Encephalopathy with Neuroserpin Inclusion Bodies Presenting as Progressive Myoclonus Epilepsy and Associated with a Novel Mutation in the Proteinase Inhibitor 12 Gene-Reference-Cited by-同舟云学术

Encephalopathy with Neuroserpin Inclusion Bodies Presenting as Progressive Myoclonus Epilepsy and Associated with a Novel Mutation in the Proteinase Inhibitor 12 Gene

Published:2011-03-24 Issue: Volume: Page:no-no
ISSN:1015-6305
Container-title:Brain Pathology
language:en
Short-container-title:

Author:

Hagen Matthew C.,Murrell Jill R.,Delisle Marie-Bernadette,Andermann Eva,Andermann Frederick,Guiot Marie Christine,Ghetti Bernardino

Publisher

Wiley

Subject

Neurology (clinical),Pathology and Forensic Medicine,General Neuroscience

Reference27 articles.

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3. Neuroserpin mutation causes electrical status epilepticus of slow-wave sleep;Coutelier;Neurology,2008

4. Familial encephalopathy with neuroserpin inclusion bodies;Davis;Am J Pathol,1999

5. Familial dementia caused by polymerization of mutant neuroserpin;Davis;Nature,1999

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1. Familial encephalopathy with neuroserpin inclusion bodies (FENIB) presenting as catatonia: A case report in a psychiatry setting;Indian Journal of Psychiatry;2024-07

2. Frontal deficits and atrophy in a patient with familial encephalopathy with neuroserpin inclusion bodies detected by single-case voxel-based morphometry: a case report;BMC Neurology;2024-01-02

3. How the endoplasmic reticulum staggers toward failure: new targets for neuroprotection;Natural Molecules in Neuroprotection and Neurotoxicity;2024

4. Frontal deficits and atrophy in a patient with neuroserpinosis detected by single-case voxel-based morphometry: A case report;2023-11-09

5. An Unusual Case of Progressive Myoclonic Epilepsy (PME): Familial Encephalopathy with Neuroserpin Inclusion Body (FENIB);Journal of Pediatric Epilepsy;2023-05-26