164 related articles for article (PubMed ID: 32246320)
1. Different experiences of two PRRT2-associated self-limited familial infantile epilepsy.
Zhao Q; Liu Z; Hu Y; Fang S; Zheng F; Li X; Li F; Lin Z
Acta Neurol Belg; 2020 Aug; 120(4):1025-1028. PubMed ID: 32246320
[TBL] [Abstract][Full Text] [Related]
2. PRRT2 variants and effectiveness of various antiepileptic drugs in self-limited familial infantile epilepsy.
Zhao Q; Hu Y; Liu Z; Fang S; Zheng F; Wang X; Li F; Li X; Lin Z
Seizure; 2021 Oct; 91():360-368. PubMed ID: 34298454
[TBL] [Abstract][Full Text] [Related]
3. Peri-ictal EEG in infants with PRRT2-related self-limited infantile epilepsy.
Fearn N; Macdonald-Laurs E; Moylan L; Howell KB
Epileptic Disord; 2023 Aug; 25(4):510-518. PubMed ID: 37170076
[TBL] [Abstract][Full Text] [Related]
4. PRRT2 mutations in Japanese patients with benign infantile epilepsy and paroxysmal kinesigenic dyskinesia.
Okumura A; Shimojima K; Kurahashi H; Numoto S; Shimada S; Ishii A; Ohmori I; Takahashi S; Awaya T; Kubota T; Sakakibara T; Ishihara N; Hattori A; Torisu H; Tohyama J; Inoue T; Haibara A; Nishida T; Yuhara Y; Miya K; Tanaka R; Hirose S; Yamamoto T
Seizure; 2019 Oct; 71():1-5. PubMed ID: 31154286
[TBL] [Abstract][Full Text] [Related]
5. Clinical features of patients with paroxysmal kinesigenic dyskinesia, mutation screening of PRRT2 and the effects of morning draughts of oxcarbazepine.
Pan G; Zhang L; Zhou S
BMC Pediatr; 2019 Nov; 19(1):439. PubMed ID: 31722684
[TBL] [Abstract][Full Text] [Related]
6. PRRT2 mutations in a cohort of Chinese families with paroxysmal kinesigenic dyskinesia and genotype-phenotype correlation reanalysis in literatures.
Zhao G; Liu X; Zhang Q; Wang K
Int J Neurosci; 2018 Aug; 128(8):751-760. PubMed ID: 29285950
[TBL] [Abstract][Full Text] [Related]
7. Phenotypes and PRRT2 mutations in Chinese families with benign familial infantile epilepsy and infantile convulsions with paroxysmal choreoathetosis.
Yang X; Zhang Y; Xu X; Wang S; Yang Z; Wu Y; Liu X; Wu X
BMC Neurol; 2013 Dec; 13():209. PubMed ID: 24370076
[TBL] [Abstract][Full Text] [Related]
8. The PRRT2 mutation c.649dupC is the so far most frequent cause of benign familial infantile convulsions.
Steinlein OK; Villain M; Korenke C
Seizure; 2012 Nov; 21(9):740-2. PubMed ID: 22877996
[TBL] [Abstract][Full Text] [Related]
9. PRRT2 phenotypes and penetrance of paroxysmal kinesigenic dyskinesia and infantile convulsions.
van Vliet R; Breedveld G; de Rijk-van Andel J; Brilstra E; Verbeek N; Verschuuren-Bemelmans C; Boon M; Samijn J; Diderich K; van de Laar I; Oostra B; Bonifati V; Maat-Kievit A
Neurology; 2012 Aug; 79(8):777-84. PubMed ID: 22875091
[TBL] [Abstract][Full Text] [Related]
10. PRRT2 is mutated in familial and non-familial benign infantile seizures.
Specchio N; Terracciano A; Trivisano M; Cappelletti S; Claps D; Travaglini L; Cusmai R; Marras CE; Zara F; Fusco L; Bertini E; Vigevano F
Eur J Paediatr Neurol; 2013 Jan; 17(1):77-81. PubMed ID: 22902423
[TBL] [Abstract][Full Text] [Related]
11. [Clinical characteristics and genetic features of benign infantile epilepsy with PRRT2 mutation].
