289 related articles for article (PubMed ID: 11346027)
21. Autosomal recessive rolandic epilepsy with paroxysmal exercise-induced dystonia and writer's cramp: delineation of the syndrome and gene mapping to chromosome 16p12-11.2.
Guerrini R; Bonanni P; Nardocci N; Parmeggiani L; Piccirilli M; De Fusco M; Aridon P; Ballabio A; Carrozzo R; Casari G
Ann Neurol; 1999 Mar; 45(3):344-52. PubMed ID: 10072049
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. [Non-epileptic paroxysmal movement disorders].
Klein C; Vieregge P
Nervenarzt; 1998 Aug; 69(8):647-59. PubMed ID: 9757415
[TBL] [Abstract][Full Text] [Related]
24. Paroxysmal movement disorders and episodic ataxias.
Fernández-Alvarez E; Perez-Dueñas B
Handb Clin Neurol; 2013; 112():847-52. PubMed ID: 23622292
[TBL] [Abstract][Full Text] [Related]
25. [Paroxysmal kinesigenic dyskinesia: 2 case reports].
Xu Y; Liu XZ; Gao XG
Beijing Da Xue Xue Bao Yi Xue Ban; 2014 Aug; 46(4):659-61. PubMed ID: 25131491
[TBL] [Abstract][Full Text] [Related]
26. Diagnosis and treatment of paroxysmal dyskinesias revisited.
Unterberger I; Trinka E
Ther Adv Neurol Disord; 2008 Sep; 1(2):4-11. PubMed ID: 21180566
[TBL] [Abstract][Full Text] [Related]
27. Mutations in PRRT2 result in paroxysmal dyskinesias with marked variability in clinical expression.
Liu Q; Qi Z; Wan XH; Li JY; Shi L; Lu Q; Zhou XQ; Qiao L; Wu LW; Liu XQ; Yang W; Liu Y; Cui LY; Zhang X
J Med Genet; 2012 Feb; 49(2):79-82. PubMed ID: 22209761
[TBL] [Abstract][Full Text] [Related]
28. Electroclinical picture of autosomal dominant nocturnal frontal lobe epilepsy in a Japanese family.
Ito M; Kobayashi K; Fujii T; Okuno T; Hirose S; Iwata H; Mitsudome A; Kaneko S
Epilepsia; 2000 Jan; 41(1):52-8. PubMed ID: 10643924
[TBL] [Abstract][Full Text] [Related]
29. 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
[TBL] [Abstract][Full Text] [Related]
30. Linkage of benign familial infantile convulsions to chromosome 16p12-q12 suggests allelism to the infantile convulsions and choreoathetosis syndrome.
Caraballo R; Pavek S; Lemainque A; Gastaldi M; Echenne B; Motte J; Genton P; Cersósimo R; Humbertclaude V; Fejerman N; Monaco AP; Lathrop MG; Rochette J; Szepetowski P
Am J Hum Genet; 2001 Mar; 68(3):788-94. PubMed ID: 11179027
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. [Diurnal and nocturnal paroxysmal dyskinesia in young children: a new entity?].
de Saint-Martin A; Badinand N; Picard F; Fischbach M; Challamel MJ; Marescaux C; Hirsch E
Rev Neurol (Paris); 1997 May; 153(4):262-7. PubMed ID: 9296145
[TBL] [Abstract][Full Text] [Related]
33. Nocturnal frontal lobe epilepsy. A clinical and polygraphic overview of 100 consecutive cases.
Provini F; Plazzi G; Tinuper P; Vandi S; Lugaresi E; Montagna P
Brain; 1999 Jun; 122 ( Pt 6)():1017-31. PubMed ID: 10356056
[TBL] [Abstract][Full Text] [Related]
34. Paroxysmal dyskinesias revisited: a review of 500 genetically proven cases and a new classification.
Erro R; Sheerin UM; Bhatia KP
Mov Disord; 2014 Aug; 29(9):1108-16. PubMed ID: 24963779
[TBL] [Abstract][Full Text] [Related]
35. Autosomal dominant nocturnal frontal lobe epilepsy--a critical overview.
Combi R; Dalprà L; Tenchini ML; Ferini-Strambi L
J Neurol; 2004 Aug; 251(8):923-34. PubMed ID: 15316796
[TBL] [Abstract][Full Text] [Related]
36. Association of infantile convulsions with paroxysmal dyskinesias (ICCA syndrome): confirmation of linkage to human chromosome 16p12-q12 in a Chinese family.
Lee WL; Tay A; Ong HT; Goh LM; Monaco AP; Szepetowski P
Hum Genet; 1998 Nov; 103(5):608-12. PubMed ID: 9860304
[TBL] [Abstract][Full Text] [Related]
37. Genetic Links to Episodic Movement Disorders: Current Insights.
Garg D; Mohammad S; Shukla A; Sharma S
Appl Clin Genet; 2023; 16():11-30. PubMed ID: 36883047
[TBL] [Abstract][Full Text] [Related]
38. Paroxysmal movement disorders - practical update on diagnosis and management.
De Gusmao CM; Silveira-Moriyama L
Expert Rev Neurother; 2019 Sep; 19(9):807-822. PubMed ID: 31353980
[No Abstract] [Full Text] [Related]
39.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
40.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]