177 related articles for article (PubMed ID: 38249294)
1.
He YY; Luo S; Jin L; Wang PY; Xu J; Jiao HL; Yan HJ; Wang Y; Zhai QX; Ji JJ; Zhang WJ; Zhou P; Li H; Liao WP; Lan S; Xu L
Front Mol Neurosci; 2023; 16():1290919. PubMed ID: 38249294
[TBL] [Abstract][Full Text] [Related]
2.
Luo S; Ye XG; Jin L; Li H; He YY; Guan BZ; Gao LD; Liang XY; Wang PY; Lu XG; Yan HJ; Li BM; Chen YJ; Liu ZG
Front Mol Neurosci; 2023; 16():1162408. PubMed ID: 37213690
[TBL] [Abstract][Full Text] [Related]
3.
Bian WJ; Li ZJ; Wang J; Luo S; Li BM; Gao LD; He N; Yi YH
Front Mol Neurosci; 2022; 15():862480. PubMed ID: 35663265
[TBL] [Abstract][Full Text] [Related]
4. MED12 variants associated with X-linked recessive partial epilepsy without intellectual disability.
Yang JH; Liu ZG; Liu CL; Zhang MR; Jia YL; Zhai QX; He MF; He N; Qiao JD
Seizure; 2024 Mar; 116():30-36. PubMed ID: 36894399
[TBL] [Abstract][Full Text] [Related]
5. DYNC1H1 variants associated with infant-onset epilepsy without neurodevelopmental disorders.
Wu WC; Liang XY; Zhang DM; Jin L; Liu ZG; Zeng XL; Zhai QX; Liao WP; He N; Meng XH
Seizure; 2024 Mar; 116():119-125. PubMed ID: 37903666
[TBL] [Abstract][Full Text] [Related]
6. Recessive
Wang JY; Wang J; Lu XG; Song W; Luo S; Zou DF; Hua LD; Peng Q; Tian Y; Gao LD; Liao WP; He N
Front Mol Neurosci; 2022; 15():861159. PubMed ID: 35620448
[TBL] [Abstract][Full Text] [Related]
7. Reprint of: Recessive APC2 missense variants associated with epilepsies without neurodevelopmental disorders.
Jin L; Li Y; Luo S; Peng Q; Zhai QX; Zhai JX; Gao LD; Guo JJ; Song W; Yi YH; He N; Chen YJ
Seizure; 2024 Mar; 116():87-92. PubMed ID: 38523034
[TBL] [Abstract][Full Text] [Related]
8. Recessive APC2 missense variants associated with epilepsies without neurodevelopmental disorders.
Jin L; Li Y; Luo S; Peng Q; Zhai QX; Zhai JX; Gao LD; Guo JJ; Song W; Yi YH; He N; Chen YJ
Seizure; 2023 Oct; 111():172-177. PubMed ID: 37657306
[TBL] [Abstract][Full Text] [Related]
9. NEXMIF variants are associated with epilepsy with or without intellectual disability.
Ye ZL; Yan HJ; Guo QH; Zhang SQ; Luo S; Lian YJ; Ma YQ; Lu XG; Liu XR; Shen NX; Gao LD; Chen Z; Shi YW
Seizure; 2024 Mar; 116():93-99. PubMed ID: 37643945
[TBL] [Abstract][Full Text] [Related]
10. A Novel
Sandestig A; Green A; Aronsson J; Ellnebo K; Stefanova M
Mol Syndromol; 2020 Jan; 10(5):281-285. PubMed ID: 32021600
[TBL] [Abstract][Full Text] [Related]
11.
Liu WH; Luo S; Zhang DM; Lin ZS; Lan S; Li X; Shi YW; Su T; Yi YH; Zhou P; Li BM
Front Mol Neurosci; 2023; 16():1321090. PubMed ID: 38269327
[TBL] [Abstract][Full Text] [Related]
12. Association of FAT1 with focal epilepsy and correlation between seizure relapse and gene expression stage.
Zou DF; Li XY; Lu XG; Wang HL; Song W; Zhang MW; Liu XR; Li BM; Liao JX; Zhong JM; Meng H; Li B
Seizure; 2024 Mar; 116():37-44. PubMed ID: 36941137
[TBL] [Abstract][Full Text] [Related]
13. SCAF4 variants are associated with epilepsy with neurodevelopmental disorders.
Hu Y; Zhang B; Chen L; He J; Yang L; Chen X
Seizure; 2024 Mar; 116():113-118. PubMed ID: 37891035
[TBL] [Abstract][Full Text] [Related]
14. BCOR variants are associated with X-linked recessive partial epilepsy.
Li X; Bian WJ; Liu XR; Wang J; Luo S; Li BM; Yi YH; Wu QY; Zhai QX; Gao LD; Zhang HF; He N; Liao WP;
Epilepsy Res; 2022 Nov; 187():107036. PubMed ID: 36279688
[TBL] [Abstract][Full Text] [Related]
