Results 41 to 50 of about 2,682 (177)
Periodontology 2000, EarlyView.Abstract Objectives Global population aging is leading to a greater retention of natural teeth into later life and an increasing prevalence of dental implant therapy. Although advanced age has traditionally been regarded as a risk factor for compromised outcomes, population level evidence remains lacking.
Dong Yang +3 more
wiley +1 more source
Interdisciplinary Neurosurgery, 2018 Background: Anterior odontoid screw fixation for the treatment of type II odontoid fractures, in contrast to posterior C1–2 fusion, allows for maintenance of cervical rotatory motion at C1–2. The approach requires an accessible C2–3 disc space from which
Sohail H. Syed, M.D. +4 more
doaj +1 more source
Endoscopic‐Assisted Posterior Atlantoaxial Fusion: Technical Innovation and Clinical Experience
Orthopaedic Surgery, Volume 18, Issue 8, Page 1768-1782, August 2026.Endoscopic‐assisted posterior atlantoaxial lateral mass fusion is introduced as a novel minimally invasive technique for treating atlantoaxial instability. The approach enables direct visualization, precise fixation, and effective bone fusion while minimizing muscle dissection, blood loss, and postoperative pain, achieving rapid neurological and ...
Jichong Zhu +7 more
wiley +1 more source
대한영상의학회지, 2017 Traumatic posterior atlantoaxial dislocation without odontoid fracture is very rare. Patient prognosis depends on the neurologic symptoms or the extent of damage to the structures.
Yong Kyun Kim +4 more
doaj +1 more source
Odontoid synchondrosis fractures in children [PDF]
Neurosurgical Focus, 2006 Object Odontoid synchondrosis fractures, although rare in the overall incidence of spinal trauma, are one of the more common fractures in young children. The goal of this study was to evaluate the demographic data, incidence of neurological deficits, treatment strategies, and outcomes in a combined series of ...
Daniel R, Fassett +2 more
openaire +2 more sources
Teriparatide in Two Patients With Mucopolysaccharidosis Type IVB
JIMD Reports, Volume 67, Issue 3, May 2026.ABSTRACT Mucopolysaccharidosis Type IV is a multisystem lysosomal storage disease characterized by severe skeletal dysplasia resulting from impaired degradation of the glycosaminoglycans keratan sulfate and chondroitin‐6‐sulfate. The condition is classified into Types A and B based on the underlying enzyme deficiency.
Mark Wijnen +5 more
wiley +1 more source
Risk factors of fracture stability and osseous union of Type II odontoid fractures
Interdisciplinary NeurosurgeryPurpose: To evaluate fracture stability rates after conservative treatment and osseous union rates after surgery in patients with Type II odontoid fractures, and to identify clinical and radiologic risk factors associated with these outcomes.
Doohee Han +3 more
doaj +1 more source
Ischiopubic and odontoid synchondrosis in a boy with progressive pseudorheumatoid chondrodysplasia
Pediatric Rheumatology Online Journal, 2007 Purpose To present the case of a 14-year-old boy with clinical and radiographic features of pseudorheumatoid chondrodyspalsia with additional, potentially serious, cervical malformations.
Ben Ghachem Maher +4 more
doaj +1 more source
Management of odontoid fractures in the elderly [PDF]
European Spine Journal, 1999 Odontoid fractures are frequent in patients over 70 years of age, and in patients over 80 years of age they form the majority of spinal fractures. In a retrospective analysis of 23 geriatric (> 70 years) patients with a fracture of the odontoid, we compared some of the clinical features to a contemporary series of patients younger than 70 years of age.
E J, Müller, M, Wick, O, Russe, G, Muhr
openaire +2 more sources
Saul Wilson Syndrome: A Case Report With New Features in Saudi Arabia
Clinical Case Reports, Volume 14, Issue 2, February 2026.ABSTRACT Saul Wilson syndrome is an extremely rare genetic disorder caused by heterozygous de novo mutations in the COG4 gene. We report the first case from Saudi Arabia with previously unreported facial dysmorphic features, expanding the known phenotypic spectrum and emphasizing the importance of recognizing phenotypic variability in rare disorders.
Saad A. Bin Owaimer +4 more
wiley +1 more source