Clinical, radiological, and genetic similarities between patients with Chiari Type I and Type 0 malformations. - Wikidata - awgldk - TriplyDB

Clinical, radiological, and genetic similarities between patients with Chiari Type I and Type 0 malformations.

Clinical, radiological, and genetic similarities between patients with Chiari Type I and Type 0 malformations.

http://www.wikidata.org/entity/Q36919575

about

Genetic evaluation and application of posterior cranial fossa traits as endophenotypes for Chiari type I malformation Stratified whole genome linkage analysis of Chiari type I malformation implicates known Klippel-Feil syndrome genes as putative disease candidates.Quantitative analysis of Chiari-like malformation and syringomyelia in the Griffon Bruxellois dog.Pseudomeningocele formation following chiari decompression: 19-year retrospective review of predisposing and prognostic factors Treatment of Syringomyelia due to Chiari Type I Malformation with Syringo-Subarachnoid-Peritoneal Shunt.Traumatic Transient Herniation Concomitant with Tonsillar Hemorrhagic Contusion in a Child.Comparison of the scoliosis curve patterns and MRI syrinx cord characteristics of idiopathic syringomyelia versus Chiari I malformation.The human foramen magnum--normal anatomy of the cisterna magna in adults.Concurrent paediatric medulloblastoma and Chiari I malformation with syringomyelia.

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P2860

Clinical, radiological, and genetic similarities between patients with Chiari Type I and Type 0 malformations.

http://www.wikidata.org/entity/Q36919575

description

2012 nî lūn-bûn

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2011.12.PEDS11113

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Journal of neurosurgery. Pediatrics

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Clinical, radiological, and ge ...... ype I and Type 0 malformations

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Bermans J Iskandar

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Marcy C Speer

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R Shane Tubbs

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Roham Moftakhar

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Simon G Gregory

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W Jerry Oakes

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P2860

Syndrome of occipitoatlantoaxial hypermobility, cranial settling, and Chiari malformation Type I in patients with hereditary disorders of connective tissue

Dimensions of the posterior fossa in patients symptomatic for Chiari I malformation but without cerebellar tonsillar descent

Mechanisms of cerebellar tonsil herniation in patients with Chiari malformations as guide to clinical management.

Syringomyelia without hindbrain herniation: tight cisterna magna. Report of four cases and a review of the literature.

Pediatric Chiari malformation Type 0: a 12-year institutional experience.

Clinical and neuroimaging features of "idiopathic" syringomyelia.

Familial syringomyelia: the first Japanese case and review of the literature.

Chiari in the family: inheritance of the Chiari I malformation.

Review Article: Chiari Type I Malformation with or Without Syringomyelia: Prevalence and Genetics.

Evidence of posterior fossa hypoplasia in the familial variant of adult Chiari I malformation: case report.

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372-378

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Allison Ashley-Koch

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22462700

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