Publications by authors named "Arianne J Boylan"

Study Design: Systemic review.

Objective: To understand the role of cervical disk arthroplasty in the treatment of cervical myelopathy.

Summary Of Background Data: The surgical management of degenerative cervical myelopathy (DCM) most frequently involves decompression and fusion, but stiffness introduced by the fusion and adjacent segment degeneration remain problems that can result in significant morbidity.

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Objective: To compare the perioperative morbidity of 2-level anterior cervical discectomy and fusion (ACDF) with that of 1-level anterior cervical corpectomy and fusion (ACCF) for the treatment of cervical degenerative conditions.

Methods: A retrospective study of the 2005-2016 National Surgical Quality Improvement Program database for patients undergoing 2-level ACDF and 1-level ACCF was performed. Patient data included: age, sex, body mass index (BMI), functional status, and American Society of Anesthesiologists (ASA) physical status (PS) classification.

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Introduction: The most commonly used classification system for caudal appendages (aka human tails) dates from the 1980s and classifies appendages (tails) as either true tails or pseudotails. Advances in neuroimaging since the 1980s, however, as well as an ever-increasing number of reported cases, have made this system outdated. Sacrococcygeal eversion is a condition in which the distal sacral and coccygeal vertebrae are curved in a retroverted rather than anteverted direction.

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Cerebellar tonsils moved significantly upward in 3 patients with Chiari type I who underwent supratentorial cranial vault expansion to alleviate intracranial pressure related to multisutural craniosynostosis. The Chiari type I deformities in these patients were the biomechanical consequence of posterior fossa-cerebellar disproportion caused by supratentorial craniocerebral disproportion secondary to multisutural craniosynostosis. The authors postulate that all cases of Chiari type I deformity share the sine qua non feature of posterior fossa-cerebellar disproportion.

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Article Synopsis
  • Mutations in PDCD10 lead to familial cerebral cavernous malformation 3 (CCM3), with a lack of understanding about its role in disease progression.
  • Researchers used in situ hybridization and immunohistochemistry to study the expression of CCM3 mRNA and protein in mouse and human tissues.
  • Findings revealed CCM3 is widely expressed in various brain regions and other organs, particularly in the neurovascular unit and arterial endothelium, indicating its potential significance in the development and progression of lesions associated with CCM3.
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