Colin Perumal,Michael Bouckaert,Martin Robson
Colin Perumal
COMPLEX, OPEN MAXILLOFACIAL FRACTURES ARE OFTEN ACCOMPANIED BY EXTENSIVE CONTAMINATION, CRUSH, OR AVULSION OF THE OVERLYING SOFT TISSUE, THERE HAVE BEEN TWO ALTERNATIVES TO TREATMENT: either radical debridement of all contaminated tissue, f...
Scopelliti Domenico,Cipriani Orlando,Fatone Flavia Maria Graziana et al.
Scopelliti Domenico et al.
Williams-Beuren syndrome (WBS) is a genomic neurodevelopmental disorder, estimated to occur in approximately 1 in 10,000 persons. It is caused by a deletion of the "elastin" gene on chromosome 7q11.23 and was described officially in 1961 by...
Bhuvana Krishnamoorthy,Ns Mamatha,Vinod Ar Kumar
Bhuvana Krishnamoorthy
Radiographic examination forms an integral component of the clinical assessment routine in patients with temporomandibular joint disorders (TMJ). There are several imaging modalities to visualize the TMJ. Cone beam computed tomography (CBCT...
Rinku K George,Arvind Krishnamurthy
Rinku K George
Reconstructive microsurgery for oral and maxillofacial (OMF) defects is considered as a niche specialty and is performed regularly only in a handful of centers. Till recently the pectoralis major myocutaneous flap (PMMC) was considered to b...
Suresh Menon,Srihari Venkatswamy,Veena Ramu et al.
Suresh Menon et al.
Objective: To highlight the clinical and radiologic features and management of craniofacial fibrous dysplasia with review of literature. Materials and met...
Ghali E Ghali,George Zakhary
Ghali E Ghali
Introduction: The past two decades have seen advances relative to the treatment of patients with craniosynostosis in the areas of resorbable fixation, imaging, and both intraoperative and perioperative management. The pur...
Gene p63: In ectrodactyly-ectodermal dysplasia clefting, ankyloblepharon-ectodermal dysplasia, Rapp-Hodgkin syndrome [0.03%]
基因p63与外胚叶发育不全-指（趾）间缺如综合征、先天性闭锁性白内障、Rapp-Hodgkin综合征的关系研究
Cornelia van Straten,Kurt-W Butow
Cornelia van Straten
Introduction: An analysis was made of three different syndromes associated with p63 gene mutations, known as ectrodactyly-ectodermal dysplasia-clefting syndrome (EEC), ankyloblepharon-ectodermal dysplasia clefting syndrom...
Immunohistochemical profiling of Ameloblastomas using cytokeratin, vimentin, smooth muscle actin, CD34 and S100 [0.03%]
用细胞角蛋白、波形蛋白、平滑肌动蛋白、CD34和S100免疫组化对成釉细胞瘤进行组织芯片构建及分析
Herald J Sherlin,Anuja Natesan,Priya Ram et al.
Herald J Sherlin et al.
Background: Ameloblastoma is characterized as a slow growing, non-metastatic and a locally invasive tumor with a high risk of recurrence. Immunohistochemical evaluation of ameloblastomas using epithelial and connective ti...
Gui-Youn Cho-Lee,Eloy-Miguel García-Díez,Richard-Agostinho Nunes et al.
Gui-Youn Cho-Lee et al.
Introduction: The alveolar cleft is a bony defect that is present in 75% of the patients with cleft lip and palate. Although secondary alveolar cleft repair is commonly accepted for these patients, nowadays, controversy s...
S M Balaji
S M Balaji
Background: Residual diplopia (RD) is the main post-treatment complication of orbital bone fracture (OBF) reduction. The cause of RD is varied and often related to the degree of inflammation, surgical timing, graft requir...