Cavitating Leukoencephalopathy in a Child Carrying the MitochondrialA8344GMutation: Fig 1.-Reference-Cited by-同舟云学术

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Cavitating Leukoencephalopathy in a Child Carrying the MitochondrialA8344GMutation: Fig 1.

Published:2010-06-25 Issue:9 Volume:31 Page:E78-E79
ISSN:0195-6108
Container-title:American Journal of Neuroradiology
language:en
Short-container-title:AJNR Am J Neuroradiol

Author:

Biancheri R.,Rossi D.,Cassandrini D.,Rossi A.,Bruno C.,Santorelli F.M.

Publisher

American Society of Neuroradiology (ASNR)

Subject

Clinical Neurology,Radiology Nuclear Medicine and imaging

Reference4 articles.

1. Invited Article: An MRI-based approach to the diagnosis of white matter disorders

2. Bilateral Putaminal Necrosis Associated With the Mitochondrial DNA A8344G Myoclonus Epilepsy With Ragged Red Fibers (MERRF) Mutation: An Infantile Case

3. Severe Infantile Encephalomyopathy Caused by a Mutation in COX6B1, a Nucleus-Encoded Subunit of Cytochrome C Oxidase

4. Progressive cavitating leukoencephalopathy: A novel childhood disease

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1. Phenotyping mitochondrial DNA‐related diseases in childhood: A cohort study of 150 patients;European Journal of Neurology;2023-04-25

2. Progressive cavitating leukoencephalopathy associated with a homozygous POLG mutation of 264C>G (p.F88L);Radiology Case Reports;2020-07

3. Pharmacotherapeutic management of epilepsy in MERRF syndrome;Expert Opinion on Pharmacotherapy;2019-05-07

4. Genotypic Spectrum and Natural History of Cavitating Leukoencephalopathies in Childhood;Pediatric Neurology;2019-05

5. Mitochondrial Neurodegenerative Disorders II: Ataxia, Dystonia and Leukodystrophies;Diagnosis and Management of Mitochondrial Disorders;2019

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