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Epidemiology of Chiari I Malformation and Syringomyelia.
Neurosurgery clinics of North America, 2022Chiari I malformation is a common condition seen by adult and pediatric neurosurgeons. With increased utilization of MRI over time, incidental findings of Chiari I malformation are occurring more frequently.
Katherine G. Holste +2 more
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Veterinary Clinics of North America: Small Animal Practice, 2016
Chiari-like malformation is a condition of the craniocervical junction in which there is a mismatch of the structures of the caudal cranial fossa causing the cerebellum to herniate into the foramen magnum. This herniation can lead to fluid buildup in the spinal cord, also known as syringomyelia.
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Chiari-like malformation is a condition of the craniocervical junction in which there is a mismatch of the structures of the caudal cranial fossa causing the cerebellum to herniate into the foramen magnum. This herniation can lead to fluid buildup in the spinal cord, also known as syringomyelia.
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Archives of Neurology, 2003
Current understanding of cerebellar ectopia is primarily based on the detailed study and classification of this rare rhombencephalon deformity by Hans Chiari, MD, more than a century ago. Recent advances in neuroradiology, especially since the introduction of magnetic resonance imaging, have enabled the incidental diagnosis of cerebellar ectopia.
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Current understanding of cerebellar ectopia is primarily based on the detailed study and classification of this rare rhombencephalon deformity by Hans Chiari, MD, more than a century ago. Recent advances in neuroradiology, especially since the introduction of magnetic resonance imaging, have enabled the incidental diagnosis of cerebellar ectopia.
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The Arnold - Chiari Malformation
Spine, 1986The Arnold-Chiari malformation is a developmental abnormality of the brainstem and cerebellum with displacement of these structures into the cervical spinal canal. Other anomalies involving the base of the skull and vertebral bodies are frequently present. In children, hydrocephalus and myelomeningocele may complicate the picture.
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Chiari malformation in craniosynostosis
Child's Nervous System, 2005Chiari malformation (CM) is a frequent finding in multisutural and syndromic craniosynostosis, occurring in 70% of patients with Crouzon's syndrome, 75% with oxycephaly, 50% with Pfeiffer's syndrome and 100% with the Kleeblattschädel deformity. The pathogenesis of this condition and rationale for treatment are still controversial.Since its first ...
Giuseppe, Cinalli +7 more
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The arnold-chiari malformation
Clinical Radiology, 1974A number of patients with neurological deficits which could be localised at the level of the foramen magnum often remain undiagnosed, or are condemned to a diagnosis of a progressive incurable degenerative disease such as multiple sclerosis. It is essential in such cases to exclude some minor degree of cerebellar tonsillar protrusion as a cause.
S, Bloch, M J, Van Rensburg, J, Danziger
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Chiari Malformation in Pregnancy
Nursing for Women's Health, 2015The diagnosis of Chiari malformation is on the rise owing to the increased frequency of brain imaging for concussion and trauma. This abnormal brain physiology can have a significant impact on the care management of a pregnant woman during the gestational period.
Sheryl E, Parfitt, Cheryl K, Roth
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Journal of clinical neuroscience, 2018
Chiari malformations are structural defects in the posterior fossa where the cerebellum displaces caudally into the foramen magnum and upper spinal canal.
Samantha R Horn +7 more
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Chiari malformations are structural defects in the posterior fossa where the cerebellum displaces caudally into the foramen magnum and upper spinal canal.
Samantha R Horn +7 more
semanticscholar +1 more source
Rhombencephalosynapsis and a Chiari II Malformation
Journal of Computer Assisted Tomography, 2003Rhombencephalosynapsis is an anomaly of the hindbrain characteristically presenting with cerebellar fusion and absence of cerebellar vermis on magnetic resonance imaging. Its association with spinal anomalies has not been reported previously.
Sener, RN, Dzelzite, S
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