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 *

246 related articles for article (PubMed ID: 12210861)

  • 1. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Paroxysmal kinesigenic dyskinesia and infantile convulsions: clinical and linkage studies.
    Swoboda KJ; Soong B; McKenna C; Brunt ER; Litt M; Bale JF; Ashizawa T; Bennett LB; Bowcock AM; Roach ES; Gerson D; Matsuura T; Heydemann PT; Nespeca MP; Jankovic J; Leppert M; Ptácek LJ
    Neurology; 2000 Jul; 55(2):224-30. PubMed ID: 10908896
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome.
    Winkelmann J; Lichtner P; Pütz B; Trenkwalder C; Hauk S; Meitinger T; Strom T; Muller-Myhsok B
    Mov Disord; 2006 Jan; 21(1):28-33. PubMed ID: 16124010
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Familial paroxysmal dystonic choreoathetosis and its differentiation from related syndromes.
    Lance JW
    Ann Neurol; 1977 Oct; 2(4):285-93. PubMed ID: 617268
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Recent advances of genetic research on paroxysmal kinesigenic dyskinesias].
    Li XH; Chen SQ; Wang YM
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Aug; 25(4):410-3. PubMed ID: 18683138
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A locus for paroxysmal kinesigenic dyskinesia maps to human chromosome 16.
    Bennett LB; Roach ES; Bowcock AM
    Neurology; 2000 Jan; 54(1):125-30. PubMed ID: 10636137
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic heterogeneity in paroxysmal nonkinesigenic dyskinesia.
    Spacey SD; Adams PJ; Lam PC; Materek LA; Stoessl AJ; Snutch TP; Hsiung GY
    Neurology; 2006 May; 66(10):1588-90. PubMed ID: 16717228
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 63(12):2280-7. PubMed ID: 15623687
    [TBL] [Abstract][Full Text] [Related]  

  • 11. PRRT2 phenotypes and penetrance of paroxysmal kinesigenic dyskinesia and infantile convulsions.
    van Vliet R; Breedveld G; de Rijk-van Andel J; Brilstra E; Verbeek N; Verschuuren-Bemelmans C; Boon M; Samijn J; Diderich K; van de Laar I; Oostra B; Bonifati V; Maat-Kievit A
    Neurology; 2012 Aug; 79(8):777-84. PubMed ID: 22875091
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Locus for paroxysmal kinesigenic dyskinesia maps to human chromosome 16.
    Guerrini R; Parmeggiani L; Bonanni P; Carrozzo R; Casari G
    Neurology; 2000 Sep; 55(5):738-9. PubMed ID: 10980756
    [No Abstract]   [Full Text] [Related]  

  • 14. Paroxysmal kinesigenic choreoathetosis.
    Boel M; Casaer P
    Neuropediatrics; 1984 Oct; 15(4):215-7. PubMed ID: 6493453
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 123 ( Pt 10)():2040-5. PubMed ID: 11004121
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 70 Suppl 1():S174-84. PubMed ID: 16901678
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Familial dyskinesia and facial myokymia (FDFM): a novel movement disorder.
    Fernandez M; Raskind W; Wolff J; Matsushita M; Yuen E; Graf W; Lipe H; Bird T
    Ann Neurol; 2001 Apr; 49(4):486-92. PubMed ID: 11310626
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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; 22(7):432-5. PubMed ID: 11102728
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Epilepsy and paroxysmal movement disorders in families: evidence for shared mechanisms.
    Singh R; Macdonell RA; Scheffer IE; Crossland KM; Berkovic SF
    Epileptic Disord; 1999 Jun; 1(2):93-9. PubMed ID: 10937138
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Clinical study and genetic 3q28 locus linkage in 2 Swiss families with Kjer dominant optic atrophy (OPA1)].
    Lefèvre A; Hiroz C; Zografos L; Schorderet DF; Munier FL
    Klin Monbl Augenheilkd; 1998 May; 212(5):301-4. PubMed ID: 9677562
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.