BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

225 related articles for article (PubMed ID: 19577488)

  • 1. The 1674+11C>T polymorphism of CHRNA4 is associated with juvenile myoclonic epilepsy.
    Rozycka A; Steinborn B; Trzeciak WH
    Seizure; 2009 Oct; 18(8):601-3. PubMed ID: 19577488
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Possible association of a silent polymorphism in the neuronal nicotinic acetylcholine receptor subunit alpha4 with common idiopathic generalized epilepsies.
    Steinlein O; Sander T; Stoodt J; Kretz R; Janz D; Propping P
    Am J Med Genet; 1997 Jul; 74(4):445-9. PubMed ID: 9259383
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Association of the neuronal nicotinic acetylcholine receptor subunit alpha4 polymorphisms with febrile convulsions.
    Chou IC; Lee CC; Huang CC; Wu JY; Tsai JJ; Tsai CH; Tsai FJ
    Epilepsia; 2003 Aug; 44(8):1089-93. PubMed ID: 12887442
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. A novel mutation of the nicotinic acetylcholine receptor gene CHRNA4 in sporadic nocturnal frontal lobe epilepsy.
    Chen Y; Wu L; Fang Y; He Z; Peng B; Shen Y; Xu Q
    Epilepsy Res; 2009 Feb; 83(2-3):152-6. PubMed ID: 19058950
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Association of idiopathic generalized epilepsy with polymorphisms in the neuronal nicotinic acetylcholine receptor subunits.
    Lee CC; Chou IC; Tsai CH; Wan L; Shu YA; Tsai Y; Li TC; Tsai FJ
    J Clin Lab Anal; 2007; 21(2):67-70. PubMed ID: 17385675
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Lack of association between rs211037 of the GABRG2 gene and juvenile myoclonic epilepsy in Brazilian population.
    Gitaí LL; de Almeida DH; Born JP; Gameleira FT; de Andrade TG; Machado LC; Gitaí DL
    Neurol India; 2012; 60(6):585-8. PubMed ID: 23287319
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Failure to replicate association between the gene for the neuronal nicotinic acetylcholine receptor alpha 4 subunit (CHRNA4) and IGE.
    Chioza B; Goodwin H; Blower J; McCormick D; Nashef L; Asherson P; Makoff AJ
    Am J Med Genet; 2000 Dec; 96(6):814-6. PubMed ID: 11121188
    [TBL] [Abstract][Full Text] [Related]  

  • 10. PER2 rs2304672, CLOCK rs1801260, and PER3 rs57875989 polymorphisms are not associated with juvenile myoclonic epilepsy.
    Santos B; Marques T; Malta M; Gameleira F; Secolin R; Andrade T; Gitaí L; Gitaí D
    Epilepsy Behav; 2014 Jul; 36():82-5. PubMed ID: 24892753
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Juvenile myoclonic epilepsy and idiopathic photosensitive occipital lobe epilepsy: is there overlap?
    Taylor I; Marini C; Johnson MR; Turner S; Berkovic SF; Scheffer IE
    Brain; 2004 Aug; 127(Pt 8):1878-86. PubMed ID: 15201194
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Association of serotonin transporter gene (5HTT) polymorphism and juvenile myoclonic epilepsy: a case-control study.
    Esmail EH; Labib DM; Rabie WA
    Acta Neurol Belg; 2015 Sep; 115(3):247-51. PubMed ID: 25481722
    [TBL] [Abstract][Full Text] [Related]  

  • 13. DNA variants in coding region of EFHC1: SNPs do not associate with juvenile myoclonic epilepsy.
    Bai D; Bailey JN; Durón RM; Alonso ME; Medina MT; Martínez-Juárez IE; Suzuki T; Machado-Salas J; Ramos-Ramírez R; Tanaka M; Ortega RH; López-Ruiz M; Rasmussen A; Ochoa A; Jara-Prado A; Yamakawa K; Delgado-Escueta AV
    Epilepsia; 2009 May; 50(5):1184-90. PubMed ID: 18823326
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Juvenile myoclonic epilepsy subsyndromes: family studies and long-term follow-up.
    Martínez-Juárez IE; Alonso ME; Medina MT; Durón RM; Bailey JN; López-Ruiz M; Ramos-Ramírez R; León L; Pineda G; Castroviejo IP; Silva R; Mija L; Perez-Gosiengfiao K; Machado-Salas J; Delgado-Escueta AV
    Brain; 2006 May; 129(Pt 5):1269-80. PubMed ID: 16520331
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Exclusion of linkage of nine neuronal nicotinic acetylcholine receptor subunit genes expressed in brain in autosomal dominant nocturnal frontal lobe epilepsy in four unrelated families.
    Bonati MT; Combi R; Asselta R; Duga S; Malcovati M; Oldani A; Zucconi M; Ferini-Strambi L; Dalprà L; Tenchini ML
    J Neurol; 2002 Aug; 249(8):967-74. PubMed ID: 12195439
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel mutation of CHRNA4 responsible for autosomal dominant nocturnal frontal lobe epilepsy.
    Hirose S; Iwata H; Akiyoshi H; Kobayashi K; Ito M; Wada K; Kaneko S; Mitsudome A
    Neurology; 1999 Nov; 53(8):1749-53. PubMed ID: 10563623
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutations in the GABRA1 and EFHC1 genes are rare in familial juvenile myoclonic epilepsy.
    Ma S; Blair MA; Abou-Khalil B; Lagrange AH; Gurnett CA; Hedera P
    Epilepsy Res; 2006 Oct; 71(2-3):129-34. PubMed ID: 16839746
    [TBL] [Abstract][Full Text] [Related]  

  • 19. No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy.
    Mumoli L; Tarantino P; Michelucci R; Bianchi A; Labate A; Franceschetti S; Marini C; Striano P; Gagliardi M; Ferlazzo E; Sofia V; Pennese L; Annesi G; Aguglia U; Guerrini R; Zara F; Gambardella A;
    Epilepsia; 2015 Apr; 56(4):e40-3. PubMed ID: 25752200
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Evaluation of a putative major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q14.
    Sander T; Schulz H; Vieira-Saeker AM; Bianchi A; Sailer U; Bauer G; Scaramelli A; Wienker TF; Saar K; Reis A; Janz D; Epplen JT; Riess O
    Am J Med Genet; 1999 Apr; 88(2):182-7. PubMed ID: 10206240
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.