De novo absence status epilepticus associated with the <scp><i>SLC6A1</i></scp> gene in a pediatric patient-Reference-Cited by-同舟云学术

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De novo absence status epilepticus associated with the SLC6A1 gene in a pediatric patient

Published:2023-11-06 Issue: Volume: Page:
ISSN:1294-9361
Container-title:Epileptic Disorders
language:en
Short-container-title:Epileptic Disorders

Author:

Caraballo Roberto H.¹^ORCID,Chacón Santiago²,Touzon Maria Sol¹,Loos Mariana¹,Juanes Matías¹

Affiliation:

1. Hospital de Pediatría “Prof. Dr. Juan P Garrahan” Buenos Aires Argentina

2. Hospital Regional de Gualeguaychú Gualeguaychú Argentina

Publisher

Wiley

Subject

Neurology (clinical),Neurology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/epd2.20175

Reference10 articles.

1. De novo absence status epilepticus in three paediatric patients: a new idiopathic epilepsy syndrome?

2. De novo Absence Status Epilepticus in a pediatric cohort: Electroclinical pattern in a multicenter Italian patients cohort

3. Mutations in the GABA Transporter SLC6A1 Cause Epilepsy with Myoclonic-Atonic Seizures

4. Current knowledge of SLC6A1-related neurodevelopmental disorders

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A transporter’s doom or destiny: SLC6A1 in health and disease, novel molecular targets and emerging therapeutic prospects;Frontiers in Molecular Neuroscience;2024-08-29

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