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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

125 related articles for article (PubMed ID: 21439911)

  • 1. A polymorphism in CALHM1 is associated with temporal lobe epilepsy.
    Lv RJ; He JS; Fu YH; Shao XQ; Wu LW; Lu Q; Jin LR; Liu H
    Epilepsy Behav; 2011 Apr; 20(4):681-5. PubMed ID: 21439911
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic association between CALHM1, 2, and 3 polymorphisms and Alzheimer's disease in a Japanese population.
    Shibata N; Kuerban B; Komatsu M; Ohnuma T; Baba H; Arai H
    J Alzheimers Dis; 2010; 20(2):417-21. PubMed ID: 20164573
    [TBL] [Abstract][Full Text] [Related]  

  • 3. No association between polymorphisms in the calcium homeostasis modulator 1 gene and mesial temporal lobe epilepsy risk in a Chinese population.
    Li X; Wang Y; Gu J; Meng Q; Gao Y; Zhao H; Yin Z
    Seizure; 2014 Mar; 23(3):231-3. PubMed ID: 24326043
    [TBL] [Abstract][Full Text] [Related]  

  • 4. CALHM1 variant is not associated with Alzheimer's disease among Asians.
    Tan EK; Ho P; Cheng SY; Yih Y; Li HH; Fook-Chong S; Lee WL; Zhao Y
    Neurobiol Aging; 2011 Mar; 32(3):546.e11-2. PubMed ID: 19545933
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Variants of the genes encoding AQP4 and Kir4.1 are associated with subgroups of patients with temporal lobe epilepsy.
    Heuser K; Nagelhus EA; Taubøll E; Indahl U; Berg PR; Lien S; Nakken S; Gjerstad L; Ottersen OP
    Epilepsy Res; 2010 Jan; 88(1):55-64. PubMed ID: 19864112
    [TBL] [Abstract][Full Text] [Related]  

  • 6. No association between CALHM1 and risk for Alzheimer dementia in a Belgian population.
    Sleegers K; Brouwers N; Bettens K; Engelborghs S; van Miegroet H; De Deyn PP; Van Broeckhoven C
    Hum Mutat; 2009 Apr; 30(4):E570-4. PubMed ID: 19191332
    [TBL] [Abstract][Full Text] [Related]  

  • 7. No association between CALHM1 polymorphism and Alzheimer's disease risk in a Hungarian population.
    Fehér A; Juhász A; Rimanóczy A; Pákáski M; Kálmán J; Janka Z
    Psychiatr Genet; 2011 Oct; 21(5):249-52. PubMed ID: 21378601
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Lack of implication for CALHM1 P86L common variation in Italian patients with early and late onset Alzheimer's disease.
    Nacmias B; Tedde A; Bagnoli S; Lucenteforte E; Cellini E; Piaceri I; Guarnieri BM; Bessi V; Bracco L; Sorbi S
    J Alzheimers Dis; 2010; 20(1):37-41. PubMed ID: 20164602
    [TBL] [Abstract][Full Text] [Related]  

  • 9. CALHM1 P86L polymorphism is associated with late-onset Alzheimer's disease in a recessive model.
    Boada M; Antúnez C; López-Arrieta J; Galán JJ; Morón FJ; Hernández I; Marín J; Martínez-Lage P; Alegret M; Carrasco JM; Moreno C; Real LM; González-Pérez A; Tárraga L; Ruiz A
    J Alzheimers Dis; 2010; 20(1):247-51. PubMed ID: 20164592
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Serotonin transporter gene (5-Htt): association analysis with temporal lobe epilepsy.
    Manna I; Labate A; Gambardella A; Forabosco P; La Russa A; Le Piane E; Aguglia U; Quattrone A
    Neurosci Lett; 2007 Jun; 421(1):52-6. PubMed ID: 17548158
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Effect of apolipoprotein ε4 allele on hippocampal and brain volume in intractable temporal lobe epilepsy.
    Busch RM; Floden D; Lineweaver TT; Chapin JS; Unnwongse K; Wehner T; Diaz-Arrastia R; Najm IM
    Epilepsy Behav; 2011 May; 21(1):88-90. PubMed ID: 21317045
    [TBL] [Abstract][Full Text] [Related]  

