These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
258 related articles for article (PubMed ID: 35359574)
1. Phenotypic Spectrum and Prognosis of Epilepsy Patients With Yang Y; Niu X; Cheng M; Zeng Q; Deng J; Tian X; Wang Y; Yu J; Shi W; Wu W; Ma J; Li Y; Yang X; Zhang X; Jia T; Yang Z; Liao J; Sun Y; Zheng H; Sun S; Sun D; Jiang Y; Zhang Y Front Mol Neurosci; 2022; 15():809163. PubMed ID: 35359574 [TBL] [Abstract][Full Text] [Related]
2. GABRB3-related epilepsy: novel variants, clinical features and therapeutic implications. Yang Y; Zeng Q; Cheng M; Niu X; Xiangwei W; Gong P; Li W; Ma J; Zhang X; Yang X; Yang Z; Sun D; Zhou S; Liao J; Jiang Y; Zhang Y J Neurol; 2022 May; 269(5):2649-2665. PubMed ID: 34698933 [TBL] [Abstract][Full Text] [Related]
3. Phenotypic spectrum of patients with GABRB2 variants: from mild febrile seizures to severe epileptic encephalopathy. Yang Y; Xiangwei W; Zhang X; Xiao J; Chen J; Yang X; Jia T; Yang Z; Jiang Y; Zhang Y Dev Med Child Neurol; 2020 Oct; 62(10):1213-1220. PubMed ID: 32686847 [TBL] [Abstract][Full Text] [Related]
4. [Clinical phenotypes of epilepsy associated with GABRA1 gene variants]. Yang Y; Zhang YH; Chen JY; Ma JH; Sun D; Yang XL; Zhang J; Chen Y; Wu XR Zhonghua Er Ke Za Zhi; 2020 Feb; 58(2):118-122. PubMed ID: 32102148 [No Abstract] [Full Text] [Related]
6. Zeng Q; Yang Y; Duan J; Niu X; Chen Y; Wang D; Zhang J; Chen J; Yang X; Li J; Yang Z; Jiang Y; Liao J; Zhang Y Front Mol Neurosci; 2022; 15():809951. PubMed ID: 35431799 [TBL] [Abstract][Full Text] [Related]
7. [Clinical features of epilepsies associated with GABRB2 variants]. Yang Y; Zhang YH; Chen JY; Zhang J; Yang XL; Chen Y; Yang ZX; Wu XR Zhonghua Er Ke Za Zhi; 2019 Jul; 57(7):532-537. PubMed ID: 31269553 [No Abstract] [Full Text] [Related]
8. [Early infantile epileptic encephalopathy caused by PACS2 gene variation: three cases report and literature review]. Wu MJ; Hu CH; Ma JH; Hu JS; Liu ZS; Sun D Zhonghua Er Ke Za Zhi; 2021 Jul; 59(7):594-599. PubMed ID: 34405643 [No Abstract] [Full Text] [Related]
9. [Clinical characteristics and gene analysis of SYNGAP1-related epilepsy in children]. Tian XJ; Fang F; Ding CH; Ren XT; Wang X; Wang XF; Lyu JL; Jin H; Han TL; Deng J Zhonghua Er Ke Za Zhi; 2021 Dec; 59(12):1059-1064. PubMed ID: 34856666 [No Abstract] [Full Text] [Related]
10. [Clinical phenotypes and genetic features of epilepsy children with MBD5 gene variants]. Jing XW; Cheng MM; Niu XY; Yang Y; Yang XL; Yang ZX; Zhang YH Zhonghua Er Ke Za Zhi; 2022 Apr; 60(4):345-349. PubMed ID: 35385942 [No Abstract] [Full Text] [Related]
11. Hernandez CC; Shen Y; Hu N; Shen W; Narayanan V; Ramsey K; He W; Zou L; Macdonald RL Biomolecules; 2023 Feb; 13(3):. PubMed ID: 36979350 [TBL] [Abstract][Full Text] [Related]