15. The molecular and phenotypic spectrum of CLCN4-related epilepsy.
He H; Guzman RE; Cao D; Sierra-Marquez J; Yin F; Fahlke C; Peng J; Stauber T
Epilepsia; 2021 Jun; 62(6):1401-1415. PubMed ID: 33951195
[TBL] [Abstract][Full Text] [Related]
16. Investigation of FRMPD4 variants associated with X-linked epilepsy.
Li RK; Li H; Tian MQ; Li Y; Luo S; Liang XY; Liu WH; Li BM; Shi XQ; Li J; Li B; Shu XM;
Seizure; 2024 Mar; 116():45-50. PubMed ID: 37330374
[TBL] [Abstract][Full Text] [Related]
17. Electroclinical Phenotype-Genotype Homogeneity in Drug-Resistant "Generalized" Tonic-Clonic Seizures of Early Childhood.
Jukkarwala A; Menon RN; Sunesh ER; Radhakrishnan A
Clin EEG Neurosci; 2021 Sep; 52(5):371-375. PubMed ID: 32880473
[TBL] [Abstract][Full Text] [Related]
18. Gain-of-function and loss-of-function variants in GRIA3 lead to distinct neurodevelopmental phenotypes.
Rinaldi B; Bayat A; Zachariassen LG; Sun JH; Ge YH; Zhao D; Bonde K; Madsen LH; Awad IAA; Bagiran D; Sbeih A; Shah SM; El-Sayed S; Lyngby SM; Pedersen MG; Stenum-Berg C; Walker LC; Krey I; Delahaye-Duriez A; Emrick LT; Sully K; Murali CN; Burrage LC; Plaud Gonzalez JA; Parnes M; Friedman J; Isidor B; Lefranc J; Redon S; Heron D; Mignot C; Keren B; Fradin M; Dubourg C; Mercier S; Besnard T; Cogne B; Deb W; Rivier C; Milani D; Bedeschi MF; Di Napoli C; Grilli F; Marchisio P; Koudijs S; Veenma D; Argilli E; Lynch SA; Au PYB; Ayala Valenzuela FE; Brown C; Masser-Frye D; Jones M; Patron Romero L; Li WL; Thorpe E; Hecher L; Johannsen J; Denecke J; McNiven V; Szuto A; Wakeling E; Cruz V; Sency V; Wang H; Piard J; Kortüm F; Herget T; Bierhals T; Condell A; Ben-Zeev B; Kaur S; Christodoulou J; Piton A; Zweier C; Kraus C; Micalizzi A; Trivisano M; Specchio N; Lesca G; Møller RS; Tümer Z; Musgaard M; Gerard B; Lemke JR; Shi YS; Kristensen AS
Brain; 2024 May; 147(5):1837-1855. PubMed ID: 38038360
[TBL] [Abstract][Full Text] [Related]
19. Gain-of-function variants in GABRD reveal a novel pathway for neurodevelopmental disorders and epilepsy.
Ahring PK; Liao VWY; Gardella E; Johannesen KM; Krey I; Selmer KK; Stadheim BF; Davis H; Peinhardt C; Koko M; Coorg RK; Syrbe S; Bertsche A; Santiago-Sim T; Diemer T; Fenger CD; Platzer K; Eichler EE; Lerche H; Lemke JR; Chebib M; Møller RS
Brain; 2022 May; 145(4):1299-1309. PubMed ID: 34633442
[TBL] [Abstract][Full Text] [Related]
20. PIGN encephalopathy: Characterizing the epileptology.
Bayat A; de Valles-Ibáñez G; Pendziwiat M; Knaus A; Alt K; Biamino E; Bley A; Calvert S; Carney P; Caro-Llopis A; Ceulemans B; Cousin J; Davis S; des Portes V; Edery P; England E; Ferreira C; Freeman J; Gener B; Gorce M; Heron D; Hildebrand MS; Jezela-Stanek A; Jouk PS; Keren B; Kloth K; Kluger G; Kuhn M; Lemke JR; Li H; Martinez F; Maxton C; Mefford HC; Merla G; Mierzewska H; Muir A; Monfort S; Nicolai J; Norman J; O'Grady G; Oleksy B; Orellana C; Orec LE; Peinhardt C; Pronicka E; Rosello M; Santos-Simarro F; Schwaibold EMC; Stegmann APA; Stumpel CT; Szczepanik E; Terczyńska I; Thevenon J; Tzschach A; Van Bogaert P; Vittorini R; Walsh S; Weckhuysen S; Weissman B; Wolfe L; Reymond A; De Nittis P; Poduri A; Olson H; Striano P; Lesca G; Scheffer IE; Møller RS; Sadleir LG
Epilepsia; 2022 Apr; 63(4):974-991. PubMed ID: 35179230
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]