Prevalence and Impact of Underlying Diagnosis and Comorbidities on Chiari 1 Malformation-Reference-Cited by-同舟云学术

Prevalence and Impact of Underlying Diagnosis and Comorbidities on Chiari 1 Malformation

Published:2020-05 Issue: Volume:106 Page:32-37
ISSN:0887-8994
Container-title:Pediatric Neurology
language:en
Short-container-title:Pediatric Neurology

Author:

Sadler Brooke^ORCID,Kuensting Timothy,Strahle Jennifer,Park Tae Sung,Smyth Matthew,Limbrick David D.,Dobbs Matthew B.,Haller Gabe,Gurnett Christina A.

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,Neurology,Pediatrics, Perinatology, and Child Health

Reference24 articles.

1. Review article: Chiari type I malformation with or without syringomyelia: prevalence and genetics;Speer;J Genet Couns,2003

2. Stratified whole genome linkage analysis of Chiari type I malformation implicates known Klippel-Feil syndrome genes as putative disease candidates;Markunas;PLoS One,2013

3. Chiari malformation Type I and syrinx in children undergoing magnetic resonance imaging;Strahle;J Neurosurg Pediatr,2011

4. Chiari malformation type I: a case-control association study of 58 developmental genes;Urbizu;PLoS One,2013

5. Spinal deformity associated with Chiari malformation;Kelly;Neurosurg Clin N Am,2015

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