12. [Genotypes and phenotypes of IQSEC2 gene variants related epilepsy]. Wang DH; Niu XY; Cheng MM; Chen Y; Yang Y; Yang XL; Yang ZX; Zhang YH Zhonghua Er Ke Za Zhi; 2022 Dec; 60(12):1317-1321. PubMed ID: 36444437 [No Abstract] [Full Text] [Related]
13. [Genetics and clinical phenotypes of epilepsy associated with chromosome 2q24.3 microdeletion]. Zhao N; Cheng MM; Yang Y; Niu XY; Chen Y; Yang XL; Zhang YH Zhonghua Er Ke Za Zhi; 2022 Nov; 60(11):1140-1146. PubMed ID: 36319147 [No Abstract] [Full Text] [Related]
14. The molecular and phenotypic spectrum of IQSEC2-related epilepsy. Zerem A; Haginoya K; Lev D; Blumkin L; Kivity S; Linder I; Shoubridge C; Palmer EE; Field M; Boyle J; Chitayat D; Gaillard WD; Kossoff EH; Willems M; Geneviève D; Tran-Mau-Them F; Epstein O; Heyman E; Dugan S; Masurel-Paulet A; Piton A; Kleefstra T; Pfundt R; Sato R; Tzschach A; Matsumoto N; Saitsu H; Leshinsky-Silver E; Lerman-Sagie T Epilepsia; 2016 Nov; 57(11):1858-1869. PubMed ID: 27665735 [TBL] [Abstract][Full Text] [Related]
15. Phenotypic and Genotypic Characteristics of Chen C; Fang F; Wang X; Lv J; Wang X; Jin H Front Mol Neurosci; 2022; 15():821012. PubMed ID: 35571373 [TBL] [Abstract][Full Text] [Related]
16. HCN1 pathogenic variants associated with childhood epilepsy in a cohort of Chinese patients. Yang Z; Kuang Z; Liao H; Gan S; Peng X; Yang H; Wu L Epileptic Disord; 2024 Feb; 26(1):90-97. PubMed ID: 38009841 [TBL] [Abstract][Full Text] [Related]
17. GABRG2 mutations in genetic epilepsy with febrile seizures plus: structure, roles, and molecular genetics. Li X; Guo S; Sun Y; Ding J; Chen C; Wu Y; Li P; Sun T; Wang X J Transl Med; 2024 Aug; 22(1):767. PubMed ID: 39143639 [TBL] [Abstract][Full Text] [Related]
18. [Genotypes and clinical features of neonatal-onset genetic epilepsy in 141 patients]. Chen JY; Yang Y; Niu XY; Zhang J; Chen Y; Yang XL; Yang ZX; Jiang YW; Zhang YH Zhonghua Er Ke Za Zhi; 2021 Sep; 59(9):767-771. PubMed ID: 34645217 [No Abstract] [Full Text] [Related]
19. [Genotype and phenotype of children with DEPDC5 gene variants related epilepsy]. Liu WW; Yang Y; Niu XY; Cheng MM; Wang S; Wu Y; Yang ZX; Liu XY; Cai LX; Jiang YW; Zhang YH Zhonghua Er Ke Za Zhi; 2021 Oct; 59(10):859-864. PubMed ID: 34587683 [No Abstract] [Full Text] [Related]
20. Expanding the phenotypic spectrum of GABRG2 variants: a recurrent GABRG2 missense variant associated with a severe phenotype. Zou F; McWalter K; Schmidt L; Decker A; Picker JD; Lincoln S; Sweetser DA; Briere LC; Harini C; ; Marsh E; Medne L; Wang RY; Leydiker K; Mower A; Visser G; Cuppen I; van Gassen KL; van der Smagt J; Yousaf A; Tennison M; Shanmugham A; Butler E; Richard G; McKnight D J Neurogenet; 2017; 31(1-2):30-36. PubMed ID: 28460589 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]