  • 12. CALHM1 P86L polymorphism modulates CSF Aβ levels in cognitively healthy individuals at risk for Alzheimer's disease.
    Koppel J; Campagne F; Vingtdeux V; Dreses-Werringloer U; Ewers M; Rujescu D; Hampel H; Gordon ML; Christen E; Chapuis J; Greenwald BS; Davies P; Marambaud P
    Mol Med; 2011; 17(9-10):974-9. PubMed ID: 21629967
    [TBL] [Abstract][Full Text] [Related]  

  • 13. No major clinical impact of Val66Met BDNF gene polymorphism on temporal lobe epilepsy.
    Bragatti JA; Schenkel LC; Torres CM; Manfro GG; Blaya C; Souza AC; Souza DO; Saraiva-Pereira ML; Jardim LB; Leistner-Segal S; Bianchin MM
    Epilepsy Res; 2010 Feb; 88(2-3):108-11. PubMed ID: 19896331
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Association between somatostatin gene polymorphisms and sporadic Alzheimer's disease in Chinese population.
    Xue S; Jia L; Jia J
    Neurosci Lett; 2009 Nov; 465(2):181-3. PubMed ID: 19733630
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Temporal lobe epilepsy and matrix metalloproteinase 9: a tempting relation but negative genetic association.
    Heuser K; Hoddevik EH; Taubøll E; Gjerstad L; Indahl U; Kaczmarek L; Berg PR; Lien S; Nagelhus EA; Ottersen OP
    Seizure; 2010 Jul; 19(6):335-8. PubMed ID: 20605480
    [TBL] [Abstract][Full Text] [Related]  

  • 16. GABBR1 gene polymorphism(G1465A)isassociated with temporal lobe epilepsy.
    Xi B; Chen J; Yang L; Wang W; Fu M; Wang C
    Epilepsy Res; 2011 Sep; 96(1-2):58-63. PubMed ID: 21621395
    [TBL] [Abstract][Full Text] [Related]  

  • 17. GABA receptor 1 polymorphism (G1465A) and temporal lobe epilepsy.
    Salzmann A; Moulard B; Crespel A; Baldy-Moulinier M; Buresi C; Malafosse A
    Epilepsia; 2005 Jun; 46(6):931-3. PubMed ID: 15946333
    [TBL] [Abstract][Full Text] [Related]  

  • 18. ApoE epsilon4 allele and disease duration affect verbal learning in mild temporal lobe epilepsy.
    Gambardella A; Aguglia U; Chifari R; Labate A; Manna I; Serra P; Romeo N; Sibilia G; Lepiane E; Russa AL; Ventura P; Cittadella R; Sasanelli F; Colosimo E; Leggio U; Zappia M; Quattrone A
    Epilepsia; 2005 Jan; 46(1):110-7. PubMed ID: 15660776
    [TBL] [Abstract][Full Text] [Related]  

  • 19. ApoE epsilon4 is not associated with posictal confusion in patients with mesial temporal lobe epilepsy with hippocampal sclerosis.
    Kauffman MA; Pereira-de-Silva N; Consalvo D; Kochen S
    Epilepsy Res; 2009 Aug; 85(2-3):311-3. PubMed ID: 19375284
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Serotonin transporter gene (5HTT) polymorphisms and temporal lobe epilepsy.
    Schenkel LC; Bragatti JA; Torres CM; Martin KC; Gus-Manfro G; Leistner-Segal S; Bianchin MM
    Epilepsy Res; 2011 Jun; 95(1-2):152-7. PubMed ID: 21498047
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.