Autosomal dominant lateral temporal lobe epilepsy associated with a novel reelin mutation-Reference-Cited by-同舟云学术

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Autosomal dominant lateral temporal lobe epilepsy associated with a novel reelin mutation

Published:2020-08 Issue:4 Volume:22 Page:443-448
ISSN:1294-9361
Container-title:Epileptic Disorders
language:
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Author:

Michelucci Roberto,Dazzo Emanuela,Volpi Lilia,Pasini Elena,Riguzzi Patrizia,Minardi Raffaella,Marliani Anna Federica,Tappatà Maria,Bisulli Francesca,Tassinari Carlo Alberto,Nobile Carlo

Publisher

John Libbey Eurotext

Subject

Clinical Neurology,Neurology,General Medicine

Cited by 9 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. De novo monoallelic Reelin missense variants cause dominant neuronal migration disorders via a dominant-negative mechanism;Journal of Clinical Investigation;2024-07-09

2. Inhibition of Granule Cell Dispersion and Seizure Development by Astrocyte Elevated Gene-1 in a Mouse Model of Temporal Lobe Epilepsy;Biomolecules;2024-03-20

3. Heterozygous RELN missense variants associated with genetic generalized epilepsy;Seizure: European Journal of Epilepsy;2023-10

4. Inhibition of granule cell dispersion and seizure development by AAV1-AEG-1 administration in a mouse model of TLE;2023-08-21

5. Monoallelic and biallelic mutations in RELN underlie a graded series of neurodevelopmental disorders;Brain;2022-06-30

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