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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]
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]
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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]