Kessi M - Search Results

1

Intellectual Disability and Potassium Channelopathies: A Systematic Review.

Kessi M, Chen B, Peng J, Tang Y, Olatoutou E, He F, Yang L, Yin F. Kessi M, et al. Front Genet. 2020 Jun 23;11:614. doi: 10.3389/fgene.2020.00614. eCollection 2020. Front Genet. 2020. PMID: 32655623 Free PMC article.

2

De Novo KCNQ2 Mutation in One Case of Epilepsy of Infancy With Migrating Focal Seizures That Evolved to Infantile Spasms.

Duan H, Peng J, Kessi M, Yin F. Duan H, et al. Among authors: kessi m. Child Neurol Open. 2018 Apr 11;5:2329048X18767738. doi: 10.1177/2329048X18767738. eCollection 2018. Child Neurol Open. 2018. PMID: 29687029 Free PMC article.

3

Next-generation sequencing improves treatment efficacy and reduces hospitalization in children with drug-resistant epilepsy.

Peng J, Pang N, Wang Y, Wang XL, Chen J, Xiong J, Peng P, Zhu CH, Kessi MB, He F, Yin F. Peng J, et al. CNS Neurosci Ther. 2019 Jan;25(1):14-20. doi: 10.1111/cns.12869. Epub 2018 Jun 22. CNS Neurosci Ther. 2019. PMID: 29933521 Free PMC article.

4

Genetic etiologies of the electrical status epilepticus during slow wave sleep: systematic review.

Kessi M, Peng J, Yang L, Xiong J, Duan H, Pang N, Yin F. Kessi M, et al. BMC Genet. 2018 Jul 6;19(1):40. doi: 10.1186/s12863-018-0628-5. BMC Genet. 2018. PMID: 29976148 Free PMC article.

5

A Case With 4 de Novo Copy Number Variations With Clinical Features That Overlap 1q43q44 Microdeletion and 3q29 Microduplication Syndromes.

Kessi M, Peng J, Yang L, Duan H, Tang Y, Yin F. Kessi M, et al. Child Neurol Open. 2018 Sep 24;5:2329048X18798200. doi: 10.1177/2329048X18798200. eCollection 2018. Child Neurol Open. 2018. PMID: 30263904 Free PMC article.

6

[A family with Allan-Herndon-Dudley syndrome due to SLC16A2 gene mutation].

Tang YL, Peng J, Xiong J, Pang N, Wu LW, Yang HY, Kessi M, Yin F. Tang YL, et al. Among authors: kessi m. Zhonghua Er Ke Za Zhi. 2018 Nov 2;56(11):829-834. doi: 10.3760/cma.j.issn.0578-1310.2018.11.008. Zhonghua Er Ke Za Zhi. 2018. PMID: 30392207 Chinese.

7

Rare Copy Number Variations and Predictors in Children With Intellectual Disability and Epilepsy.

Kessi M, Xiong J, Wu L, Yang L, He F, Chen C, Pang N, Duan H, Zhang W, Arafat A, Yin F, Peng J. Kessi M, et al. Front Neurol. 2018 Nov 19;9:947. doi: 10.3389/fneur.2018.00947. eCollection 2018. Front Neurol. 2018. PMID: 30510536 Free PMC article.

8

Myelin Oligodendrocyte Glycoprotein (MOG) Antibody Diseases in Children in Central South China: Clinical Features, Treatments, Influencing Factors, and Outcomes.

Mao L, Yang L, Kessi M, He F, Zhang C, Wu L, Yin F, Peng J. Mao L, et al. Among authors: kessi m. Front Neurol. 2019 Aug 8;10:868. doi: 10.3389/fneur.2019.00868. eCollection 2019. Front Neurol. 2019. PMID: 31440204 Free PMC article.

9

Efficacy of different treatment modalities for acute and chronic phases of the febrile infection-related epilepsy syndrome: A systematic review.

Kessi M, Liu F, Zhan Y, Tang Y, Wu L, Yang L, Zhang CL, Yin F, Peng J. Kessi M, et al. Seizure. 2020 Jul;79:61-68. doi: 10.1016/j.seizure.2020.04.015. Epub 2020 May 14. Seizure. 2020. PMID: 32417686 Free article.

10

The Study of Genetic Susceptibility and Mitochondrial Dysfunction in Mesial Temporal Lobe Epilepsy.

Yang H, Yin F, Gan S, Pan Z, Xiao T, Kessi M, Yang Z, Zhang VW, Wu L. Yang H, et al. Among authors: kessi m. Mol Neurobiol. 2020 Sep;57(9):3920-3930. doi: 10.1007/s12035-020-01993-4. Epub 2020 Jul 6. Mol Neurobiol. 2020. PMID: 32632602

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