CDKL5 mutations in boys with severe encephalopathy and early-onset intractable epilepsy-Reference-Cited by-同舟云学术

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CDKL5 mutations in boys with severe encephalopathy and early-onset intractable epilepsy

Published:2008-09-22 Issue:13 Volume:71 Page:997-999
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Elia M.,Falco M.,Ferri R.,Spalletta A.,Bottitta M.,Calabrese G.,Carotenuto M.,Musumeci S. A.,Lo Giudice M.,Fichera M.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 93 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. Radiographic and Tomographic Study of the Cranial Bones in Children with the Idiopathic Type of West Syndrome;Pediatric Reports;2024-05-24

2. First report of Tunisian patients with CDKL5‐related encephalopathy;Epilepsia Open;2023-09-13

3. CDKL5 deficiency disorder: progressive brain atrophy may be part of the syndrome;Cerebral Cortex;2023-07-10

4. Rett Syndrome: A Tale of Altered Genetics, Synaptic Plasticity, and Neurodevelopmental Dynamics;Cureus;2023-07-08

5. Epilepsy-Related CDKL5 Deficiency Slows Synaptic Vesicle Endocytosis in Central Nerve Terminals;The Journal of Neuroscience;2023-02-09

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