The expanding spectrum of movement disorders in genetic epilepsies-Reference-Cited by-同舟云学术

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The expanding spectrum of movement disorders in genetic epilepsies

Published:2019-11-29 Issue:2 Volume:62 Page:178-191
ISSN:0012-1622
Container-title:Developmental Medicine & Child Neurology
language:en
Short-container-title:Dev Med Child Neurol

Author:

Papandreou Apostolos¹²^ORCID,Danti Federica Rachele¹³,Spaull Robert⁴⁵^ORCID,Leuzzi Vincenzo³^ORCID,Mctague Amy¹²^ORCID,Kurian Manju A¹²^ORCID

Affiliation:

1. Molecular Neurosciences Developmental Neurosciences Programme UCL Great Ormond Street Institute of Child Health LondonUK

2. Department of Neurology Great Ormond Street Hospital London UK

3. Department of Human Neuroscience Unit of Child Neurology and Psychiatry Sapienza University of Rome Rome Italy

4. Department of Paediatric Neurology Bristol Royal Hospital for Children BristolUK

5. Bristol Medical School University of Bristol Bristol UK

Publisher

Wiley

Subject

Neurology (clinical),Developmental Neuroscience,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/dmcn.14407

Reference183 articles.

1. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology

2. The genetic landscape of the epileptic encephalopathies of infancy and childhood

3. Definition and classification of hyperkinetic movements in childhood

4. Revised terminology and concepts for organization of seizures and epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005-2009

5. Epilepsy in Rett syndrome, andCDKL5- andFOXG1-gene-related encephalopathies

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4. Channelopathies in epilepsy: an overview of clinical presentations, pathogenic mechanisms, and therapeutic insights;Journal of Neurology;2024-04-12

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