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 *

124 related articles for article (PubMed ID: 25745790)

  • 1. Secondary paroxysmal kinesigenic dyskinesia associated with CLCN2 gene mutation.
    Hanagasi HA; Bilgiç B; Abbink TE; Hanagasi F; Tüfekçioğlu Z; Gürvit H; Başak N; van der Knaap MS; Emre M
    Parkinsonism Relat Disord; 2015 May; 21(5):544-6. PubMed ID: 25745790
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. Proline-rich transmembrane protein 2-negative paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 163 patients.
    Tian WT; Huang XJ; Mao X; Liu Q; Liu XL; Zeng S; Guo XN; Shen JY; Xu YQ; Tang HD; Yin XM; Zhang M; Tang WG; Liu XR; Tang BS; Chen SD; Cao L
    Mov Disord; 2018 Mar; 33(3):459-467. PubMed ID: 29356177
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Familial IBGC caused by SLC20A2 mutation presenting as paroxysmal kinesigenic dyskinesia.
    Zhu M; Zhu X; Wan H; Hong D
    Parkinsonism Relat Disord; 2014 Mar; 20(3):353-4. PubMed ID: 24411498
    [No Abstract]   [Full Text] [Related]  

  • 5. Mutations of proline-rich transmembrane protein-2 and paroxysmal kinesigenic dyskinesia in Taiwan.
    Chen YC; Lee YS; Shih CC; Wu T; Chen CM
    Mov Disord; 2013 Sep; 28(10):1459-60. PubMed ID: 23436308
    [No Abstract]   [Full Text] [Related]  

  • 6. Two faces of the same coin: benign familial infantile seizures and paroxysmal kinesigenic dyskinesia caused by PRRT2 mutations.
    Schmidt A; Kumar KR; Redyk K; Grünewald A; Leben M; Münchau A; Sue CM; Hagenah J; Hartmann H; Lohmann K; Christen HJ; Klein C
    Arch Neurol; 2012 May; 69(5):668-70. PubMed ID: 22782515
    [No Abstract]   [Full Text] [Related]  

  • 7. A common PRRT2 mutation in familial paroxysmal kinesigenic dyskinesia in Hong Kong: a case series of 16 patients.
    Law CY; Yeung WL; Cheung YF; Chan HF; Fung E; Hui J; Yung IO; Yuen YP; Chan AO; Lam CW
    Hong Kong Med J; 2016 Dec; 22(6):619-22. PubMed ID: 27920401
    [No Abstract]   [Full Text] [Related]  

  • 8. Clinical and polygraphic study of familial paroxysmal kinesigenic dyskinesia with PRRT2 mutation.
    Fabbri M; Marini C; Bisulli F; Di Vito L; Elia A; Guerrini R; Mei D; Tinuper P
    Epileptic Disord; 2013 Jun; 15(2):123-7. PubMed ID: 23771590
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Secondary Paroxysmal Kinesigenic Dyskinesia with a CASR Mutation.
    Qin L; Zhang Y; Sander JW; Zhou D; Xiong W
    Mov Disord; 2022 Mar; 37(3):643-644. PubMed ID: 34913197
    [No Abstract]   [Full Text] [Related]  

  • 10. A novel homozygous mutation of CLCN2 in a patient with characteristic brain MRI images - A first case of CLCN2-related leukoencephalopathy in Japan.
    Hoshi M; Koshimizu E; Miyatake S; Matsumoto N; Imamura A
    Brain Dev; 2019 Jan; 41(1):101-105. PubMed ID: 30077506
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Paroxysmal Kinesigenic Dyskinesia Secondary to Brain Calcification with a Homozygous MYORG Mutation.
    Zhang Y; Xiong W; Lu L; Sander JW; Zhou D
    Mov Disord; 2022 Jan; 37(1):233-235. PubMed ID: 34783389
    [No Abstract]   [Full Text] [Related]  

  • 12. Paroxysmal Kinesigenic Dyskinesia Secondary to Brain Calcification with a Homozygous MYORG Mutation.
    Du J; Zhu X; Liu J; Tan Y
    Mov Disord; 2021 Nov; 36(11):2699-2701. PubMed ID: 34346093
    [No Abstract]   [Full Text] [Related]  

  • 13. De Novo Mutation in TMEM151A and Paroxysmal Kinesigenic Dyskinesia.
    Wirth T; Méneret A; Drouot N; Rudolf G; Lagha Boukbiza O; Chelly J; Tranchant C; Piton A; Roze E; Anheim M
    Mov Disord; 2022 May; 37(5):1115-1117. PubMed ID: 35587630
    [No Abstract]   [Full Text] [Related]  

  • 14. Paroxysmal Kinesigenic Dyskinesia.
    Mallik R; Nandi SS
    J Assoc Physicians India; 2016 Apr; 64(4):77-78. PubMed ID: 27734647
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Paroxysmal kinesigenic dyskinesia in pseudohypoparathyroidism: is basal ganglia calcification a necessary finding?
    Kwon YJ; Jung JM; Choi JY; Kwon DY
    J Neurol Sci; 2015 Oct; 357(1-2):302-3. PubMed ID: 26187296
    [No Abstract]   [Full Text] [Related]  

  • 16. 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]  

  • 17. Mutations in ANO3 and GNAL gene in thirty-three isolated dystonia families.
    Ma LY; Wang L; Yang YM; Feng T; Wan XH
    Mov Disord; 2015 Apr; 30(5):743-4. PubMed ID: 25847575
    [No Abstract]   [Full Text] [Related]  

  • 18. A case of familial paroxysmal nonkinesigenic dyskinesia due to mutation of the PNKD gene in Chinese Mainland.
    Liang S; Yu X; Zhang S; Tai J
    Brain Res; 2015 Jan; 1595():120-6. PubMed ID: 25107857
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Two novel CLCN2 mutations accelerating chloride channel deactivation are associated with idiopathic generalized epilepsy.
    Saint-Martin C; Gauvain G; Teodorescu G; Gourfinkel-An I; Fedirko E; Weber YG; Maljevic S; Ernst JP; Garcia-Olivares J; Fahlke C; Nabbout R; LeGuern E; Lerche H; Poncer JC; Depienne C
    Hum Mutat; 2009 Mar; 30(3):397-405. PubMed ID: 19191339
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Brain imaging findings in CLCN2-related leukoencephalopathy.
    Abreu VS; Tarrio J; Pinto E; Figueiroa S; Alves JE
    Pediatr Radiol; 2023 May; 53(5):1027-1032. PubMed ID: 36565320
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.