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Journal Abstract Search

329 related items for PubMed ID: 22464846

  • 1. Paroxysmal kinesigenic dyskinesia: cortical or non-cortical origin.
    van Strien TW, van Rootselaar AF, Hilgevoord AA, Linssen WH, Groffen AJ, Tijssen MA.
    Parkinsonism Relat Disord; 2012 Jun; 18(5):645-8. PubMed ID: 22464846
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  • 4. Novel PRRT2 mutations in paroxysmal dyskinesia patients with variant inheritance and phenotypes.
    Liu XR, Wu M, He N, Meng H, Wen L, Wang JL, Zhang MP, Li WB, Mao X, Qin JM, Li BM, Tang B, Deng YH, Shi YW, Su T, Yi YH, Tang BS, Liao WP.
    Genes Brain Behav; 2013 Mar; 12(2):234-40. PubMed ID: 23190448
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  • 7. Novel familial cases of ICCA (infantile convulsions with paroxysmal choreoathetosis) syndrome.
    Rochette J, Roll P, Fu YH, Lemoing AG, Royer B, Roubertie A, Berquin P, Motte J, Wong SW, Hunter A, Robaglia-Schlupp A, Ptacek LJ, Szepetowski P.
    Epileptic Disord; 2010 Sep; 12(3):199-204. PubMed ID: 20716510
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  • 9. 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
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  • 10. Re-evaluation of PRRT2 mutations in paroxysmal disorders.
    Guo XN, Lu Q, Zhou XQ, Liu Q, Zhang X, Cui LY.
    J Neurol; 2014 May; 261(5):951-3. PubMed ID: 24609974
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  • 15. Intronic PRRT2 mutation generates novel splice acceptor site and causes paroxysmal kinesigenic dyskinesia with infantile convulsions (PKD/IC) in a three generation family.
    Weber A, Kreth J, Müller U.
    BMC Med Genet; 2016 Mar 03; 17():16. PubMed ID: 26936445
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  • 20. 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 26; 13():209. PubMed ID: 24370076
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