BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

155 related articles for article (PubMed ID: 17900292)

  • 1. Autosomal dominant nocturnal frontal lobe epilepsy with a mutation in the CHRNB2 gene.
    Díaz-Otero F; Quesada M; Morales-Corraliza J; Martínez-Parra C; Gómez-Garre P; Serratosa JM
    Epilepsia; 2008 Mar; 49(3):516-20. PubMed ID: 17900292
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Evidence for S284L mutation of the CHRNA4 in a white family with autosomal dominant nocturnal frontal lobe epilepsy.
    Rozycka A; Skorupska E; Kostyrko A; Trzeciak WH
    Epilepsia; 2003 Aug; 44(8):1113-7. PubMed ID: 12887446
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Autosomal dominant nocturnal frontal lobe epilepsy: an electroclinical study of a Norwegian family with ten affected members.
    Nakken KO; Magnusson A; Steinlein OK
    Epilepsia; 1999 Jan; 40(1):88-92. PubMed ID: 9924907
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Further evidence of genetic heterogeneity in families with autosomal dominant nocturnal frontal lobe epilepsy.
    De Marco EV; Gambardella A; Annesi F; Labate A; Carrideo S; Forabosco P; Civitelli D; Candiano IC; Tarantino P; Annesi G; Quattrone A
    Epilepsy Res; 2007 Apr; 74(1):70-3. PubMed ID: 17324557
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The identification of a novel mutation of nicotinic acetylcholine receptor gene CHRNB2 in a Chinese patient: Its possible implication in non-familial nocturnal frontal lobe epilepsy.
    Liu H; Lu C; Li Z; Zhou S; Li X; Ji L; Lu Q; Lv R; Wu L; Ma X
    Epilepsy Res; 2011 Jun; 95(1-2):94-9. PubMed ID: 21497487
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A major role of the nicotinic acetylcholine receptor gene CHRNA2 in autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) is unlikely.
    Gu W; Bertrand D; Steinlein OK
    Neurosci Lett; 2007 Jul; 422(1):74-6. PubMed ID: 17602836
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Autosomal dominant nocturnal frontal lobe epilepsy. A video-polysomnographic and genetic appraisal of 40 patients and delineation of the epileptic syndrome.
    Oldani A; Zucconi M; Asselta R; Modugno M; Bonati MT; Dalprà L; Malcovati M; Tenchini ML; Smirne S; Ferini-Strambi L
    Brain; 1998 Feb; 121 ( Pt 2)():205-23. PubMed ID: 9549500
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Phenotypic comparison of two Scottish families with mutations in different genes causing autosomal dominant nocturnal frontal lobe epilepsy.
    McLellan A; Phillips HA; Rittey C; Kirkpatrick M; Mulley JC; Goudie D; Stephenson JB; Tolmie J; Scheffer IE; Berkovic SF; Zuberi SM
    Epilepsia; 2003 Apr; 44(4):613-7. PubMed ID: 12681012
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Nocturnal frontal lobe epilepsy with paroxysmal arousals due to CHRNA2 loss of function.
    Conti V; Aracri P; Chiti L; Brusco S; Mari F; Marini C; Albanese M; Marchi A; Liguori C; Placidi F; Romigi A; Becchetti A; Guerrini R
    Neurology; 2015 Apr; 84(15):1520-8. PubMed ID: 25770198
    [TBL] [Abstract][Full Text] [Related]  

  • 11. CHRNB2 is the second acetylcholine receptor subunit associated with autosomal dominant nocturnal frontal lobe epilepsy.
    Phillips HA; Favre I; Kirkpatrick M; Zuberi SM; Goudie D; Heron SE; Scheffer IE; Sutherland GR; Berkovic SF; Bertrand D; Mulley JC
    Am J Hum Genet; 2001 Jan; 68(1):225-31. PubMed ID: 11104662
    [TBL] [Abstract][Full Text] [Related]  

  • 12. SER252PHE and 776INS3 mutations in the CHRNA4 gene are rare in the Italian ADNFLE population.
    Tenchini ML; Duga S; Bonati MT; Asselta R; Oldani A; Zucconi M; Malcovati M; Dalprà L; Ferini-Strambi L
    Sleep; 1999 Aug; 22(5):637-9. PubMed ID: 10450598
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1.
    Gambardella A; Annesi G; De Fusco M; Patrignani A; Aguglia U; Annesi F; Pasqua AA; Spadafora P; Oliveri RL; Valentino P; Zappia M; Ballabio A; Casari G; Quattrone A
    Neurology; 2000 Nov; 55(10):1467-71. PubMed ID: 11094099
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. [Mutational analysis of CHRNB2 and CHRNA2 genes in southern Chinese population with autosomal dominant nocturnal frontal lobe epilepsy].
    Chen ZH; Zhai QX; Gui J; Zhang YX; Guo YX; Ding J; Hao Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Feb; 28(1):14-8. PubMed ID: 21287502
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutational analysis of nicotinic acetylcholine receptor beta2 subunit gene (CHRNB2) in a representative cohort of Italian probands affected by autosomal dominant nocturnal frontal lobe epilepsy.
    Duga S; Asselta R; Bonati MT; Malcovati M; Dalprà L; Oldani A; Zucconi M; Ferini-Strambi L; Tenchini ML
    Epilepsia; 2002 Apr; 43(4):362-4. PubMed ID: 11952766
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutations in familial nocturnal frontal lobe epilepsy might be associated with distinct neurological phenotypes.
    Steinlein OK; Hoda JC; Bertrand S; Bertrand D
    Seizure; 2012 Mar; 21(2):118-23. PubMed ID: 22036597
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Autosomal dominant nocturnal frontal lobe epilepsy and mild memory impairment associated with CHRNB2 mutation I312M in the neuronal nicotinic acetylcholine receptor.
    Cho YW; Yi SD; Lim JG; Kim DK; Motamedi GK
    Epilepsy Behav; 2008 Aug; 13(2):361-5. PubMed ID: 18534914
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.