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Journal Abstract Search

236 related items for PubMed ID: 10908896

  • 1.
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  • 2. Paroxysmal kinesigenic dyskinesia and generalized seizures: clinical and genetic analysis in a Spanish pedigree.
    Cuenca-Leon E, Cormand B, Thomson T, Macaya A.
    Neuropediatrics; 2002 Dec; 33(6):288-93. PubMed ID: 12571782
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  • 3. Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: evidence for a third EKD gene.
    Spacey SD, Valente EM, Wali GM, Warner TT, Jarman PR, Schapira AH, Dixon PH, Davis MB, Bhatia KP, Wood NW.
    Mov Disord; 2002 Jul; 17(4):717-25. PubMed ID: 12210861
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  • 4. Paroxysmal kinesigenic choreoathetosis locus maps to chromosome 16p11.2-q12.1.
    Tomita Ha, Nagamitsu S, Wakui K, Fukushima Y, Yamada K, Sadamatsu M, Masui A, Konishi T, Matsuishi T, Aihara M, Shimizu K, Hashimoto K, Mineta M, Matsushima M, Tsujita T, Saito M, Tanaka H, Tsuji S, Takagi T, Nakamura Y, Nanko S, Kato N, Nakane Y, Niikawa N.
    Am J Hum Genet; 1999 Dec; 65(6):1688-97. PubMed ID: 10577923
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  • 5. Locus for paroxysmal kinesigenic dyskinesia maps to human chromosome 16.
    Guerrini R, Parmeggiani L, Bonanni P, Carrozzo R, Casari G.
    Neurology; 2000 Sep 12; 55(5):738-9. PubMed ID: 10980756
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  • 6. A locus for paroxysmal kinesigenic dyskinesia maps to human chromosome 16.
    Bennett LB, Roach ES, Bowcock AM.
    Neurology; 2000 Jan 11; 54(1):125-30. PubMed ID: 10636137
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  • 7. Infantile convulsions and paroxysmal choreoathetosis in a consanguineous family.
    Demir E, Prud'homme JF, Topçu M.
    Pediatr Neurol; 2004 May 11; 30(5):349-53. PubMed ID: 15165638
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  • 8. A second paroxysmal kinesigenic choreoathetosis locus (EKD2) mapping on 16q13-q22.1 indicates a family of genes which give rise to paroxysmal disorders on human chromosome 16.
    Valente EM, Spacey SD, Wali GM, Bhatia KP, Dixon PH, Wood NW, Davis MB.
    Brain; 2000 Oct 11; 123 ( Pt 10)():2040-5. PubMed ID: 11004121
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  • 9. Familial infantile convulsions and paroxysmal choreoathetosis: a new neurological syndrome linked to the pericentromeric region of human chromosome 16.
    Szepetowski P, Rochette J, Berquin P, Piussan C, Lathrop GM, Monaco AP.
    Am J Hum Genet; 1997 Oct 11; 61(4):889-98. PubMed ID: 9382100
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  • 11. Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: new diagnostic criteria.
    Bruno MK, Hallett M, Gwinn-Hardy K, Sorensen B, Considine E, Tucker S, Lynch DR, Mathews KD, Swoboda KJ, Harris J, Soong BW, Ashizawa T, Jankovic J, Renner D, Fu YH, Ptacek LJ.
    Neurology; 2004 Dec 28; 63(12):2280-7. PubMed ID: 15623687
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  • 12. Idiopathic epilepsy and paroxysmal dyskinesia.
    Guerrini R.
    Epilepsia; 2001 Dec 28; 42 Suppl 3():36-41. PubMed ID: 11520321
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  • 13. 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 28; 12(3):199-204. PubMed ID: 20716510
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  • 14. Co-segregation of benign infantile convulsions and paroxysmal kinesigenic choreoathetosis.
    Hattori H, Fujii T, Nigami H, Higuchi Y, Tsuji M, Hamada Y.
    Brain Dev; 2000 Oct 28; 22(7):432-5. PubMed ID: 11102728
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  • 19. Paroxysmal kinesigenic choreoathetosis: from first discovery in 1892 to genetic linkage with benign familial infantile convulsions.
    Kato N, Sadamatsu M, Kikuchi T, Niikawa N, Fukuyama Y.
    Epilepsy Res; 2006 Aug 28; 70 Suppl 1():S174-84. PubMed ID: 16901678
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