A genetic component in Chiari I malformation: Chiari 1 malformation in all five family members-Reference-Cited by-同舟云学术

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A genetic component in Chiari I malformation: Chiari 1 malformation in all five family members

Published:2024-04 Issue:4 Volume:19 Page:1445-1451
ISSN:1930-0433
Container-title:Radiology Case Reports
language:en
Short-container-title:Radiology Case Reports

Author:

Hassan Taha F.,Morgan Ryan D.^ORCID,Psaromatis Kirie M.^ORCID,Baronia Benedicto C.

Publisher

Elsevier BV

Reference22 articles.

1. Cerebellar tonsil ectopia measurement in type I Chiari malformation patients show poor inter-operator reliability;Lawrence;Fluids Barriers CNS,2018

2. Chiari type I malformation, syncope, headache, hypoglycemia and hepatic steatosis in an 8-year old girl: a causal association?;Tarani;Pediatr Rep,2010

3. Spontaneous resolution of aberrant cerebellar tonsil movement in a patient with improving Chiari I malformation;Morgan;Radiol Case Rep,2022

4. Association of cerebellar tonsil dynamic motion and outcomes in pediatric Chiari I malformation;Collins;World Neurosurg,2022

5. Cerebellar and hindbrain motion in Chiari malformation with and without syringomyelia;Leung;J Neurosurg Spine,2016

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