KCNQ2encephalopathy-Reference-Cited by-同舟云学术

KCNQ2encephalopathy

Published:2016-08-22 Issue:5 Volume:2 Page:e96
ISSN:2376-7839
Container-title:Neurology Genetics
language:en
Short-container-title:Neurol Genet

Author:

Millichap John J.,Park Kristen L.,Tsuchida Tammy,Ben-Zeev Bruria,Carmant Lionel,Flamini Robert,Joshi Nishtha,Levisohn Paul M.,Marsh Eric,Nangia Srishti,Narayanan Vinodh,Ortiz-Gonzalez Xilma R.,Patterson Marc C.,Pearl Phillip L.,Porter Brenda,Ramsey Keri,McGinnis Emily L.,Taglialatela Maurizio,Tracy Molly,Tran Baouyen,Venkatesan Charu,Weckhuysen Sarah,Cooper Edward C.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics(clinical),Clinical Neurology

Reference39 articles.

1. A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation

2. Neonatal convulsions and epileptic encephalopathy in an Italian family with a missense mutation in the fifth transmembrane region of KCNQ2

3. Neonatal seizures with tonic clonic sequences and poor developmental outcome

4. Benign familial neonatal convulsions: Always benign?

5. KCNQ2 encephalopathy: Emerging phenotype of a neonatal epileptic encephalopathy

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3. Plural molecular and cellular mechanisms of pore domain KCNQ2 encephalopathy;2024-08-27

4. Donepezil as a new therapeutic potential in KCNQ2- and KCNQ3-related autism;Frontiers in Cellular Neuroscience;2024-08-08

5. Clinical and genetic analysis of 18 patients with <i>KCNQ2 </i>mutations from South China;The Turkish Journal of Pediatrics;2024-05-23