Severe myoclonic epilepsy of infancy (Dravet syndrome): Recognition and diagnosis in adults-Reference-Cited by-同舟云学术

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Severe myoclonic epilepsy of infancy (Dravet syndrome): Recognition and diagnosis in adults

Published:2006-12-26 Issue:12 Volume:67 Page:2224-2226
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Jansen F. E.,Sadleir L. G.,Harkin L. A.,Vadlamudi L.,McMahon J. M.,Mulley J. C.,Scheffer I. E.,Berkovic S. F.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 142 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. Practical considerations for the use of fenfluramine to manage patients with Dravet syndrome or Lennox–Gastaut syndrome in clinical practice;Epilepsia Open;2024-07-04

2. The efficacy and safety of cannabidiol (CBD) in pediatric patients with Dravet Syndrome: a narrative review of clinical trials;European Journal of Medical Research;2024-03-18

3. Epilepsies;Handbook of Clinical Neurology;2024

4. Clinical and Genetic Features of Dravet Syndrome: A Prime Example of the Role of Precision Medicine in Genetic Epilepsy;International Journal of Molecular Sciences;2023-12-19

5. GABA_A receptors in epilepsy: Elucidating phenotypic divergence through functional analysis of genetic variants;Journal of Neurochemistry;2023-08-24

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