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.
210 related articles for article (PubMed ID: 22870186)
21. Mutations in PRRT2 responsible for paroxysmal kinesigenic dyskinesias also cause benign familial infantile convulsions. Ono S; Yoshiura K; Kinoshita A; Kikuchi T; Nakane Y; Kato N; Sadamatsu M; Konishi T; Nagamitsu S; Matsuura M; Yasuda A; Komine M; Kanai K; Inoue T; Osamura T; Saito K; Hirose S; Koide H; Tomita H; Ozawa H; Niikawa N; Kurotaki N J Hum Genet; 2012 May; 57(5):338-41. PubMed ID: 22399141 [TBL] [Abstract][Full Text] [Related]
22. Clinico-genetic comparisons of paroxysmal kinesigenic dyskinesia patients with and without PRRT2 mutations. Tan LC; Methawasin K; Teng EW; Ng AR; Seah SH; Au WL; Liu JJ; Foo JN; Zhao Y; Tan EK Eur J Neurol; 2014 Apr; 21(4):674-8. PubMed ID: 23551744 [TBL] [Abstract][Full Text] [Related]
23. 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]
24. [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]
25. 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]
26. A Novel Truncation Mutation of the Kita M; Kuwata Y; Murase N; Akiyama Y; Usui T Mov Disord Clin Pract; 2017; 4(4):625-628. PubMed ID: 30713971 [TBL] [Abstract][Full Text] [Related]
27. PRRT2 truncated mutations lead to nonsense-mediated mRNA decay in Paroxysmal Kinesigenic Dyskinesia. Wu L; Tang HD; Huang XJ; Zheng L; Liu XL; Wang T; Wang JY; Cao L; Chen SD Parkinsonism Relat Disord; 2014 Dec; 20(12):1399-404. PubMed ID: 25457817 [TBL] [Abstract][Full Text] [Related]
28. Genetic analysis of PRRT2 for benign infantile epilepsy, infantile convulsions with choreoathetosis syndrome, and benign convulsions with mild gastroenteritis. Ishii A; Yasumoto S; Ihara Y; Inoue T; Fujita T; Nakamura N; Ohfu M; Yamashita Y; Takatsuka H; Taga T; Miyata R; Ito M; Tsuchiya H; Matsuoka T; Kitao T; Murakami K; Lee WT; Kaneko S; Hirose S Brain Dev; 2013 Jun; 35(6):524-30. PubMed ID: 23073245 [TBL] [Abstract][Full Text] [Related]
29. Unusual variability of PRRT2 linked phenotypes within a family. Brueckner F; Kohl B; Puest B; Gassner S; Osseforth J; Lindenau M; Stodieck S; Biskup S; Lohmann E Eur J Paediatr Neurol; 2014 Jul; 18(4):540-2. PubMed ID: 24755245 [TBL] [Abstract][Full Text] [Related]
30. Clinical features of childhood-onset paroxysmal kinesigenic dyskinesia with PRRT2 gene mutations. Silveira-Moriyama L; Gardiner AR; Meyer E; King MD; Smith M; Rakshi K; Parker A; Mallick AA; Brown R; Vassallo G; Jardine PE; Guerreiro MM; Lees AJ; Houlden H; Kurian MA Dev Med Child Neurol; 2013 Apr; 55(4):327-34. PubMed ID: 23363396 [TBL] [Abstract][Full Text] [Related]
31. 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]
32. The evolving spectrum of PRRT2-associated paroxysmal diseases. Ebrahimi-Fakhari D; Saffari A; Westenberger A; Klein C Brain; 2015 Dec; 138(Pt 12):3476-95. PubMed ID: 26598493 [TBL] [Abstract][Full Text] [Related]
33. PRRT2 mutations are related to febrile seizures in epileptic patients. He ZW; Qu J; Zhang Y; Mao CX; Wang ZB; Mao XY; Deng ZY; Zhou BT; Yin JY; Long HY; Xiao B; Zhang Y; Zhou HH; Liu ZQ Int J Mol Sci; 2014 Dec; 15(12):23408-17. PubMed ID: 25522171 [TBL] [Abstract][Full Text] [Related]
34. 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]
35. PRRT2 c.649dupC mutation derived from de novo in paroxysmal kinesigenic dyskinesia. Li HF; Ni W; Xiong ZQ; Xu J; Wu ZY CNS Neurosci Ther; 2013 Jan; 19(1):61-5. PubMed ID: 23176561 [TBL] [Abstract][Full Text] [Related]
36. Benign infantile convulsions (IC) and subsequent paroxysmal kinesigenic dyskinesia (PKD) in a patient with 16p11.2 microdeletion syndrome. Weber A; Köhler A; Hahn A; Neubauer B; Müller U Neurogenetics; 2013 Nov; 14(3-4):251-3. PubMed ID: 24100940 [TBL] [Abstract][Full Text] [Related]
37. PRRT2 mutation in Japanese children with benign infantile epilepsy. Okumura A; Shimojima K; Kubota T; Abe S; Yamashita S; Imai K; Okanishi T; Enoki H; Fukasawa T; Tanabe T; Dibbens LM; Shimizu T; Yamamoto T Brain Dev; 2013 Aug; 35(7):641-6. PubMed ID: 23131349 [TBL] [Abstract][Full Text] [Related]
38. 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]
39. 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]
40. TMEM151A phenotypic spectrum includes paroxysmal kinesigenic dyskinesia with infantile convulsions. Wang H; Huang P; Zhu M; Fang X; Wu C; Hong D Neurol Sci; 2022 Oct; 43(10):6095-6099. PubMed ID: 35727387 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]