174 related articles for article (PubMed ID: 29379546)
1. GABRG2 C588T gene polymorphisms might be a predictive genetic marker of febrile seizures and generalized recurrent seizures: a case-control study in a Romanian pediatric population.
Butilă AT; Zazgyva A; Sin AI; Szabo ER; Tilinca MC
Arch Med Sci; 2018 Jan; 14(1):157-166. PubMed ID: 29379546
[TBL] [Abstract][Full Text] [Related]
2. Role of MDR1 C3435T and GABRG2 C588T gene polymorphisms in seizure occurrence and MDR1 effect on anti-epileptic drug (phenytoin) absorption.
Ponnala S; Chaudhari JR; Jaleel MA; Bhiladvala D; Kaipa PR; Das UN; Hasan Q
Genet Test Mol Biomarkers; 2012 Jun; 16(6):550-7. PubMed ID: 22239287
[TBL] [Abstract][Full Text] [Related]
3. GABRG2 gene polymorphisms in Egyptian children with simple febrile seizures.
Salam SM; Rahman HM; Karam RA
Indian J Pediatr; 2012 Nov; 79(11):1514-6. PubMed ID: 21983990
[TBL] [Abstract][Full Text] [Related]
4. A splice-site mutation in GABRG2 associated with childhood absence epilepsy and febrile convulsions.
Kananura C; Haug K; Sander T; Runge U; Gu W; Hallmann K; Rebstock J; Heils A; Steinlein OK
Arch Neurol; 2002 Jul; 59(7):1137-41. PubMed ID: 12117362
[TBL] [Abstract][Full Text] [Related]
5.
Saleem T; Maqbool H; Sheikh N; Tayyeb A; Mukhtar M; Ashfaq A
Biomed Res Int; 2022; 2022():3460792. PubMed ID: 36425336
[TBL] [Abstract][Full Text] [Related]
6. Contribution of GABRG2 Polymorphisms to Risk of Epilepsy and Febrile Seizure: a Multicenter Cohort Study and Meta-analysis.
Haerian BS; Baum L; Kwan P; Cherny SS; Shin JG; Kim SE; Han BG; Tan HJ; Raymond AA; Tan CT; Mohamed Z
Mol Neurobiol; 2016 Oct; 53(8):5457-67. PubMed ID: 26452361
[TBL] [Abstract][Full Text] [Related]
7. Association of rs211037 GABRG2 gene polymorphism with susceptibility to idiopathic generalized epilepsy.
Milanovska M; Cvetkovska E; Panov S
Med Glas (Zenica); 2021 Aug; 18(2):404-409. PubMed ID: 34080406
[TBL] [Abstract][Full Text] [Related]
8. GABRG2, rs211037 is associated with epilepsy susceptibility, but not with antiepileptic drug resistance and febrile seizures.
Balan S; Sathyan S; Radha SK; Joseph V; Radhakrishnan K; Banerjee M
Pharmacogenet Genomics; 2013 Nov; 23(11):605-10. PubMed ID: 24061200
[TBL] [Abstract][Full Text] [Related]
9. Analysis of GABRG2 C588T polymorphism in genetic epilepsy and evaluation of GABRG2 in drug treatment.
Wang S; Zhang X; Zhou L; Wu Q; Han Y
Clin Transl Sci; 2021 Sep; 14(5):1725-1733. PubMed ID: 33650258
[TBL] [Abstract][Full Text] [Related]
10. GABRG2 rs211037 polymorphism and epilepsy: a systematic review and meta-analysis.
Haerian BS; Baum L
Seizure; 2013 Jan; 22(1):53-8. PubMed ID: 23140995
[TBL] [Abstract][Full Text] [Related]
11. The likelihood approach for potential role of "GABRG2 (C588T, C315T) gene polymorphisms" on the poor response to carbamazepine therapy in Pakhtun population of Pakistan.
Ullah S; Ali N; Ahmad S; Sha SWA; Ali S; Almarshad F
Medicine (Baltimore); 2022 Oct; 101(40):e30948. PubMed ID: 36221407
[TBL] [Abstract][Full Text] [Related]
12. Association analysis of gamma 2 subunit of gamma- aminobutyric acid type A receptor polymorphisms with febrile seizures.
Chou IC; Peng CT; Huang CC; Tsai JJ; Tsai FJ; Tsai CH
Pediatr Res; 2003 Jul; 54(1):26-9. PubMed ID: 12672902
[TBL] [Abstract][Full Text] [Related]
13. The genetic variant "C588T" of GABARG2 is linked to childhood idiopathic generalized epilepsy and resistance to antiepileptic drugs.
Abou El Ella SS; Tawfik MA; Abo El Fotoh WMM; Soliman OAM
Seizure; 2018 Aug; 60():39-43. PubMed ID: 29894917
[TBL] [Abstract][Full Text] [Related]
14. Association between
Ma M; Zhao J; Xie D; Chen J
J Integr Neurosci; 2023 Oct; 22(6):151. PubMed ID: 38176934
[TBL] [Abstract][Full Text] [Related]
15. Generalized epilepsy with febrile seizures plus (GEFS+): clinical spectrum in seven Italian families unrelated to SCN1A, SCN1B, and GABRG2 gene mutations.
Bonanni P; Malcarne M; Moro F; Veggiotti P; Buti D; Ferrari AR; Parrini E; Mei D; Volzone A; Zara F; Heron SE; Bordo L; Marini C; Guerrini R
Epilepsia; 2004 Feb; 45(2):149-58. PubMed ID: 14738422
[TBL] [Abstract][Full Text] [Related]
16. Interleukin-1β and interleukin-1receptor antagonist polymorphisms in Egyptian children with febrile seizures: A case-control study.
Al Morshedy S; Elsaadany HF; Ibrahim HE; Sherif AM; Farghaly MAA; Allah MAN; Abouzeid H; Elashkar SSA; Hamed ME; Fathy MM; Khalil AM; Noah MA; Hegab MS; Ahmed AR; Hashem MIA; Emam AA; Anany HG; Ibrahim BR; Gawish HH; Nabil RM; Fattah LA; Alsayed SF
Medicine (Baltimore); 2017 Mar; 96(11):e6370. PubMed ID: 28296777
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Interleukin-6 gene polymorphisms in Egyptian children with febrile seizures: a case-control study.
Azab SF; Abdalhady MA; Ali A; Amin EK; Sarhan DT; Elhindawy EM; Almalky MA; Elhewala AA; Salam MM; Hashem MI; Soliman AA; Akeel NE; Abdellatif SH; Ismail SM; Elsamad NA; Arafat MS; Rass AA; Basset MA
Ital J Pediatr; 2016 Mar; 42():31. PubMed ID: 26960986
[TBL] [Abstract][Full Text] [Related]
19. SCN1A IVS5N+5 G>A Polymorphism and Risk of Febrile Seizure and Epilepsy: A Systematic Review and Meta-Analysis.
Hao J; Liu H; Ma J; Liu G; Dong G; Liu P; Xiao F
Front Neurol; 2020; 11():581539. PubMed ID: 33391151
[No Abstract] [Full Text] [Related]
20. SCN1A, SCN1B, and GABRG2 gene mutation analysis in Chinese families with generalized epilepsy with febrile seizures plus.
Sun H; Zhang Y; Liang J; Liu X; Ma X; Wu H; Xu K; Qin J; Qi Y; Wu X
J Hum Genet; 2008; 53(8):769-774. PubMed ID: 18566737
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
