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.
24. Clinical and electroencephalographic study of first-degree relatives and probands with juvenile myoclonic epilepsy. Jayalakshmi SS; Mohandas S; Sailaja S; Borgohain R Seizure; 2006 Apr; 15(3):177-83. PubMed ID: 16495091 [TBL] [Abstract][Full Text] [Related]
25. Long-term disability and prognosis in dentatorubral-pallidoluysian atrophy: a correlation with CAG repeat length. Hasegawa A; Ikeuchi T; Koike R; Matsubara N; Tsuchiya M; Nozaki H; Homma A; Idezuka J; Nishizawa M; Onodera O Mov Disord; 2010 Aug; 25(11):1694-700. PubMed ID: 20589872 [TBL] [Abstract][Full Text] [Related]
26. Analysis of CAG repeats in SCA1, SCA2, SCA3, SCA6, SCA7 and DRPLA loci in spinocerebellar ataxia patients and distribution of CAG repeats at the SCA1, SCA2 and SCA6 loci in nine ethnic populations of eastern India. Basu P; Chattopadhyay B; Gangopadhaya PK; Mukherjee SC; Sinha KK; Das SK; Roychoudhury S; Majumder PP; Bhattacharyya NP Hum Genet; 2000 Jun; 106(6):597-604. PubMed ID: 10942107 [TBL] [Abstract][Full Text] [Related]
27. A new EF-hand containing gene EFHC2 on Xp11.4: tentative evidence for association with juvenile myoclonic epilepsy. Gu W; Sander T; Heils A; Lenzen KP; Steinlein OK Epilepsy Res; 2005; 66(1-3):91-8. PubMed ID: 16112844 [TBL] [Abstract][Full Text] [Related]
29. DNA analysis in hereditary dentatorubral-pallidoluysian atrophy: correlation between CAG repeat length and phenotypic variation and the molecular basis of anticipation. Komure O; Sano A; Nishino N; Yamauchi N; Ueno S; Kondoh K; Sano N; Takahashi M; Murayama N; Kondo I Neurology; 1995 Jan; 45(1):143-9. PubMed ID: 7824105 [TBL] [Abstract][Full Text] [Related]
30. Structural insights of novel mutational frames in Bromodomain Containing-2 gene (BRD2) in juvenile myoclonic epilepsy: bed, bench, and laptop profiles. Kothapalli J; Prasad Uppu V; Munikumar M; Kshirsagar SV; Afshan Jabeen S; Sivanarayana G Epilepsy Behav; 2023 Jul; 144():109282. PubMed ID: 37276801 [TBL] [Abstract][Full Text] [Related]
31. Dentatorubral pallidoluysian atrophy in South Wales. Wardle M; Majounie E; Williams NM; Rosser AE; Morris HR; Robertson NP J Neurol Neurosurg Psychiatry; 2008 Jul; 79(7):804-7. PubMed ID: 17965145 [TBL] [Abstract][Full Text] [Related]
32. Elongated CAG repeats of the B37 gene in a Danish family with dentato-rubro-pallido-luysian atrophy. Nørremølle A; Nielsen JE; Sørensen SA; Hasholt L Hum Genet; 1995 Mar; 95(3):313-8. PubMed ID: 7868125 [TBL] [Abstract][Full Text] [Related]
33. Lack of association between the prothrombin rs1799963 polymorphism and juvenile myoclonic epilepsy. Born JP; Santos BP; Secolin R; Gameleira FT; Andrade TG; Machado LC; Gitaí LL; Gitaí DL Arq Neuropsiquiatr; 2015 Apr; 73(4):289-92. PubMed ID: 25992517 [TBL] [Abstract][Full Text] [Related]
34. Confirmatory evidence for an association of the connexin-36 gene with juvenile myoclonic epilepsy. Hempelmann A; Heils A; Sander T Epilepsy Res; 2006 Oct; 71(2-3):223-8. PubMed ID: 16876983 [TBL] [Abstract][Full Text] [Related]