Infantile Epilepsy With Multifocal Myoclonus Caused by TBC1D24 Mutations

Seizure : the journal of the British Epilepsy Association - United Kingdom
doi 10.1016/j.seizure.2019.05.010
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Elsevier BV

Related search

TBC1D24, an ARF6-Interacting Protein, Is Mutated in Familial Infantile Myoclonic Epilepsy

American Journal of Human Genetics
Genetics
2010English

Progressive Myoclonus Epilepsy Caused by a Gain-Of-Function KCNA2 Mutation

Seizure : the journal of the British Epilepsy Association
MedicineNeurology
2019English

Multifocal Infantile Hemangioma

Journal of Pediatrics
Child HealthPediatricsPerinatology
2019English

Benign Familial Infantile Epilepsy

2020English

Myoclonus Epilepsy With Cerebellar Lafora Bodies: Report of a Case

Journal of Neurology, Neurosurgery and Psychiatry
PsychiatryMental HealthNeurologySurgery
1976English

An Autopsy Case of Myoclonus Epilepsy

Kurume Medical Journal
Medicine
1973English

Progressive Myoclonus Epilepsy Responded to Vagus Nerve Stimulation

SAJ Case Reports
2017English

Novel TBC1D24 Mutations in a Case of Nonconvulsive Status Epilepticus

Frontiers in Neurology
Neurology
2018English

Infantile Enteritis in Dublin Caused by Escherichia Coli O142

Journal of Medical Microbiology
MedicineMicrobiology
1973English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2025 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy