Results 21 to 30 of about 10,268 (160)

Single-cell transcriptomics reveals ependymal subtypes related to cytoskeleton dynamics as the core driver of syringomyelia pathological development

open access: yesiScience, 2023
Summary: Syringomyelia is a common clinical lesion associated with cerebrospinal fluid flow abnormalities. By a reversible model with chronic extradural compression to mimic human canalicular syringomyelia, we explored the spatiotemporal pathological ...
Chunli Lu   +6 more
doaj   +1 more source

Chronic extradural compression of spinal cord leads to syringomyelia in rat model

open access: yesFluids and Barriers of the CNS, 2020
Background Syringomyelia is a common spinal cord lesion. However, whether CSF blockage is linked to the formation and enlargement of syringomyelia is still controversial.
Longbing Ma   +5 more
doaj   +1 more source

Spinal Obstruction-Related vs. Craniocervical Junction-Related Syringomyelia: A Comparative Study

open access: yesFrontiers in Neurology, 2022
BackgroundNo prior reports have focused on spinal cord injury (SCI) characteristics or inflammation after destruction of the blood–spinal cord barrier by syringomyelia.
Chenghua Yuan   +79 more
doaj   +1 more source

Intradural Extramedullary Epidermoid Cyst at the Conus Medullaris Level with Thoracic Syringomyelia: a Case Report

open access: yesActa Medica, 2019
Spinal epidermoid cysts are benign tumors. Syringomyelia secondary to intramedullary tumors are frequently observed. However, the association between syringomyelia and spinal intradural extramedullary epidermoid cyst in the conus medullaris region is ...
Bekir Akgun   +3 more
doaj   +1 more source

Progressive Scoliosis and Syringomyelia - Questions of Surgical Approach

open access: yesFolia Medica, 2018
Background: The rate of scoliosis in syringomyelia patients ranges from 25 to 74.4%. In turn, syringomyelia occurs in 1.2% to 9.7% of scoliosis patients.
Mikhaylovskiy Mikhail   +18 more
doaj   +1 more source

Decoding Chiari Malformation and Syringomyelia: From Epidemiology and Genetics to Advanced Diagnosis and Management Strategies

open access: yesBrain Sciences, 2023
Chiari Malformation and Syringomyelia are neurosurgical entities that have been the subject of extensive research and clinical interest. Globally prevalent, these disorders vary demographically and have witnessed evolving temporal trends.
Corneliu Toader   +7 more
doaj   +1 more source

Selective thoracolumbar/lumbar fusion for Syringomyelia-associated scoliosis: a case-control study with Lenke 5C adolescent idiopathic scoliosis

open access: yesBMC Musculoskeletal Disorders, 2020
Background Selective thoracolumbar/lumbar fusion technique was introduced to treat adolescent idiopathic scoliosis (AIS) patients with major thoracolumbar/lumbar curves.
Fan Feng   +6 more
doaj   +1 more source

Multiple sclerosis and syringomyelia – a case report

open access: yesAktualności Neurologiczne, 2019
Syringomyelia is associated with more than two-thirds of Chiari malformation type I cases, and rarely with intramedullary neoplasm or post-traumatic cavitations.
Katarzyna Kapica-Topczewska   +5 more
doaj   +1 more source

Surgical outcomes of posterior correction surgery for scoliosis associated with syringomyelia

open access: yesInterdisciplinary Neurosurgery, 2022
Objective: Although syringomyelia is considered a risk factor for neurological complications of correction surgery for scoliosis, only a few reports on the surgical results of the correction surgery complicated with associated syringomyelia are available.
Osahiko Tsuji   +10 more
doaj   +1 more source

Risk factors for the presence of syringomyelia in idiopathic scoliosis: analysis of 3,285 cases and brief literature review

open access: yesХирургия позвоночника, 2020
Objective. To analyze possible radiological and clinical risk factors for syringomyelia in patients with scoliotic deformity. Material and Methods. An analysis of data from 3,285 patients with idiopathic scoliosis treated from 1997 to 2020 was performed.
Vadim V. Belozerov   +1 more
doaj   +1 more source

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