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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

231 related articles for article (PubMed ID: 24465263)

  • 1. Clinical manifestations in paroxysmal kinesigenic dyskinesia patients with proline-rich transmembrane protein 2 gene mutation.
    Youn J; Kim JS; Lee M; Lee J; Roh H; Ki CS; Choa JW
    J Clin Neurol; 2014 Jan; 10(1):50-4. PubMed ID: 24465263
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. Genetic and phenotypic analyses of PRRT2 positive and negative paroxysmal kinesigenic dyskinesia.
    Zhang Y; Ren J; Yang T; Xiong W; Qin L; An D; Hu F; Zhou D
    Ther Adv Neurol Disord; 2024; 17():17562864231224110. PubMed ID: 38250317
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. PRRT2 mutations: a major cause of paroxysmal kinesigenic dyskinesia in the European population.
    Méneret A; Grabli D; Depienne C; Gaudebout C; Picard F; Dürr A; Lagroua I; Bouteiller D; Mignot C; Doummar D; Anheim M; Tranchant C; Burbaud P; Jedynak CP; Gras D; Steschenko D; Devos D; Billette de Villemeur T; Vidailhet M; Brice A; Roze E
    Neurology; 2012 Jul; 79(2):170-4. PubMed ID: 22744660
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Novel mutation of the
    Fang J; Wang S; Zhao G; Cao L
    Biomed Rep; 2020 Jun; 12(6):309-312. PubMed ID: 32346475
    [TBL] [Abstract][Full Text] [Related]  

  • 9.
    Motoyama R; Matsudaira T; Terada K; Usui N; Yoshiura KI; Takahashi Y
    Epilepsy Behav Rep; 2022; 19():100554. PubMed ID: 35712060
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. TMEM151A Variants Cause Paroxysmal Kinesigenic Dyskinesia: A Large-Sample Study.
    Tian WT; Zhan FX; Liu ZH; Liu Z; Liu Q; Guo XN; Zhou ZW; Wang SG; Liu XR; Jiang H; Li XH; Zhao GH; Li HY; Tang JG; Bi GH; Zhong P; Yin XM; Liu TT; Ni RL; Zheng HR; Liu XL; Qian XH; Wu JY; Cao YW; Zhang C; Liu SH; Wu YY; Wang QF; Xu T; Hou WZ; Li ZY; Ke HY; Zhu ZY; Zheng L; Wang T; Rong TY; Wu L; Zhang Y; Fang K; Wang ZH; Zhang YK; Zhang M; Zhao YW; Tang BS; Luan XH; Huang XJ; Cao L
    Mov Disord; 2022 Mar; 37(3):545-552. PubMed ID: 34820915
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Five cases of paroxysmal kinesigenic dyskinesia by genetic diagnosis.
    Chen GH
    Exp Ther Med; 2015 Mar; 9(3):909-912. PubMed ID: 25667652
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. [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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 12.