Review Article: Chiari Type I Malformation with or Without Syringomyelia: Prevalence and Genetics-Reference-Cited by-同舟云学术

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

Published:2003-06-09 Issue:4 Volume:12 Page:297-311
ISSN:1059-7700
Container-title:Journal of Genetic Counseling
language:en
Short-container-title:J Genet Counsel

Author:

Speer Marcy C.¹,Enterline David S.¹,Mehltretter Lorraine¹,Hammock Preston¹,Joseph Judith¹,Dickerson Margaret¹,Ellenbogen Richard G.²,Milhorat Thomas H.³,Hauser Michael A.¹,George Timothy M.¹

Affiliation:

1. ; Duke University Medical Center; Durham North Carolina

2. ; Children's Hospital; Seattle, Washington

3. The Chiari Institute; Manhasset New York

Publisher

Wiley

Subject

Genetics (clinical)

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1023948921381/fullpdf

Reference65 articles.

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2. Evidence of posterior fossa hypoplasia in the familial variant of adult Chiari I malformation: Case report;Atkinson;Neurosurgery,1998

3. Posterior fossa volume and response to suboccipital decompression in patients with Chiari 1 malformation;Badie;Neurosurgery,1995

4. Significance of cerebellar tonsillar position on MR;Barkovich;Am J Neuroradiol,1986

5. Syringomyelia associated with spinal arachnoiditis;Barnett,1973

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