Diagnostic algorithm for children presenting with epilepsia partialis continua-Reference-Cited by-同舟云学术

Diagnostic algorithm for children presenting with epilepsia partialis continua

Published:2020-09-02 Issue:10 Volume:61 Page:2224-2233
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:Epilepsia

Author:

Surana Snehal¹,Rossor Thomas¹,Hassell Jane¹,Boyd Stewart²,D'Arco Felice³^ORCID,Aylett Sarah¹,Bhate Sanjay¹,Carr Lucinda¹,Das Krishna¹,DeVile Catherine¹,Eltze Christin¹,Hemingway Cheryl¹⁴,Kaliakatsos Marios¹,O'Callaghan Finbar¹⁵,Prabhakar Prab¹,Robinson Robert¹,Varadkar Sophia¹,Helen Cross J¹⁵,Hacohen Yael¹⁴^ORCID

Affiliation:

1. Department of Paediatric Neurology Great Ormond Street Hospital for Children London UK

2. Department of Neurophysiology Great Ormond Street Hospital for Children London UK

3. Department of Neuroradiology Great Ormond Street Hospital for Children London UK

4. Department of Neuroinflammation Queen Square MS CentreUCL Institute of Neurology London UK

5. Developmental of Neuroscience Institute of Child Health UCL London UK

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/epi.16650

Reference19 articles.

1. Epilepsia partialis continua: semiology and differential diagnoses;Bien CG;Epileptic Disord,2008

2. Clinical course and variability of non-Rasmussen, nonstroke motor and sensory epilepsia partialis continua: A European survey and analysis of 65 cases

3. Etiology, clinical features and outcome of epilepsia partialis continua in cohort of 51 children

4. Understanding the Epilepsy in POLG Related Disease

5. Status epilepticus in children with Alpers’ disease caused byPOLG1mutations: EEG and MRI features

Cited by 5 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. Red Flags in Primary Mitochondrial Diseases: What Should We Recognize?;International Journal of Molecular Sciences;2023-11-25

2. Epilepsia Partialis Continua that Improved in a Pediatric Patient with Sub-dural Empyema;Child Neurology Open;2023-01

3. Broadening the Spectrum of SLC22A5 Phenotype: Primary Carnitine Deficiency Presenting with Focal Myoclonus;Child Neurology Open;2023-01

4. Pediatric anti-NMDA receptor encephalitis with epilepsia partialis continua;Neuroimmunology Reports;2022

5. Epilepsy in Mitochondrial Diseases—Current State of Knowledge on Aetiology and Treatment;Children;2021-06-22