Chen CH; Wu HS; Wang XH; Wang HM; Zhang S; Lyu JL; Ren XT; Fang F; Chen GH
Zhonghua Er Ke Za Zhi; 2018 Nov; 56(11):818-823. PubMed ID: 30392205
[No Abstract] [Full Text] [Related]
12. A novel
Lu JG; Bishop J; Cheyette S; Zhulin IB; Guo S; Sobreira N; Brenner SE
Cold Spring Harb Mol Case Stud; 2018 Feb; 4(1):. PubMed ID: 29167286
[TBL] [Abstract][Full Text] [Related]
13. Features Differ Between Paroxysmal Kinesigenic Dyskinesia Patients with PRRT2 and TMEM151A Variants.
Chen YL; Chen DF; Li HF; Wu ZY
Mov Disord; 2022 Mar; 37(3):608-613. PubMed ID: 35083789
[TBL] [Abstract][Full Text] [Related]
14. PRRT2-positive self-limited infantile epilepsy: Initial seizure characteristics and response to sodium channel blockers.
Lee J; Kim YO; Lim BC; Lee J
Epilepsia Open; 2023 Jun; 8(2):436-443. PubMed ID: 36775847
[TBL] [Abstract][Full Text] [Related]
15. [Clinical features and PRRT2 mutations in infantile convulsions with paroxysmal choreoathetosis].
Yang X; Zhang Y; Xu X; Wang S; Yang Z; Wu Y; Zhang X; Liu X; Wu X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Dec; 31(6):679-85. PubMed ID: 25449067
[TBL] [Abstract][Full Text] [Related]
16. A PRRT2 variant in a Chinese family with paroxysmal kinesigenic dyskinesia and benign familial infantile seizures results in loss of interaction with STX1B.
Ma H; Feng S; Deng X; Wang L; Zeng S; Wang C; Ma X; Sun H; Chen R; Du S; Mao J; Zhang X; Ma C; Jiang H; Zhang L; Tang B; Liu JY
Epilepsia; 2018 Aug; 59(8):1621-1630. PubMed ID: 30009426
[TBL] [Abstract][Full Text] [Related]
17. PRRT2 mutations in familial infantile seizures, paroxysmal dyskinesia, and hemiplegic migraine.
Marini C; Conti V; Mei D; Battaglia D; Lettori D; Losito E; Bruccini G; Tortorella G; Guerrini R
Neurology; 2012 Nov; 79(21):2109-14. PubMed ID: 23077026
[TBL] [Abstract][Full Text] [Related]
18. Familial PRRT2 mutation with heterogeneous paroxysmal disorders including paroxysmal torticollis and hemiplegic migraine.
Dale RC; Gardiner A; Antony J; Houlden H
Dev Med Child Neurol; 2012 Oct; 54(10):958-60. PubMed ID: 22845787
[TBL] [Abstract][Full Text] [Related]
19. Levetiracetam may be an unsuitable choice for patients with PRRT2-associated self-limited infantile epilepsy.
Tian Y; Shi Z; Cai J; Hou C; Wang X; Zhu H; Peng B; Shi K; Li X; Gong S; Chen WX
BMC Pediatr; 2023 Oct; 23(1):529. PubMed ID: 37880614
[TBL] [Abstract][Full Text] [Related]
20. Reduced Penetrance of PRRT2 Mutation in a Chinese Family With Infantile Convulsion and Choreoathetosis Syndrome.
Zhang LM; An Y; Pan G; Ding YF; Zhou YF; Yao YH; Wu BL; Zhou SZ
J Child Neurol; 2015 Sep; 30(10):1263-9. PubMed ID: 25403460
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]