Syringomyelia
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Subject Areas on Research
- A genetic hypothesis for Chiari I malformation with or without syringomyelia.
- Atypical hemifacial microsomia associated with Chiari I malformation and syrinx: further evidence indicating that chiari I malformation is a disorder of the paraaxial mesoderm. Case report and review of the literature.
- Basilar invagination.
- Chiari malformation Type I surgery in pediatric patients. Part 2: complications and the influence of comorbid disease in California, Florida, and New York.
- Chiari malformation clusters describe differing presence of concurrent anomalies based on Chiari type.
- Clinical, radiological, and genetic similarities between patients with Chiari Type I and Type 0 malformations.
- Development of an acquired Chiari malformation Type I in the setting of an untreated lipomyelomeningocele. Case report.
- Dorsal thoracic arachnoid web and the "scalpel sign": a distinct clinical-radiologic entity.
- Exophytic syrinx, an extreme form of syringomyelia: CT, myelographic, and MR imaging features.
- Isolated Horner syndrome and syringomyelia in a child.
- Morphometric Analysis of Predictors of Cervical Syrinx Formation in the Setting of Chiari I Malformation.
- Patients with Chiari malformation Type I presenting with acute neurological deficits: case series.
- Relationship of cine phase-contrast magnetic resonance imaging with outcome after decompression for Chiari I malformations.
- Resolution of syringohydromyelia with targeted CT-guided epidural blood patching.
- Surgical Correction of an Extensive Skull Base Defect as a Result of Pneumocele.
- Syringomyelia in a man with sarcoidosis.