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期刊名:Orbit-the international journal on orbital disorders-oculoplastic and lacrimal surgery

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ISSN:0167-6830

e-ISSN:1744-5108

IF/分区:0.9/N/A

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共收录本刊相关文章索引2243
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Delia D Wang,Timothy J Sullivan Delia D Wang
Purpose: This study presents the clinical features and management of paediatric TED patients in an Australian population, together with the longitudinal trend of TRAb and TSI over time. ...
Viana N Phan,Emma C McDonnell,Laura T Phan et al. Viana N Phan et al.
Purpose: To present a modified evisceration technique with a full-thickness horizontal sclerotomy and assess post-operative motility and long-term outcomes. ...
K Farde,F Träisk K Farde
Purpose: To analyze Tocilizumab (TCZ, an interleukin 6 inhibitor) as a second-line treatment for thyroid-associated ophthalmopathy (TAO). Methods: ...
Paulina Truong,Saif Aldeen Alryalat,Osama Al Deyabat et al. Paulina Truong et al.
Pleomorphic adenoma of the lacrimal gland (PALG) is a benign neoplasm typically presenting with gradual, painless globe displacement and/or lid swelling. We report an atypical case of PALG in a 53-year old male presenting acutely, mimicking...
Marissa K Shoji,Benjamin I Meyer,Nina Diklich et al. Marissa K Shoji et al.
Introduction: Rhabdomyosarcoma (RMS) is a common pediatric orbital malignancy but is extremely rare in adults. This study assesses clinical and radiographic features, management, and outcomes in adult orbital RMS patients...
Hidetaka Miyazaki,Jonnah Kristina Teope,Yasuhiro Takahashi et al. Hidetaka Miyazaki et al.
Purpose: To describe a technique using retroauricular scalp graft for eyebrow reconstruction, along with problems encountered and countermeasures in treatment. ...
Tatiana Boza,Doris Quiroz,Mariana Nadais Aidar et al. Tatiana Boza et al.
Ablepharon macrostomia syndrome is a rare congenital disorder caused by autosomal-dominant TWIST2 mutations. This condition is characterized by redundant skin, low-set ears, macrostomia, ambiguous genitalia, and underdevelopment of the both...