277 related articles for article (PubMed ID: 26717662)
1. [Clinical features and PRRT2 gene mutation in paroxysmal kinesigenic dyskinesia].
Yang X; Zhang Y; Xu X; Yang Z; Wang S; Wu Y; Wu X
Zhonghua Er Ke Za Zhi; 2015 Aug; 53(8):621-5. PubMed ID: 26717662
[TBL] [Abstract][Full Text] [Related]
2. [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]
3. 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]
4. 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]
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. Paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 110 patients.
Huang XJ; Wang T; Wang JL; Liu XL; Che XQ; Li J; Mao X; Zhang M; Bi GH; Wu L; Zhang Y; Wang JY; Shen JY; Tang BS; Cao L; Chen SD
Neurology; 2015 Nov; 85(18):1546-53. PubMed ID: 26446061
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. Mutation analysis of PRRT2 in two Chinese BFIS families and nomenclature of PRRT2 related paroxysmal diseases.
Wang JL; Mao X; Hu ZM; Li JD; Li N; Guo JF; Jiang H; Shen L; Li J; Shi YT; Xia K; Liu JY; Liao WP; Tang BS
Neurosci Lett; 2013 Sep; 552():40-5. PubMed ID: 23896529
[TBL] [Abstract][Full Text] [Related]
11. Clinical and genetic features of paroxysmal kinesigenic dyskinesia in Italian patients.
Lamperti C; Invernizzi F; Solazzi R; Freri E; Carella F; Zeviani M; Zibordi F; Fusco C; Zorzi G; Granata T; Garavaglia B; Nardocci N
Eur J Paediatr Neurol; 2016 Jan; 20(1):152-7. PubMed ID: 26384010
[TBL] [Abstract][Full Text] [Related]
12. PRRT2 mutation screening in patients with paroxysmal kinesigenic dyskinesia from Southwest China.
Chen YP; Song W; Yang J; Zheng ZZ; Huang R; Chen K; Zhao B; Chen XP; Burgunder JM; Shang HF
Eur J Neurol; 2014; 21(1):174-6. PubMed ID: 23496026
[TBL] [Abstract][Full Text] [Related]
13. PRRT2-related disorders: further PKD and ICCA cases and review of the literature.
Becker F; Schubert J; Striano P; Anttonen AK; Liukkonen E; Gaily E; Gerloff C; Müller S; Heußinger N; Kellinghaus C; Robbiano A; Polvi A; Zittel S; von Oertzen TJ; Rostasy K; Schöls L; Warner T; Münchau A; Lehesjoki AE; Zara F; Lerche H; Weber YG
J Neurol; 2013 May; 260(5):1234-44. PubMed ID: 23299620
[TBL] [Abstract][Full Text] [Related]
14. A new genetic diagnosis strategy for paroxysmal kinesigenic dyskinesia: Targeted high-throughput detection of PRRT2 gene c.649 locus.
Wen M; Huang H; Huang F; Xu R; Zhang J; Fan JG; Zeng J; Jiang KW; Liu D; Huang HL; He QN
Mol Genet Genomic Med; 2024 May; 12(5):e2469. PubMed ID: 38778723
[TBL] [Abstract][Full Text] [Related]
15. Mutation Analysis of MR-1, SLC2A1, and CLCN1 in 28 PRRT2-negative Paroxysmal Kinesigenic Dyskinesia Patients.
Wang HX; Li HF; Liu GL; Wen XD; Wu ZY
Chin Med J (Engl); 2016 May; 129(9):1017-21. PubMed ID: 27098784
[TBL] [Abstract][Full Text] [Related]
16. Clinical characteristics and PRRT2 gene mutation analysis of sporadic patients with paroxysmal kinesigenic dyskinesia in China.
Zhang Y; Li L; Chen W; Gan J; Liu ZG
Clin Neurol Neurosurg; 2017 Aug; 159():25-28. PubMed ID: 28525812
[TBL] [Abstract][Full Text] [Related]
17. PRRT2 Mutation and Serum Cytokines in Paroxysmal Kinesigenic Dyskinesia.
Xu K; Huang SS; Yue DY; Li G; Zhu SQ; Liu XY
Curr Med Sci; 2022 Apr; 42(2):280-285. PubMed ID: 35438471
[TBL] [Abstract][Full Text] [Related]
18. Novel Locus for Paroxysmal Kinesigenic Dyskinesia Mapped to Chromosome 3q28-29.
Liu D; Zhang Y; Wang Y; Chen C; Li X; Zhou J; Song Z; Xiao B; Rasco K; Zhang F; Wen S; Li G
Sci Rep; 2016 May; 6():25790. PubMed ID: 27173777
[TBL] [Abstract][Full Text] [Related]
19. Clinical and genetic analyses of 150 patients with paroxysmal kinesigenic dyskinesia.
Liu X; Ke H; Qian X; Wang S; Zhan F; Li Z; Tian W; Huang X; Zhang B; Cao L
J Neurol; 2022 Sep; 269(9):4717-4728. PubMed ID: 35428900
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
