Yang L - 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. Among authors: yang l. Front Genet. 2020 Jun 23;11:614. doi: 10.3389/fgene.2020.00614. eCollection 2020. Front Genet. 2020. PMID: 32655623 Free PMC article.

2

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. Among authors: yang l. BMC Genet. 2018 Jul 6;19(1):40. doi: 10.1186/s12863-018-0628-5. BMC Genet. 2018. PMID: 29976148 Free PMC article.

3

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. Among authors: yang l. Front Neurol. 2018 Nov 19;9:947. doi: 10.3389/fneur.2018.00947. eCollection 2018. Front Neurol. 2018. PMID: 30510536 Free PMC article.

4

Calcium channelopathies and intellectual disability: a systematic review.

Kessi M, Chen B, Peng J, Yan F, Yang L, Yin F. Kessi M, et al. Among authors: yang l. Orphanet J Rare Dis. 2021 May 13;16(1):219. doi: 10.1186/s13023-021-01850-0. Orphanet J Rare Dis. 2021. PMID: 33985586 Free PMC article. Review.

5

Urine Organic Acids as Metabolic Indicators for Global Developmental Delay/Intellectual Disability in Chinese Children.

Chen B, Zhan Y, Kessi M, Chen S, Xiong J, Deng X, Yang L, Peng J, Yin F, He F. Chen B, et al. Among authors: yang l. Front Mol Biosci. 2021 Dec 22;8:792319. doi: 10.3389/fmolb.2021.792319. eCollection 2021. Front Mol Biosci. 2021. PMID: 35036412 Free PMC article.

6

The Contribution of HCN Channelopathies in Different Epileptic Syndromes, Mechanisms, Modulators, and Potential Treatment Targets: A Systematic Review.

Kessi M, Peng J, Duan H, He H, Chen B, Xiong J, Wang Y, Yang L, Wang G, Kiprotich K, Bamgbade OA, He F, Yin F. Kessi M, et al. Among authors: yang l. Front Mol Neurosci. 2022 May 19;15:807202. doi: 10.3389/fnmol.2022.807202. eCollection 2022. Front Mol Neurosci. 2022. PMID: 35663267 Free PMC article.

7

Diagnosis of intellectual disability/global developmental delay via genetic analysis in a central region of China.

Liao LH, Chen C, Peng J, Wu LW, He F, Yang LF, Zhang CL, Wang GL, Peng P, Ma YP, Miao P, Yin F. Liao LH, et al. Chin Med J (Engl). 2019 Jul 5;132(13):1533-1540. doi: 10.1097/CM9.0000000000000295. Chin Med J (Engl). 2019. PMID: 31205075 Free PMC article.

8

Synaptopathology Involved in Autism Spectrum Disorder.

Guang S, Pang N, Deng X, Yang L, He F, Wu L, Chen C, Yin F, Peng J. Guang S, et al. Among authors: yang l. Front Cell Neurosci. 2018 Dec 21;12:470. doi: 10.3389/fncel.2018.00470. eCollection 2018. Front Cell Neurosci. 2018. PMID: 30627085 Free PMC article. Review.

9

Neurological Diseases With Autism Spectrum Disorder: Role of ASD Risk Genes.

Xiong J, Chen S, Pang N, Deng X, Yang L, He F, Wu L, Chen C, Yin F, Peng J. Xiong J, et al. Among authors: yang l. Front Neurosci. 2019 Apr 11;13:349. doi: 10.3389/fnins.2019.00349. eCollection 2019. Front Neurosci. 2019. PMID: 31031587 Free PMC article.

10

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: yang l. Front Neurol. 2019 Aug 8;10:868. doi: 10.3389/fneur.2019.00868. eCollection 2019. Front Neurol. 2019. PMID: 31440204 Free PMC article.

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