Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Public Health Genomics and Precision Health Knowledge Base (v6.0)

Note: Javascript is disabled or is not supported by your browser. For this reason, some items on this page will be unavailable. For more information about this message, please visit this page: About CDC.gov.

HuGE Navigator|HuGE Literature Finder|PHGKB

HuGE Literature Finder

Records 1-8

Query Trace: Movement Disorders and PRRT2[orginal query]

Paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 110 patients. Neurology 2015 Oct . Huang Xiao-Jun, Wang Tian, Wang Jun-Ling, Liu Xiao-Li, Che Xiang-Qian, Li Jin, Mao Xiao, Zhang Mei, Bi Guang-Hui, Wu Li, Zhang Yu, Wang Jing-Yi, Shen Jun-Yi, Tang Bei-Sha, Cao Li, Chen Sheng- Similar articles in PubMed
Genotype-phenotype correlation in a cohort of paroxysmal kinesigenic dyskinesia cases. Journal of the neurological sciences 2014 May 340 (1-2): 91-3. Mao Cheng-Yuan, Shi Chang-He, Song Bo, Wu Jun, Ji Yan, Qin Jie, Li Yu-Sheng, Wang Jing-Jing, Shang Dan-Dan, Sun Shi-Lei, Xu Yu-Mi Similar articles in PubMed
Clinico-genetic comparisons of paroxysmal kinesigenic dyskinesia patients with and without PRRT2 mutations. European journal of neurology : the official journal of the European Federation of Neurological Societies 2014 Apr 21 (4): 674-8. Tan L C S, Methawasin K, Teng E W L, Ng A R J, Seah S H, Au W L, Liu J J, Foo J N, Zhao Y, Tan E Similar articles in PubMed
Novel PRRT2 mutations in paroxysmal dyskinesia patients with variant inheritance and phenotypes. Genes, brain, and behavior 2013 Mar 12 (2): 234-40. Liu X-R, Wu M, He N, Meng H, Wen L, Wang J-L, Zhang M-P, Li W-B, Mao X, Qin J-M, Li B-M, Tang B, Deng Y-H, Shi Y-W, Su T, Yi Y-H, Tang B-S, Liao W Similar articles in PubMed
PRRT2 mutation screening in patients with paroxysmal kinesigenic dyskinesia from Southwest China. European journal of neurology : the official journal of the European Federation of Neurological Societies 2013 Mar . Chen YP, Song W, Yang J, Zheng ZZ, Huang R, Chen K, Zhao B, Chen XP, Burgunder JM, Shang HF Similar articles in PubMed
Genetic analysis of PRRT2 for benign infantile epilepsy, infantile convulsions with choreoathetosis syndrome, and benign convulsions with mild gastroenteritis. Brain & development 2012 Oct . 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 Similar articles in PubMed
PRRT2 gene mutations: From paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine. Neurology 2012 Oct . Gardiner AR, Bhatia KP, Stamelou M, Dale RC, Kurian MA, Schneider SA, Wali GM, Counihan T, Schapira AH, Spacey SD, Valente EM, Silveira-Moriyama L, Teive HA, Raskin S, Sander JW, Lees A, Warner T, Kullmann DM, Wood NW, Hanna M, Houlden H Similar articles in PubMed
Mutation Analysis of MR-1, SLC2A1, and CLCN1 in 28 PRRT2-negative Paroxysmal Kinesigenic Dyskinesia Patients. Chinese medical journal 0 129 (9): 1017-1021. Wang Hong-Xia, Li Hong-Fu, Liu Gong-Lu, Wen Xiao-Dan, Wu Zhi-Yi Similar articles in PubMed

File Formats Help:

How do I view different file formats (PDF, DOC, PPT, MPEG) on this site?

Page last reviewed:Jul 30, 2019
Page last updated:Oct 10, 2019
Content source:

TOP