic cause for the premature closure of their cranial sutures and associated facial and extra-cranial features. Their clinical complexity demands comprehensive management...
7.
Stagliano S, DArco F, Tan A, Jeelani O, Morana G, Mankad K
Quant Imaging Med Surg
. 2018 Dec;
8(9):971-978.
PMID: 30505725
No abstract available.
8.
Knoops P, Borghi A, Ruggiero F, Badiali G, Bianchi A, Marchetti C, et al.
PLoS One
. 2018 May;
13(5):e0197209.
PMID: 29742139
Repositioning of the maxilla in orthognathic surgery is carried out for functional and aesthetic purposes. Pre-surgical planning tools can predict 3D facial appearance by computing the response of the soft...
9.
Toescu S, James G, Phipps K, Jeelani O, Thompson D, Hayward R, et al.
Neurosurgery
. 2018 Apr;
84(3):636-646.
PMID: 29617945
Background: Brain tumors in the first year of life are rare and their management remains challenging. Objective: To report on the contemporary management of brain tumors in infants with reference...
10.
Glass G, Ruff C, Crombag G, Verdoorn M, Koudstaal M, Anguilla F, et al.
Plast Reconstr Surg
. 2018 Feb;
141(3):747-750.
PMID: 29481405
Apert syndrome is characterized by hypertelorism, a negative canthal axis, and central midfacial hypoplasia, resulting in a biconcave face. Bipartition distraction partially corrects these facial anomalies. This study investigates limitations...