Natural history of Chiari I malformation with syrinx and dilatation of the central canal in the pediatric population: the CHEO experience
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Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s00381-023-06273-9.pdf
Reference20 articles.
1. Van Der Veken J, Harding M, Hatami S, Agzarian M, Vrodos N (2021) Syringomyelia intermittens: highlighting the complex pathophysiology of syringomyelia. Illustrative case. J Neurosurg Case lessons 2:CASE21341. https://doi.org/10.3171/CASE21341
2. Szuflita NS, Phan TN, Boulter JH, Keating RF, Myseros JS (2021) Nonoperative management of enlarging syringomyelia in clinically stable patients after decompression of Chiari malformation type I. J Neurosurg Pediatr. https://doi.org/10.3171/2020.12.PEDS20621
3. Strahle J, Muraszko KM, Kapurch J, Bapuraj JR, Garton HJL, Maher CO (2011) Natural history of Chiari malformation Type I following decision for conservative treatment. J Neurosurg Pediatr 8:214–221. https://doi.org/10.3171/2011.5.PEDS1122
4. Schuster JM, Zhang F, Norvell DC, Hermsmeyer JT (2013) Persistent/Recurrent syringomyelia after Chiari decompression-natural history and management strategies: a systematic review. Evid Based Spine Care J 4:116–125. https://doi.org/10.1055/s-0033-1357362
5. Avellino AM, Kim DK, Weinberger E, Roberts TS (1996) Resolution of spinal syringes and Chiari I malformation in a child Case illustration
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